Document jyQ7LGrkDVjrXqgrndyLDDVxZ
IN THE 3 OTH JUDICIAL CIRCUIT COURT FOR ST. CLAIR COUNTY, ALABAMA PELL CITY DIVISION
THOMAS C. DYER, ET AL, Plaintiff,
vs . MONSANTO COMPANY, ET AL,
Defendant.
) ) ) ) ) NO. CV-93-250 ) ) ) )
Consolidated For Discovery With
SHELTER COVE MANAGEMENT, INC., ET AL,
Plaintiff,
) ) ) )
vs . MONSANTO COMPANY, ET AL,
) NO. CV 94-50-PH ) )
Defendant.
)
DEPOSITION OF MICHAEL A. PIERLE Taken on behalf of the Plaintiff
October 28, 1998
REPORTER: Kevin J. Weichman, CSR-RPR No. 084-003189
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INDEX
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EXAMINATION
2 QUESTIONS BY:
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MR. GRAMMAS .............
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INDEX
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Plaintiff' s 1 ...................................................................................................
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Plaintiff's 9 ................................................................................................... 138
10 Plaintiff's 10................................................................................................... 150
Plaintiff's 11................................................................................................... 156
11 Plaintiff's 12................................................................................................... 167
Plaintiff's 13................................................................................................... 167
12 Plaintiff's 14................................................................................................... 199
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1 IN THE 3 OTH JUDICIAL CIRCUIT COURT FOR
ST. CLAIR COUNTY, ALABAMA 2 PELL CITY DIVISION
3
THOMAS C. DYER, ET AL,
)
4)
Plaintiff,
)
5
vs .
) NO. CV-93-250
6)
MONSANTO COMPANY, ET AL,
)
7)
Defendant.
)
8
Consolidated For Discovery With 9
SHELTER COVE MANAGEMENT,
)
10 INC., ET AL,
)
)
11
Plaintiff,
)
12 vs .
) NO. CV 94-50-PH
)
13 MONSANTO COMPANY, ET AL,
)
)
14
Defendant.
)
15
16
17
18 THE DEPOSITION OF MICHAEL PIERLE, produced,
19 sworn, and examined on behalf of the Plaintiff, on
20 Wednesday, October 28, 1998, at 9:15 a.m., at the
21 offices of Taylor & Schroeder Reporting & Video, 7494
22 Ethel Avenue, St. Louis, Missouri, before KEVIN J.
23 WEICHMAN, a Certified Shorthand Reporter, Registered 24 Professional Reporter, and Notary Public within and for
25 the County of St. Louis, State of Missouri.
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1 APPEARANCES 2 3 ON BEHALF OF THE PLAINTIFF4 Peter A. Grammas, Esq. 5 E. Clayton Lowe, Jr., Esq. 6 Burr Sc Forman, L.L.P. 7 3100 SouthTrust Tower 8 420 North 20th Street 9 Birmingham, Alabama 35203 10 MAIN: (205) 251-3000 11 FAX: (205) 458-5100 12 13 ON BEHALF OF THE DEFENDANT: 14 Adam K. Peck, Esq. 15 Lightfoot, Franklin & White, L.L.C. 16 300 Financial Center 17 505 20th Street North 18 Birmingham, Alabama 35203 19 MAIN: (205) 581-0700 20 FAX: (205) 581-0799 21 22 Michael E. Kelly 23 Smith, Helms, Mulliss & Moore 24 300 N. Greene Street, Suite 1400 25 Greensboro, NC 27401
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1 IT IS STIPULATED AND AGREED by and between 2 counsel for the Plaintiff and counsel for the Defendant 3 that the deposition of MICHAEL PIERLE may be taken 4 pursuant to and in accordance with the provisions of 5 the Federal Rules of Civil Procedure pertaining to such 6 depositions, by and on behalf of the Plaintiff, on 7 Wednesday, October 28, 1998, at the offices of Taylor & 8 Schroeder Reporting & Video, 7494 Ethel Avenue, St. 9 Louis, Missouri, before KEVIN J. WEICHMAN, a Certified 10 Shorthand Reporter and Notary Public within and for the 11 County of St. Louis, State of Missouri. 12 13 14 MICHAEL PIERLE, 15 of lawful age, being produced, sworn, and examined on 16 the part of the Plaintiff, after answering "I do" to 17 the oath administered by the court reporter, deposes 18 and says: 19 MR. PECK: Usual stipulations? 20 MR. GRAMMAS: Does he want to read and sign? 21 MR. PECK: Do you want to read and sign, Mike? 22 MR. LOWE: We'd prefer him to. 23 (PIERLE EXHIBIT NOS. 1 THROUGH 3 WERE FIRST DULY 24 MARKED, RECEIVED AND MADE A PART OF THE RECORD.) 25 DIRECT EXAMINATION
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1 BY MR. GRAMMAS: 2 Q. Could you state your full name for the record, 3 please. 4 A. Michael Anthony Pierle. 5 Q. And where do you currently live, Mr. Pierle? 6 A. 801 Greenwich Green Lane in Town and Country, 7 Missouri. 8 Q. Is that near St. Louis? 9 A. It is. 10 Q. And what is your current position? 11 A. Vice president of environmental safety and 12 health for Solutia. 13 Q. How long have you held that position? 14 A. Since the company was created the 1st of 15 September, 1997. 16 Q. If I understand from prior testimony, Solutia 17 was a company that Monsanto had spun off? 18 A. That's correct. 19 Q. And all of the people -- well, not all, but a 20 significant number of people making up employees of 21 Solutia currently were employed by Monsanto before 22 September of 1997? 23 A. That's correct. 24 Q. There wasn't a big shift in employees and that 25 type stuff, I mean, it was really basically a name
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1 change and what was part of a division of Monsanto is 2 now a separate company? 3 A. That's correct. 4 Q. And what did you do, sir, before you were 5 employed as the vice president of environmental safety 6 and health for Solutia? 7 A. I virtually had the same position as vice 8 president of environmental safety and health for 9 Monsanto Company. 10 Q. And how long have you -- how long did you hold 11 that position? 12 A. I began that position somewhere around April 13 or May of 1991. 14 Q. And did your job responsibilities change from 15 Solutia -- once you became employed by Solutia, were 16 they basically the same as your job responsibilities 17 when you were employed by Monsanto? 18 A. They're basically the same. 19 Q. I was on the Internet for Monsanto and what I 20 observed on the Internet was a -- I guess a "bio," for 21 lack of a better word, on you. Is that an accurate 22 description of what I've just shown you now as 23 Plaintiff's Exhibit No. 1? 24 A. Is the content accurate; is that what you are 25 asking?
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1 Q. Is this a bio of your -- basically a general 2 description of your background as far as education and 3 employment? 4 A. Yes. 5 Q. And before we start, I asked you to look over 6 that and I asked you if it was all true and accurate, 7 and you noticed that there may have been a couple 8 things that weren't quite correct. Could you clarify 9 what you believe may need some further discussion. 10 A. Yes. In the second-to-last paragraph on the 11 first page, it indicates that I'm a member of the board 12 of directors of the Monsanto Fund. That is incorrect. 13 It should be the Solutia Fund. And in the sentence 14 following that, which is: "He is chairman of the 15 National Wildlife Federation's Corporate Conservation 16 Council," that council no longer exists. So I'm no 17 longer in that capacity. 18 Q. Before September 1997, were you a member of 19 the board of directors of the Monsanto Fund? 20 A Yes. 21 Q. So this is not necessarily incorrect, it's 22 just incomplete in that it should also state in here 23 that you're now a board of director for the Solutia 24 Fund? 25 A. That's a fair point. You had started and said
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1 that was off of the Monsanto Internet. It's quite 2 confusing. 3 Q. Yeah. What I did, I typed in "Monsanto" and 4 some things from Monsanto came up and some things for 5 Solutia came up. This apparently has a Solutia 6 Internet address on it. 7 A. I would have thought so. 8 Q. And it's like www.solutia.com, et cetera, et 9 cetera. But I pulled this up off of the Monsanto site. 10 Apparently they're interrelated. 11 All right. Let's talk a little bit, then, 12 about some of the things contained in this Plaintiff's 13 Exhibit 1. Your educational history, could you just 14 briefly give that to me. 15 A. I graduated with a civil engineering degree 16 from Purdue University in 1966 and I received a 17 master's degree in engineering from Washington 18 University in 1971. And then in addition to those 19 formal degrees, I attended two sort of executive 20 management programs at the University of Texas and at 21 Stanford. 22 Q. Did you say your master's was in engineering 23 also? 24 A. Yes. 25 Q. And what were these executive -- how did you
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1 describe them? 2 A. They're basically executive management 3 sessions. Probably the best description is they are 4 sort of mini-master's of business programs. But 5 there's no degree associated with them. 6 Q. Is it more of a seminar or course work? 7 A. It is -- it's basically course work. 8 Q. And how long did it take you to complete the 9 courses? 10 A. Well, the one program in Texas, I think, ran 11 four or five weeks and the Stanford program ran eight 12 weeks. 13 Q. And you did that continuously, you took time 14 away from Monsanto? 15 A. Yes. 16 Q. When did you attend these management - 17 A. I think the exact dates are on the exhibit. 18 The Texas program was in the '80s and the Stanford 19 program was in 1990. 20 Q. Because I didn't see -- and I've read this. I 21 didn't see those two mentioned anywhere in this 22 exhibit. 23 A. I thought that they were mentioned at the 24 bottom of it. 25 Q. You're right, they are. I'm sorry.
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1 Once you got your first civil engineering 2 degree from Purdue in 1966, where did you begin work? 3 A. I joined the Monsanto Company. 4 Q. And what was the reason for you going to 5 Monsanto? 6 A. Best job offer that I had at the time. 7 Q. I mean, did you have any particular ties to 8 Monsanto, parents work there, friends work there, 9 anything like that? 10 A. None. 11 Q. And what did you start out as at Monsanto in 12 1966? 13 A. I started as basically a beginning engineer 14 position with the company. 15 Q. And what types of things would you do, did you 16 do? 17 A. I was in an environmental group at the time 18 that was basically doing environmental monitoring, 19 primarily air and water work. 20 Q. And what was it about a civil engineering 21 degree that qualified you to take that position? 22 A. In the civil engineering program at Purdue, 23 there are several elective areas, one of which was 24 environmental engineering, and I had taken a 25 concentrated set of courses in that portion of civil
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1 engineering; and that as much as anything sort of 2 introduced me to the area and created interest and I 3 was able to, you know, find employment initially in 4 that field. 5 Q. Now, what types of things would you do as far 6 as monitoring environmental activities relating to air 7 and water for Monsanto at that time when you first 8 began employment with them? 9 A. Basically the work was looking at sampling 10 systems, developing certain sampling systems for water. 11 We were primarily concentrated there around 12 measurements of phenol and something called "COD," or 13 chemical oxygen demand. And in the air area, most of 14 the work that we were doing was sulfur dioxide 15 emissions primarily associated with power plants. 16 Q. Did any of your work involve studying the 17 impact that Monsanto's manufacturing operations had on 18 the environment? 19 A. You know, at that time we were looking at 20 certain, you know, effluents and discharges. You know, 21 to some extent that's looking at releases, but not 22 ultimate impact in the environment. 23 Q. Was there a division at Monsanto at that time, 24 when you first joined Monsanto in 1966, that was 25 charged with the responsibility of looking to see what
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1 impacts Monsanto's manufacturing operations had on the
2 environment ? 3 A. I don't know whether -- we're dealing with 4 word definition here, you know, so I don't know what 5 you really mean by "impact on the environment." 6 Q. Well, what I mean by that is if you're 7 manufacturing chemicals and you're discharging 8 chemicals, either through permits or otherwise, into, 9 say, bodies of water, what impact those chemicals may 10 have on aquatic life, on the river systems, on people 11 who swim, boat, fishing, on people who eat the fish, 12 that type stuff? 13 A. My recollection of most of the plants at that 14 time had persons or people who were looking at 15 discharges in accordance with regulatory permits, 16 primarily at the state level, and determining 17 conformance with those. Again, I think the general 18 assumption there was that the discharges in accordance 19 with allowable permits and releases were acceptable 20 to -- were acceptable to the environment. 21 Q. Do I understand your testimony correctly, 22 then, in that you're saying that there was not a 23 particular division or department here in St. Louis 24 that oversaw all of the plants that Monsanto had around 25 the country, dealing with potential impacts of its
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1 plant operations on the environment?
2 A. I don't know. I mean, in looking back at that
3 time, you know, my position at that point in time was
4 fairly narrow as a new engineer and I really didn't 5 have at that time a total understanding of what the 6 company's efforts and programs and their resources 7 were. 8 Q. But the position you held as an environmental 9 monitor -- and I don't know if that's a correct job 10 description, maybe it is, maybe it's not -- didn't deal 11 with studying the impacts of chemicals being left in 12 the environment and what impacts that would have, if at 13 all, on the community? 14 A. I think I've described what it is, and at that 15 time the sense was if you're discharging things within 16 your permit limits, that that's what constituted 17 acceptable protection in the environment and the 18 community. 19 Q. What permits in 1966 did Monsanto hold at its 20 Anniston plant in Anniston, Alabama, that gave it the 21 right to discharge PCBs into Snow Creek, Choccolocco 22 Creek? 23 A. I was not familiar with the plant at that 24 time, so I don't know what their factual permitted 25 situation was.
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1 Q. Are you aware of any permits at all that
2 Monsanto ever had at any plant that allowed it to dump 3 PCBs into a river system? 4 A. As I recall, the structure of the permitted 5 systems is that back at state levels, and then when 6 federal permits came in in the '70s, is that the 7 permits dealt with what was restricted; things that 8 were not included were not unrestricted. 9 Q. Things that were not included were not 10 unrestricted. That's a triple negative. I'm trying to 11 figure out what that means. If something was not 12 included on a permit, Monsanto could dump as much of it 13 as it wanted into the river system? 14 A. I think that's the right legal interpretation. 15 The permits tend to focus on and limit what the 16 regulatory authorities thought was important to limit, 17 and it did not set limits on other potential discharge 18 components. 19 Q. You understand, sir -- or do you understand - 20 what this lawsuit is about, and what the class of 21 representatives that I represent who are suing Monsanto 22 and Solutia is about? 23 A. I understand that there is a lawsuit in the 24 class and I would say in general what the issue is 25 about.
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1 Q. Describe for me, if you would, sir, what you
2 believe the lawsuit is about. 3 A. As I understand this lawsuit, it's a class of 4 property owners around a lake that are basically suing 5 the company for basically charges of diminished 6 property value. Basically that's what I understand it 7 to be . 8 Q. Do you understand it to be a lawsuit involving 9 a claim of damaged riparian rights to the property that 10 these people own? 11 A. I'm not that versed in the language in what 12 you've just said. 13 Q. Have you had any personal involvement in 14 working in this lawsuit, other than your conversations 15 with lawyers? 16 A. I don't know that I fully understand the 17 question, but I'm not -- I mean, this is the extent of 18 my involvement in the details of the legal proceeding. 19 Q. None of your employees, managers, agents have 20 discussed with you in official company meetings the 21 merits of this lawsuit, the potential ways to resolve 22 the lawsuit, or anything like that? 23 MR. PECK: I'm assuming with that question 24 you're excluding conversations he's had with his legal 25 counsel?
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1 MR. GRAMMAS: Yeah, that's a good assumption.
2 MR. PECK: To the extent that you're not, I 3 would object to the question. He's certainly not to - 4 MR. GRAMMAS: I don't want to - 5 MR. PECK: -- disclose communications with his 6 legal counsel. 7 BY MR. GRAMMAS: 8 Q. Any question I ask you today, Mr. Pierle, if 9 you interpret to mean to include conversations that 10 you've had with your attorneys, I don't want you to 11 answer the question to that extent. I'm not entitled 12 to that and I don't want to know that. But what I do 13 want to know is conversations you had with employees of 14 Monsanto or Solutia, your managers, your employees that 15 work under you, about the merits of this lawsuit and 16 ways to resolve it. 17 A. No. I'm really not involved in any of those 18 conversations, if it exists. I don't know that they 19 exist. 20 Q. Is it your position, then, or do you believe 21 that none of those conversations or those types of 22 conversations have occurred between Monsanto employees? 23 A. You know, I know this case is being handled by 24 the legal department and basically it's up to them to 25 determine what conversations do or don't happen.
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1 Q. What are your job responsibilities as -
2 basically you're the head of the entire environmental 3 department for Solutia, correct? 4 A. That's correct. 5 Q. And when I -- I will use "Solutia" and 6 "Monsanto" interchangeably in the lawsuit, especially 7 given the fact that your job duties really didn't 8 change much since you took this position. But for lack 9 of a better word, Mr. Pierle, the buck stops at your 10 desk with respect to environmental issues concerning 11 Monsanto and Solutia, right? 12 A. Yeah. I mean, I think that depends on what 13 you determine to be environmental issues. 14 Q. Well, PCBs being dumped into a river system, 15 does that fall under your direction? 16 A. Certainly matters with respect to the 17 regulatory side of that, the remediation side do. The 18 matters that pertain to the legal side do not. 19 Q. Right, I understand that. And what I want to 20 talk to you about is issues other than the legal 21 aspects of it. The lawyers will deal with that, but 22 what I want to know is, is what your responsibilities 23 are as the vice president of Solutia in dealing with 24 issues involving PCB contamination in river systems 25 and, in particular, in Anniston. What involvement have
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1 you had in considering these issues, if any?
2 A. At my level, I'm aware of the team working, 3 you know, at the plant site and with respect to the 4 various remediation projects, and am aware of and 5 involved in, where appropriate, the decisions 6 associated with those aspects around the Anniston 7 plant. 8 Q. Would that include cleaning up PCBs that 9 Monsanto put into the river system? 10 MR. PECK: Object to the form of the question. 11 THE WITNESS: It involves currently the work 12 that we're doing concerning both remediations that are 13 undertaken as well as investigations that are underway 14 today. 15 BY MR. GRAMMAS: 16 Q. Who set the policies for Solutia, and Monsanto 17 at the time, on what is going to be done, if anything, 18 to clean up PCBs that were discharged into Snow Creek, 19 Choccolocco Creek, and Lake Logan Martin? 20 MR. PECK: Object to the form of the question. 21 THE WITNESS: In general, policies have been 22 set, both at Monsanto and at Solutia, by policy 23 committees. They're not set by me, for example. 24 BY MR. GRAMMAS: 25 Q. Are you on the committee?
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1 A. In Monsanto, at a time, I was on an
2 environmental policy committee. In Solutia, those 3 decisions actually happen in a policy committee today, 4 but I'm not on that committee. 5 Q. Have you ever been on that committee? 6 A. Not in Solutia, no. 7 Q. Do you have the authority, sir, to order a 8 cleanup of the PCB contamination in Snow Creek,
9 Choccolocco Creek, and Lake Logan Martin?
10 A. I have the authority to make decisions with 11 respect to cleanup projects for the company to certain 12 levels. 13 Q. And what does that mean? 14 A. To the extent that there are decisions and to 15 the extent that the financial aspects of those are 16 quantified, I have authority to certain levels and at 17 certain levels I do not have authority. 18 Q. To what extent does your financial authority 19 go in ordering a cleanup of PCB contamination? 20 A. You've used the word "order." I don't think 21 I'm ordering, I believe the right terminology would be 22 in "approving" cleanup projects that come up through 23 the processes that are in place. I don't know if 24 that's responsive or not. 25 Q. Well, it's not, sir.
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1 The question was: How much money can you
2 direct -- or, how much cleanup can you direct and how 3 is it limited by money? 4 A. Yeah. The authority that I have is generally 5 at about $5 million per project, which in general is 6 significant to do most of the project and project work 7 that we have underway. 8 Q. How much money has Monsanto and/or Solutia 9 spent to clean up the PCBs around its own properties 10 and the neighboring properties out at the Anniston 11 plant to date? 12 A. I think in general the number we're using, on 13 a cumulative project basis, is somewhere around $30 14 million. 15 Q. And did anyone other than you -- did the 16 authority -- or, did the decision to do that cleanup 17 come from you, sir? 18 A. Again, the way the process works is that I 19 either have authority or it's been delegated authority 20 to commit to the work. 21 Q. All I want to know is: Did -- somebody at 22 Monsanto decided to spend $30 million to clean up its 23 own backyard. Who did that? 24 A. In some of those cases, on an aggregate basis, 25 those decisions were made inclusive of decisions at the
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1 board-of-director level. That's consistent with the
2 financial accounting requirements and practices. 3 Q. Who's on the board of directors today? 4 A. I don't have the full list of those people. 5 Q. Could you give me the list as complete as you 6 know it? 7 A. The internal members are Robert Potter and 8 John Hunter. 9 Q. John Hunter? 10 A. Right. 11 Q. Those are the only two? 12 A. Those are the only two Solutia employees that 13 are board of directors members. 14 Q. What about Monsanto employees? 15 A. Monsanto's not a member of the Solutia board. 16 It's a separate company. 17 Q. Who else is on the board besides Mr. Potter 18 and Mr. Hunter, that you're aware of? 19 A. I know that Bill Ruckleshouse (PHONETIC) is. 20 The balance of the board, I'm just not recalling their 21 names. 22 Q. Mr. Pierle, if you decided that a cleanup was 23 warranted in Anniston, Alabama, and the surrounding 24 areas of Snow Creek, Choccolocco Creek, and Lake Logan 25 Martin -- and when I say a "cleanup," I mean removing
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1 PCBs from the soils and sediments in the river
2 system -- do you have the authority to order that 3 cleanup to be done? 4 MR. PECK: Object to the form of the question. 5 THE WITNESS: With respect to projects -- and 6 I define "cleanup" different than that. It could be 7 inclusive of that, but it could be many other things. 8 To the extent that the financial cost is within my
9 authority or has been delegated by an action above me,
10 I would have the authority to commit to a project work. 11 BY MR. GRAMMAS: 12 Q. And your limit is a $5 million decision? 13 A. Unless larger levels have been approved and 14 authority delegated. 15 Q. If it costs a half a billion dollars to remove 16 the PCBs from Snow Creek, Choccolocco, and Lake Logan 17 Martin, would you have the authority to order a cleanup 18 of that magnitude? 19 A. No. 20 Q. Where would that go? Who would have to make 21 that decision, legal department? 22 MR. PECK: Object to the form of the question. 23 THE WITNESS: At that level, I mean, it's 24 difficult to comprehend, number one. So I assume 25 you're asking a speculative kind of question. Any
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1 authority that would require that level, if possible, 2 would clearly have to involve the board of directors, 3 the officers and the board of directors of the company. 4 BY MR. GRAMMAS: 5 Q. In 1966 when you began your employment, when 6 was the first time you heard about PCB-related issues? 7 A. It was probably in the '68-to-'69 period when 8 there was general literature information available on 9 an increased, I think, awareness in the country around 10 PCBs . 11 Q. Did Monsanto -- how many people -- how many 12 companies other than Monsanto manufactured PCBs here in 13 the United States? 14 A. I don't know. There were others, but I don't 15 know how many. 16 Q. You didn't understand who Monsanto's 17 competitors were during the time you were working with 18 them? 19 A. No . 20 Q. That wasn't something that concerned you? 21 A. No. 22 Q. What percentage of PCBs roughly, sir, did 23 Monsanto manufacture in the United States? 24 A. I don't know. 25 Q. Isn't it a true statement, sir, that Monsanto
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1 manufactured 98 percent of the PCBs in the entire
2 world? 3 A. I don't know. 4 Q. You've never heard those numbers? 5 A. No. 6 Q. Isn't it a true statement, sir, that Monsanto 7 was the overwhelming manufacturer of PCBs in the entire 8 world? 9 MR. PECK: Object to the form of the question. 10 THE WITNESS: I'm not aware of those facts or 11 what the market-share position was. I just don't know. 12 BY MR. GRAMMAS: 13 Q. Who manufactured PCB in the state of Alabama 14 other than Monsanto? 15 A. I don't know. 16 Q. You said you became aware of PCB-related 17 issues in the late '60s, 1968 time frame, I believe you 18 said. What was your knowledge of PCB-related issues at 19 that time? 20 A. In general there were questions raised about 21 the environmental significance of PCBs and there were 22 efforts at that time generally to understand PCBs and 23 their sources and presence in the environment. 24 Q. And where was this information or literature 25 coming from?
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1 A. Well, as I recall, some of that was just in 2 the general news, things of that nature. 3 Q. Was Monsanto studying the impacts of PCBs on 4 the environment at that time internally? 5 A. There was work inside Monsanto around that 6 time relative to understanding its PCB losses. I don't 7 know what else was going on. 8 Q. Most of the information was coming from 9 sources outside of Monsanto that you became aware of in 10 the 1968 time frame? 11 A. Yeah, at the front end of that. 12 Q. Do you believe, sir, that Solutia today has 13 the responsibility to fully research, before it ever 14 begins manufacturing, what environmental impact a 15 product may have before it begins making it? 16 A. I think that we do look at the product and its 17 properties and a fair amount of that is also now 18 regulated by government under rules, and we do that 19 work if we're in the business of looking at new 20 materials. 21 Q. Would Solutia manufacture a product that it 22 knew would have an adverse impact on -- let me ask you 23 this: As the chief environmental manager for Solutia 24 today, would you allow this company to manufacture a 25 product that you personally knew would have an adverse
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1 impact on the environment regardless of whether it was
2 regulated or not? 3 A. Under what use conditions? 4 Q. What do you mean? Under any use conditions. 5 A. If you manufactured a product with hazardous 6 properties but it was intended to be managed correctly 7 such that those did not cause damage, then I think 8 those kind of materials could be produced today.
9 Q. I understand that, and what I'm saying is:
10 Would you personally allow Solutia to manufacture a 11 product that you knew would have an adverse impact on 12 the environment regardless of how carefully you handled 13 that product even if it was not a regulated product? 14 MR. PECK: Object to the form of the question. 15 THE WITNESS: I think again in very specific 16 situations there can be products that are made today 17 that have hazardous properties that -- I mean, I can't 18 conceive of one not being true of regulatory approval, 19 which was part of your question. 20 BY MR. GRAMMAS: 21 Q. Right. And what I'm saying is: If you knew 22 something was going to have a bad impact on the 23 environment or people that used the product and you 24 were ahead of the curve on it and knew that in fact the 25 government didn't know about it, you wouldn't
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1 manufacture it anyway just because it wasn't regulated,
2 would you? 3 A. No. 4 Q. That's where I'm really coming from. And the 5 fact that a product is regulated or not really 6 shouldn't impact your decision on whether you're going 7 to manufacture it if you know personally that it's 8 going to have some type of adverse impact? 9 A. Under its intended consequences and use, 10 that's correct. 11 Q. Okay. Don't you think, sir, that Monsanto had 12 a responsibility during the decades that it was 13 manufacturing PCBs to fully understand the impact PCBs 14 had on the environment internally? 15 MR. PECK: Object to the form of the question. 16 THE WITNESS: I'm not sure that I understand 17 the question. 18 BY MR. GRAMMAS: 19 Q. Monsanto was the company manufacturing PCBs, 20 right? 21 A. One of the companies. 22 Q. And Monsanto manufactured PCBs in Anniston 23 from the '30s up to the '70s, right? 24 A. I believe that's correct. 25 Q. And over that 40-year period, don't you
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1 believe that Monsanto should have known everything
2 about that product and its adverse effects, if any, on 3 the environment - 4 MR. PECK: Object to the form of the question. 5 BY MR. GRAMMAS: 6 Q. -- as it was manufacturing it? 7 A. By the standards that were in existence during 8 that period of time. I mean, I think it would be 9 difficult to say by the standards that exist today or 10 the knowledge or whatever, that you would apply that 11 back to 1930. 12 Q. Well, the knowledge that we have today 13 about -- first of all, before I ask you that question, 14 you will agree with me that PCBs are a hazardous 15 product, won't you? 16 MR. PECK: Object to the form of the question. 17 THE WITNESS: PCBs do have hazardous 18 properties, that's correct. 19 BY MR. GRAMMAS: 20 Q. And it's not good to eat PCBs, is it? 21 A. I don't know that it's ever been shown to be a 22 true human health hazard. So the answer to your 23 question gets tied up into how much and when and what. 24 Q. Let me ask you a simple question. Would you 25 eat spoonfuls of PCBs every day?
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1 A. I mean, why would I? It's not part of a food
2 diet. So the answer to that is: Why would I want to 3 do that? 4 Q. It's not supposed to be in the food diet, is 5 it? 6 A. No, I'm sure -7 Q. You-all didn't manufacture PCBs to be eaten, 8 did you? 9 A. No. 10 Q. You don't want anybody eating PCBs, do you? 11 A. I wouldn't think that that would be something 12 somebody would want to sit down and intentionally do. 13 Q. It would actually be something that somebody 14 would want to avoid, wouldn't it? 15 A. Yeah, similarly you would avoid that on lots 16 of things. 17 Q. Like what? 18 A. Eating too much table salt, eating too much 19 sugar. I mean, lots of things that you would say, you 20 know, you just -- you don't want to do because they're 21 probably not healthy for you. 22 Q. And eating PCBs is one of them? 23 A. Again, the question there is: Does ingestion 24 of PCBs cause adverse health consequences? And I think 25 everything that we see says that has not been a proven
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1 conclusion.
2 Q. Okay. Now, you're the head man over the 3 environmental safety issues for Solutia. 4 A. That's correct. 5 Q. And I assume that you have read articles 6 regarding adverse health effects PCBs have on human 7 beings. 8 A. I have read a fair amount of information that 9 discusses that topic. 10 Q. And you, as the head of the environmental 11 affairs at Solutia and once held that same position at 12 Monsanto, are testifying that you're unaware of a 13 single scientist who has concluded that ingesting PCBs 14 poses a health hazard to human beings? 15 MR. PECK: Object to the form of the question. 16 Mischaracterizes his prior testimony. 17 THE WITNESS: Yeah, I didn't say that. 18 BY MR. GRAMMAS: 19 Q. I thought you said that there's nothing really 20 proven that PCBs cause adverse health effects in human 21 beings. 22 A. That wasn't the question you asked me. 23 Q. Did you not testify to that, Mr. Pierle; did I 24 misunderstand you? 25 A. I think what I said was that our general
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1 conclusion, looking at all the information about PCB
2 studies, health studies, and all that, is that it does 3 not indicate that PCBs have been shown to be a human 4 health -- or, an adverse human health material. 5 Q. Are you aware of a single scientific study 6 that disputes what you just told me? 7 A. I can't tell you specifically studies. There 8 are many of them at different doses that look at dose
9 response and that, but in general, the conclusion we
10 make out of the body of studies is that that is not - 11 that is not an appropriate conclusion. 12 Q. Okay. And what I'm hearing you saying, Mr. 13 Pierle, is that you're looking at a group of studies 14 and you're reading all of them that you're aware of and 15 that you have read, and then after you've read all of 16 these studies, you're making a conclusion on your own 17 based on the work of other people as to whether or not 18 PCBs cause or may cause adverse human health effects, 19 right? 20 A. Yes. 21 Q. Now, some of those find that it doesn't, I 22 assume, is what you're testifying to, correct? 23 A. I haven't looked at every individual study. 24 I'm saying that when I talk with experts in my 25 department and look at that, that is the general
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1 conclusion that we come to.
2 Q. Have you personally ever read a single 3 scientific study that disagrees with your conclusion 4 that you've testified to today? 5 A. My conclusion is based upon the weight of 6 evidence of all of the information, and there are 7 varying studies in there. 8 Q. So the answer - 9 A. So the proper way to look at it is to look at 10 all the information, not to look at individual studies, 11 but to look at all the information and derive 12 conclusions from the body and the weight of evidence of 13 all the studies. 14 Q. You've never seen a study that says that PCB 15 ingestion causes adverse health effects or may cause 16 adverse human health effects; is that your testimony, 17 yes or no? 18 A. No. 19 Q. So, then, can I understand that you have seen 20 scientific studies that suggest that ingestion of PCBs 21 causes or may cause adverse human health effects? 22 A. Yes, I have seen the studies. 23 Q. Okay. And can you identify who these people 24 were that conducted these studies? 25 A. I don't recall.
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1 Q. Were they Monsanto employees?
2 A. I don't believe so. 3 Q. Do you know of a single study conducted by 4 anyone within Monsanto or Solutia that has concluded 5 that the products that this company manufactured for 30 6 years, PCBs, cause or may cause adverse human health 7 effects if ingested? 8 A. I don't know of any. 9 Q. Are you aware of any studies that Monsanto has 10 conducted that show the opposite conclusion; in other 11 words, that ingestion or exposure to PCBs does not 12 cause adverse human health effects? 13 A. Again, I'm not familiar with each and every 14 study that we have conducted or others have conducted. 15 That's just not a level of detail, I think I said, that 16 I would get down to. I rely on the experts in the 17 organization that have worked for both companies to 18 provide general conclusions and recommendations in 19 those areas. 20 Q. What did you do for the Department of Commerce 21 in 1974 and 1975? 22 A. I was basically on loan in the Department - 23 or, the Commerce Department, in a small group there 24 that was the Office of Environmental Affairs, and our 25 primary role was to participate on behalf of the
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1 department in a governmental process that was called
2 Quality and Life Review on Governmental Regulations. 3 Q. Did it have anything to do with regulating 4 PCBs? 5 A. None. Did the process have any -- I don't 6 know whether the process did or not during my period of 7 time. I specifically stayed away from any regulatory 8 matters that were pertaining to the chemical industry. 9 Q. Why is that? 10 A. I think as basically just a prudent step that 11 says that --my background was in that industry, there 12 should be no question about being involved in any 13 regulations that would pertain to that industry. There 14 were plenty of other folks in the department that could 15 look at those things, and I specifically focused on 16 things outside that industry. 17 Q. Who paid for your services at that time? 18 A. I was an employee of the Department of 19 Commerce. 20 Q. Did you give them any special types of breaks 21 or anything as far as how much money you would receive 22 during that period of time? 23 A. No. 24 Q. Why is it that they selected you to do this, 25 sir?
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1 A. In the Department --at Commerce, in that
2 group, they had a practice of rotating on an -- roughly 3 an annual basis, somebody out of industry and in prior 4 years it had been other companies and I'm not really 5 sure how my name got into the nomination process. And 6 so I was nominated and accepted and spent a year there 7 and then returned to Monsanto. 8 Q. And it was always known that it was going to 9 be a one-year position and that you were going to 10 return to Monsanto when the position was completed? 11 A. No. It was -- you asked two questions there. 12 One, it was known that it was going to be a one-year 13 assignment, but I was under no obligation to return to 14 Monsanto. I had basically stopped my employment with 15 Monsanto Company prior to that. 16 Q. This bio, Exhibit 1, says in 1974 to 1975 you 17 were "on leave" to work for the Department of Commerce. 18 That suggests to me that Monsanto knew that you were 19 going to do this and encouraged you to do it and 20 allowed you to do it and wanted you to come back when 21 you were through. Am I reading that wrong? 22 A. Basically they encouraged it. They did 23 basically allow it, but the point is that I had no 24 contractual commitment to come back. They had no 25 commitment to me to a specific position, and I had no
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1 commitment to come back. I think the hope was that, 2 from a personal standpoint, I'd be able to return in 3 another responsible position. 4 Q. What benefits did Monsanto receive, if any, 5 from you working for the Department of Commerce in the 6 Office of Environmental Affairs during that year? 7 A. None. 8 Q. There wasn't any political advantage gained? 9 A. No. I mean, I was a Grade 14GS person. I 10 mean, it was a learning position. It wasn't a position 11 of influence or consequence in the department. 12 Q. Do you believe that the single biggest 13 challenge today that Monsanto and Solutia now has is 14 PCB-remediation issues, as far as environmental cleanup 15 issues? 16 A. I mean, it's an important issue to us. I 17 don't know whether it's the single biggest issue and I 18 can't speak for Monsanto. Their issues today are much 19 different. 20 Q. And when I say "Monsanto," I don't mean 21 Monsanto as of September 1997, I mean Monsanto prior to 22 the spinoff of Solutia and the responsibilities that 23 you held with Monsanto. Do you understand what I'm 24 saying? 25 A. Not really.
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1 MR. PECK: Your question, Pete, was asking for
2 a current -- you said "today." Today Monsanto and 3 Solutia are two separate companies. I think that he's 4 got to make that distinct. 5 MR. GRAMMAS: That's fair. 6 BY MR. GRAMMAS: 7 Q. If, sir, you don't believe that PCBs cause 8 human adverse human health effects, why is it that 9 you're concerned about remediation of them in the first 10 place? 11 A. I think we are in a process that began, you 12 know, a few years back at the plant site with respect 13 to PCBs, whether or not they exist at levels that would 14 cause adverse harm to the environment or to people, and 15 I think that our posture through this process is to 16 make sure that we understand that question and whether 17 or not there is a basis then for action. So we're in 18 it to understand and to find out and to discover 19 whether there are issues or situations that need 20 attention. 21 Q. Okay. Monsanto knew in the '50s that PCBs can 22 cause adverse human health effects, didn't it? 23 A. I don't know that for a fact. 24 Q. You've never seen literature from Monsanto 25 employees that said. We know PCBs are toxic to humans,
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1 in the '50s? 2 A. Again, I have not gone back and looked at all 3 those documents. I wasn't involved in that. I mean, I 4 wasn't even employed at that time. 5 Q. Well, I wasn't even born at that time, sir, 6 but I've read a document produced by your company that 7 said that they knew in the late '50s that -- this is a 8 document that I've seen, I'm sure there are others, but 9 one of the documents that I've seen said that Monsanto 10 knew in the late '50s that PCBs cause adverse human 11 health effects. 12 MR. PECK: Object to the form of the question. 13 I don't think that's an accurate characterization of 14 the document. If you want to ask him about the 15 document, show him the document. 16 BY MR. GRAMMAS: 17 Q. It seems to me, sir, as the head man over the 18 department of environmental affairs at Solutia, you 19 would at least be aware of such a document. 20 MR. PECK: Object to the form of the question. 21 It mischaracterizes the document. 22 BY MR. GRAMMAS: 23 Q. Is it your testimony that you've never seen 24 any documents dated back in the late '50s that 25 discussed human health effects on PCBs?
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1 A. You know, I don't recall what I have or
2 haven't seen. 3 Q. All right. Well, at some point you will admit 4 that you became aware -- "you" being Monsanto, now 5 Solutia, and you personally -- became aware that PCBs 6 do in fact cause adverse human health effects at some 7 level of exposure? 8 A. I think most of the discussion of my
9 recollection around PCBs is around environmental
10 consequences, not human health consequences. 11 Q. When did you first become aware that PCBs harm 12 the environment? 13 A. Again, I think the data that I referred to in 14 the late '60s was around whether or not PCBs are 15 causing or alleged to be causing issues with respect to 16 environmental and critters within the department. 17 Q. How do PCBs hurt the environment? 18 A. I think the concerns are whether or not they 19 can -- at that time, interfered with certain processes 20 around birds and eggs that caused soft shells, and the 21 question was: Are PCBs a causative agent in what was 22 being observed at that time? 23 Q. Any other factors that show PCBs hurt the 24 environment? And don't limit your knowledge to that 25 time. Tell me all the ways you're aware of that PCBs
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1 harm the environment.
2 MR. PECK: Object to the form of the question. 3 THE WITNESS: Again, you know, I don't recall 4 the specific studies and works. I think what we're 5 looking at is whether or not, because of information 6 about PCBs, which I've described, we're to be sensitive 7 to whether or not they are in the environment and
8 causing any concern, and that's why we're doing the
9 studies and the work that we're doing today, to see 10 whether or not remediation is necessary and 11 appropriate. 12 BY MR. GRAMMAS: 13 Q. You're talking about remediation in Anniston? 14 A. That's correct. 15 Q. Here's where I'm getting at, and it's probably 16 obvious: Monsanto's known since the '50s and '60s that 17 PCBs cause harm, to both the environment and to 18 individuals, at certain levels. I realize Monsanto 19 debates what levels cause harm and all that, I 20 understand that. But at certain levels, everyone in 21 the world will agree that PCBs cause harm to the 22 environment and human beings, and Monsanto's known it 23 since the '50s and '60s. Here it is 1998. We're 24 almost at the year 2000 and it's your testimony that 25 Monsanto, and now Solutia, is still studying the issue
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1 as to whether it causes harm to the environment or not
2 to determine whether you're going to remediate it or 3 not; is that your testimony, sir? 4 MR. PECK: Object to the form of the question. 5 It completely mischaracterizes his testimony, misstates 6 numerous facts, and is completely without foundation. 7 If you can answer that question, you can try. 8 THE WITNESS: I can't answer it. 9 BY MR. GRAMMAS: 10 Q. Why can't you? 11 A. You asked -- you've stated several things 12 which I don't believe are true, and you've stated them 13 three or four times and I think we've covered that. So 14 how do I answer a question that has within it 15 statements that we believe are not true? 16 Q. What statements in there do you believe are 17 not true? 18 A. Well, you've dealt with "known to cause" and 19 "several studies" about the human health consequences 20 of that. So I don't -- you went on for a long period 21 of time, and you've got me, I guess, at the minimum, 22 confused. 23 Q. Okay. Well, let me break it down. Since the 24 '60s, Monsanto became aware of knowledge that PCBs harm 25 the environment, true or false?
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1 A. I would add the word "could" harm the
2 environment, and then I would agree with you. 3 Q. You're not convinced, as the head 4 environmental person at Solutia, that PCBs do in fact 5 harm the environment; is that what I'm hearing you say? 6 A. I think what I'm saying is that the work that 7 we're underway with is to understand whether or not 8 PCBs exist, whether they are at levels that could harm 9 the environment, and whether or not something needs to 10 be done about those. And that's the process that is a 11 very common process that's used throughout the United 12 States to deal with remediation issues, and that's the 13 process we're in. 14 Q. When did that process in Anniston begin? 15 A. My more recent understanding is that it was 16 sometime in the '90s when there was some data around 17 the storm water permit that raised a question as to 18 whether or not PCBs were leaving the site,- and that 19 information, which we acted on diligently and pursued, 20 has led to a continuation of studies and understanding 21 in the area and project-related work. 22 Q. Monsanto did not begin this process of 23 studying whether or not the PCBs are harming the 24 environment until the 1990s in Anniston? 25 A. I don't know when they may have started or if
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1 they had done anything before that. What I'm saying is
2 that my recollection of what started this level of 3 study began at about that time. 4 Q. And Monsanto at that very plant manufactured 5 PCBs from the '30s through the '70s, true? 6 A. I believe that's true. 7 Q. And during that entire period of time, 8 Monsanto engaged in a process it called "sewering," did 9 it not? 10 MR. PECK: Object to the form of the question. 11 BY MR. GRAMMAS: 12 Q. Have you ever heard of that? 13 A. No. 14 Q. You've never heard of the word "sewering"? 15 A. I know what sewering is. 16 Q. What does "sewering" mean? 17 A. It's a discharging of materials into a sewer. 18 That would be my common definition of that. 19 Q. You're not aware that it was common practice 20 for employees at the Anniston plant in Monsanto to 21 sewer PCBs out of its plant into Snow Creek and 22 Choccolocco Creek during that entire period of time of 23 manufacture? 24 MR. PECK: Object to the form of the question. 25 Lack of foundation.
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1 THE WITNESS: It's my understanding that there
2 was a discharge from that plant site that went through 3 a neutralization treatment basin and subsequently was 4 discharged. 5 BY MR. GRAMMAS: 6 Q. Into Snow Creek/Choccolocco Creek? 7 A. I believe that's correct. 8 Q. Now, over that 40-year period while Monsanto 9 is dumping all the PCBs into this river system, why 10 didn't it study the effects of PCBs during that time? 11 Why did it wait until the '90s to engage in this 12 process you're now talking about to determine what 13 impacts if any PCBs have on the environment and the 14 folks that live down there? 15 MR. PECK: Object to the form of the question. 16 THE WITNESS: I don't know what they did, you 17 know, relative to plant operations and what was done at 18 that point in time. It was certainly not a common 19 practice. I mean, you're looking at a set of processes 20 that exist today that did not exist years ago, so 21 you're sort of applying a set of understandings to 22 conditions 40 years ago that simply didn't exist. 23 BY MR. GRAMMAS: 24 Q. That brings up an interesting point. Does 25 Monsanto, and now Solutia, take the position that it
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1 was perfectly proper for them to dump PCBs into the
2 river system during the '30s, '40s, '50s, '60s, and
3 early '70s?
4 MR. PECK: Object to the form of the question.
5 BY MR. GRAMMAS:
6 Q. "Because everybody was doing it we could do 7 it. " 8 MR. PECK: Object to the form of the question.
9 Assumes facts not in evidence.
10 THE WITNESS: I don't know how to answer that. 11 BY MR. GRAMMAS: 12 Q. Truthfully. 13 A. Of course. 14 Q. You were dumping them. Not you personally, 15 but your company was dumping them into the rivers. 16 A. There were discharges and systems in place, 17 and what was common practice at that point in time was 18 that many effluents of treatment from cities, from 19 homes, and from industry plants were basically 20 discharged into rivers and streams. That was a very 21 common practice. 22 Q. Including Monsanto, in Anniston, PCBs, 23 correct ? 24 MR. PECK: Object to the form of the question. 25 Asked and answered.
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1 MR. GRAMMAS: It's been asked, but it hasn't
2 been answered yet. 3 MR. PECK: He explained to you how the system 4 worked, Pete. You didn't like the answer, so you 5 changed the facts of the question. 6 BY MR. GRAMMAS: 7 Q. You can answer the question, Mr. Pierle. 8 A. I think what I told you was I don't know what
9 the facts were in the '40s, and that's what you're
10 asking me now to discuss. 11 Q. Okay. You're the head honcho for remediation 12 on PCB-related issues as we sit here today, right? 13 A. That's within my department. 14 Q. And you don't report to anybody, really, other 15 than the board of directors. 16 A. That's not true. I didn't say that. 17 Q. With respect to remediation. 18 A. Correct. I have a supervisor. 19 Q. Who's your supervisor? 20 A. My current supervisor is John Ferguson. 21 Q. And what position does he hold with Solutia? 22 A. I'm not sure of his exact title, but he is the 23 head of the shared service organization, of which I am 24 a member. 25 Q. What is that? I've never heard of that.
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1 A. It basically -- the environmental safety and
2 health department provides services to the enterprise 3 and other functions that provide service to the 4 enterprise and we report to John, who is the supervisor 5 of that shared service group. 6 Q. What enterprise? 7 A. Solutia. 8 Q. Is that shared service with Monsanto? 9 A. No. 10 Q. Sort of like a blend of Monsanto/Solutia 11 employees? 12 A. This is Solutia. 13 Q. Okay. Now, don't you believe, sir, as the 14 senior employee of environmental affairs, charged at 15 least in part with the responsibility of deciding 16 whether a remediation should take place in Anniston 17 regarding PCB exposure and contamination, that you 18 should have an understanding of the amount of PCBs that 19 were put into that river system by Monsanto and now 20 Solutia? 21 MR. PECK: Object to the form of the question. 22 THE WITNESS: I think what we're trying to 23 understand with the work that we're doing now is what 24 is the situation today, ' the factual situation with 25 respect to the presence of PCBs, and that's what we've
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1 been working diligently on and are continuing to work
2 on. 3 BY MR. GRAMMAS: 4 Q. And that's the work you started in the 1990s? 5 A. That's correct.
6 Q. And Monsanto knew about --as you put it -
7 the potential adverse impacts PCBs would have on the 8 environment as early as the late 1960s. 9 A. I think I said what, the late '60s? 10 Q. 1968 is really what you said. 11 A. Okay. 12 Q. So Monsanto knew in 1968 that PCBs could cause 13 harm to the environment, right? 14 A. Could. 15 Q. Monsanto knew from 1968 to the early 1990s, 16 before this diligent study began that you're talking 17 about, that it put PCBs into Snow Creek, Choccolocco 18 Creek, and Lake Logan Martin, right? 19 MR. PECK: Object to the form of the question. 20 It mischaracterizes his testimony. 21 MR. GRAMMAS: That's not a 22 mischaracterization, Adam. I'm asking him this 23 question. How can I mischaracterize something he 24 hasn't answered? 25 MR. PECK: Well, you have asked him, he has
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1 answered, and now you're mischaracterizing it.
2 BY MR. GRAMMAS: 3 Q. Monsanto knows, sitting here today -- Solutia 4 knows, sitting here today, that Monsanto put PCBs into 5 Snow Creek, Choccolocco Creek, and Lake Logan Martin, 6 true or false? 7 A. That's not true. 8 Q. You don't believe that Monsanto put PCBs into 9 Snow Creek, Choccolocco Creek, and Lake Logan Martin? 10 A. I believe what I said to you is that we are - 11 part of this work and investigation is trying to find 12 out answers to those questions. 13 Q. One of the questions you-all are actually 14 studying -- and if I'm understanding your testimony 15 correctly, Mr. Pierle, you were truthfully telling me 16 under oath that you're going to study whether or not 17 y'all are a responsible party for putting the PCBs in 18 that system?
19 A. I think that is one of the most important
20 questions that we need to factually understand. 21 Q. Is there any doubt in your mind, sitting here 22 today, under oath, testifying, that Monsanto is a party 23 that put PCBs into Snow Creek, Choccolocco Creek, and 24 Lake Logan Martin? 25 A. Listen, we wouldn't be there if we weren't
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1 trying to understand factually that question and 2 whether we are or others are or aren't. That's what 3 we're trying to find out. 4 Q. That's not what I asked you, Mr. Pierle. I 5 asked you: Sitting here today, as the head 6 environmental manager for Solutia, is there any doubt 7 in your mind that Monsanto is a responsible party for 8 putting PCBs into Snow Creek, Choccolocco Creek, and 9 Lake Logan Martin? 10 A. And I think I answered that question. 11 Q. I didn't hear the answer if you did. 12 A. Then I'll repeat it, I guess, is that we're 13 down there trying to find out the answer to that 14 question. I don't presume anything with respect to 15 these situations and remediations. The facts need to 16 be found out and they will speak for themselves at that 17 time . 18 Q. Don't you think these studies should have been 19 conducted back in the '60s when you-all first became 20 aware that PCBs you were making may have an adverse 21 impact on the environment? 22 MR. PECK: Object to the form of the question. 23 Asked and answered. 24 THE WITNESS: I don't know that the questions 25 and the reasons why we're pursuing things today,
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1 whether they would have existed have been known to
2 prompt those questions at that time. 3 BY MR. GRAMMAS: 4 Q. In fact, what prompted this diligent research 5 you're talking about in the 1990s is the fact that 6 you're being sued over PCB contamination in the river 7 system; isn't that true? 8 A. No.
9 Q. And if you weren't being sued, you wouldn't be
10 studying it sitting here today, would you? 11 A. No, we would. 12 Q. Well, you weren't sued in 1968 through the 13 early 1990s, were you? 14 A. We did begin our work before there were any 15 suits. The suits were filed as a result of the 16 information which began and became available as a 17 result of the work that we're doing. So I think the 18 sequence is fairly clear as to where the suits -- and 19 when they started in this time line. 20 MR. PECK: Can we take a break? 21 MR. GRAMMAS: Sure. 22 (A SHORT BREAK WAS HELD.) 23 BY MR. GRAMMAS: 24 Q. Mr. Pierle, how in the world can Solutia 25 undertake a legitimate study of this problem, as you've
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1 been testifying, without understanding the history of
2 PCB exposure or discharging from the Anniston plant 3 into the river system? 4 A. I think part of what, you know, we're trying 5 to understand in that study is a variety of things that 6 would include what you've described as well as issues 7 around the presence, as well as the hydrogeology of the 8 systems and the whole complexity of that. So, you 9 know, my sense is that again is part of the work that 10 is ongoing down there at this point. 11 Q. Why 1990? And can you give me a more specific 12 date as to when this project began? 13 A. I can't. I know it started with -- or at 14 least a part of the issue was around the storm water 15 permit application where we discovered some 16 information. There were also some discussions on the 17 West Side Landfill or something, but that's my 18 recollection of what -- of where this sequence of 19 events began. 20 Q. 1993, Alabama Power and Monsanto had an issue 21 relating to some property that was swapped back in the 22 '60s; is that your recollection? 23 A. That's correct. 24 Q. Is that what started all this? 25 A. Well, that was part of it. As I say, there
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1 were sort of events that were happening around the same
2 time . 3 Q. These studies didn't begin before 1993, then, 4 is what I'm hearing you say? 5 A. I think what I said is that I don't recall 6 exactly when they did begin. 7 Q. I understand the exact date you're not going 8 to be able to recall, but they didn't begin before that 9 1993 Alabama Power land issue, did they? 10 A. I don't know. 11 Q. All right. Now, what in the world is Monsanto 12 going to do to determine the number of pounds of PCBs 13 it dumped into Snow Creek and Choccolocco Creek during 14 the history of its manufacturing processes? 15 A. I think what we've been focusing on there is 16 what's present and what needs to be determined. That's 17 what we got into up around the plant sites and in the 18 front end of Snow Creek. So I think we're trying to 19 deal with what is the current situation and facts and 20 help us understand whether or not there is a basis 21 for -- and a requirement for remediation and the extent 22 that Solutia should be involved. 23 Q. Does Monsanto accept responsibility for the 24 PCBs contained in the upper portion of Snow Creek as 25 you just described -- or, found rather?
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1 A. I mean, what we've been doing is working and
2 trying to -- as we determine that -- and we're doing 3 some projects which we're basically trying to correct 4 and take responsibility for and do appropriate 5 remediation. 6 Q. In the late 1980s the Alabama attorney general 7 noticed a PCB problem at the Monsanto site. Are you 8 aware of that? 9 A. I have some vague recollection that there was 10 an issue back sometime in the '80s that resulted in 11 some cleanup and removal of materials. 12 Q. And Monsanto spent several hundred thousand 13 dollars cleaning up or removing sediment from Snow 14 Creek at that time, didn't it? 15 A. I don't recall what the cost was. 16 Q. But you do recall that Monsanto removed 17 sediment from Snow Creek that contained PCBs? 18 A. Yes. 19 Q. Did Monsanto take responsibility for putting 20 the PCBs there? 21 A. I think, in simple terms, by the fact that we 22 went ahead and did that, we probably didn't debate the 23 accountability. We said it ought to be done. There's 24 at least a likelihood that they came from the site, so 25 we ought to get on and deal with that situation.
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1 Q. You're the head guy here over environmental
2 affairs and the head guy over remediation, Mr. Pierle,
3 and all the other witnesses we've talked to have
4 pointed up the chain to you, which is how we got to 5 your deposition. Is there any doubt in your mind that 6 the PCBs in that part of Snow Creek that Monsanto went 7 in and removed came from Monsanto's plant process, any 8 doubt whatsoever? 9 A. I mean, there's a set of facts that I'm just 10 simply not aware of at that point in time. There was 11 enough justification obviously for the folks who were 12 in charge at the time to go do something and be 13 involved with that. I don't know what the whole set of 14 facts were about that. 15 Q. I'm going to show you what's been marked as 16 Plaintiff's Exhibit 2 and ask if you recognize that to 17 be a Monsanto news release dated approximately 1970? 18 A. That's what it's entitled and dated. 19 Q. And does that look to be the official company 20 Monsanto letterhead and that type stuff? 21 A. It looks like it is. 22 Q. Okay. Read out loud, please, for the jury the 23 first sentence on the news bulletin. 24 A. "Monsanto Company, sole U.S. producer of an 25 industrial chemical called polychlorinated biphenyl
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1 (PCB), today said recent political charges and
2 sensational headlines about the chemical causing a 3 major ecological crisis completely ignore voluntary 4 actions the company has taken to restrict use of the 5 material." 6 Q. According to that news release that Monsanto 7 put out, sir, isn't it true that Monsanto was the only 8 producer in the entire United States of PCBs? 9 A. That's what this says. 10 Q. And you don't have any reason to dispute that, 11 do you? 12 A. No. 13 Q. Tell me, have you ever had any course studies 14 particularly designed to educate you on PCB-related 15 issues ? 16 A. No. 17 Q. Do you feel like, as the head environmental - 18 manager of remediation, that's something that you 19 should be extremely familiar with? 20 A. I think those are the -- the details of that 21 are what I have a very competent staff and experts in 22 the organization to understand, and I rely on them 23 to -- for that detailed knowledge and understanding. 24 Q. Do you consider PCBs to be a hazardous waste? 25 A. There are some regulatory definitions of that
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1 and I don't know whether PCBs are, quote, "a hazardous
2 waste" by regulation or not. 3 Q. Is it because it's not important enough for 4 you, sir, to determine whether they are a hazardous 5 waste or not? 6 A. No. 7 Q. You don't believe that as the head man over a the environmental affairs and, in particular, 9 remediation projects for PCBs, you don't need to know 10 whether it's a hazardous waste or not?
11 A. I think people inside my organization that 12 work for me know the answer to that question very
13 specifically, and I rely and must rely on their 14 knowledge and judgment. 15 Q. I mean you personally, sir. You're the man 16 who makes decisions on which direction this company 17 will take as far as environmental policy, right? 18 A. Would you repeat the question. 19 Q. Yes, sir. You're the man who makes decisions 20 with respect to which direction Solutia will take with 21 respect to environmental policy? 22 A. In part, that's correct. 23 Q. And one of the decisions you made while you 24 were the vice president of environmental affairs at 25 Monsanto, and continue to make while you're the vice
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1 president at Solutia, is to rectify the mistakes of the
2 past that this company has made, correct? 3 A. I do not categorize these as mistakes. 4 Q. You don't believe it was a mistake for 5 Monsanto, for almost a 40-year period, to dump 6 thousands of pounds of PCBs into Snow Creek, 7 Choccolocco Creek, and now Lake Logan Martin? 8 MR. PECK: Object to the form of the question. 9 It assumes facts not in evidence. 10 BY MR. GRAMMAS: 11 Q. You don't believe that was a mistake, even 12 looking back with perfect 20/20 hindsight, Mr. Pierle? 13 A. You can't look back and ask that question 14 legitimately. That's the fallacy of your question. 15 Q. No, that is the beauty of the question because 16 we can. That's the purpose of - 17 MR. PECK: Pete, you can ask him questions. 18 We're not here to have your jury speeches read into the 19 record. Ask him questions and he will answer them. , 20 BY MR. GRAMMAS: 21 Q. Mr. Pierle, did you or did you not take the 22 position that your company is charged with the 23 responsibility of rectifying the mistakes of the past? 24 A. We're responsible for understanding whether or 25 not we have obligations today that may deal with issues
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1 of the past and we are about fulfilling those
2 responsible obligations. 3 Q. I'm going to ask you a very simple 4 straightforward question and it calls for a yes-or-no 5 answer. If you want to explain it after that, I 6 encourage you to do so. You're the environmental 7 manager for Solutia. Sitting here under oath, sir, is 8 it your testimony that Solutia should correct the 9 mistakes that it has made in the past, yes or no? 10 A. I have commented already on your definition of 11 the word "mistakes." I think that, you know, 12 throughout the time that I've worked at Monsanto, we 13 have been very responsible about our actions with 14 respect to a lot of things, including the environment 15 and the health of our workers and communities, and I 16 think that we have acted always in that fashion. 17 Q. Well, Mr. Pierle, if Monsanto -- and if I 18 understand what you're saying is, during the period of 19 40 years when Monsanto was discharging these PCBs into 20 the environment, it was not aware of a problem in doing 21 so; is that what you're saying? 22 A. I'm saying that, again, my understanding is 23 that we have acted as the responsible person given the 24 norms and standards and expectations that existed at 25 the -- at that point in time.
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1 Q. Right. So what you're saying is that in the 2 '30s, '40s, '50s, '60s, and '70s, when there were no
3 applicable federal regulations, when there were no 4 state regulations confining or describing how Monsanto 5 should discharge PCBs, it was acceptable at that time 6 during those decades for Monsanto to discharge PCBs 7 into the environment as waste? 8 A. Yes, and based upon, you know, the knowledge 9 of information that was available at that time. 10 Q. At that time. So if we later learn that that 11 was not a good practice, in hindsight can't we look at 12 it and say that was a mistake to do that? It may not 13 have been a mistake in your mind at the time, but can't 14 we look at it in hindsight, sitting here today, and say 15 that was wrong, that was a mistake? 16 A. No, I don't think that you can -- I don't 17 think you can say that. 18 Q. Okay. So the only way that Monsanto will 19 rectify mistakes of the past is if the mistakes in the 20 past were intentionally done and at the time were known 21 to be mistakes? 22 MR. PECK: Object to the form of the question. 23 Mischaracterizes his testimony. 24 THE WITNESS: I think I've been fairly clear, 25 and what I'm saying is that as we learn more about what
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1 happened in the past and we apply today's standards and 2 expectations, then we are about taking care of those
3 issues. I do not categorize those as mistakes. 4 BY MR. GRAMMAS: 5 Q. So when Mr. -- who's Mr. Mahoney, Richard J. 6 Mahoney? 7 A. He's a former chairman of Monsanto Company. 8 Q. Where is he today? 9 A. I have no idea. 10 Q. Did he get fired? 11 A. He retired. 12 Q. Is he in St. Louis? 13 A. I have no idea. 14 Q. Do you know the man personally? 15 A. I certainly have met him and know him, but 16 we're not personal -- close personal friends or 17 contacts. 18 Q. Do you respect the man as far as a 19 professional? 20 A. Yes. 21 Q. Did you follow the commitments that he made 22 for the Monsanto Company while you were employed by 23 Monsanto? 24 A. I believe I did. 25 Q. Was he your boss?
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1 A. No. 2 Q. He wasn't your boss?
3 A. Not my immediate boss. He was everybody's 4 boss . 5 Q. That's right, including yours, because he was 6 the chairman of the board at Monsanto. 7 A. That's correct. 8 Q. And no one was higher, as far as an officer's 9 position, than Mr. Mahoney on January 30, 1990? 10 A. He reported to the board of directors. 11 Everybody always has a boss. 12 Q. But no single individual was a higher person 13 than Mr. Mahoney. 14 A. He was the chairman and CEO of the company, 15 that's correct. 16 Q. And if he said in an official statement that 17 Monsanto must rectify the mistakes of the past, you're 18 testifying to this jury that that does not mean 19 cleaning up PCBs that it discharged into a river system 20 over 30 years, because you don't believe that was a 21 mistake? 22 A. That's not what I'm saying. 23 Q. Well, that's what I'm trying to get at, sir. 24 Do you believe, yes or no -- and I think you've already 25 answered it -- that it was not -- strike that. Too
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1 many negatives. 2 Do you believe, yes or no, that it was a
3 mistake for Monsanto to discharge PCBs into Snow Creek, 4 Choccolocco Creek, and now Lake Logan Martin over a 5 40-year period? 6 MR. PECK: Object to the form of the question. 7 THE WITNESS: Yeah. Again, I think what I've 8 said is, you know, looking back, had we wished we 9 hadn't done certain things? By today's standards, 10 that's probably a right thing to do and to say and 11 that's what we're about, trying to resolve today and 12 over the last several years. 13 BY MR. GRAMMAS: 14 Q. Okay. I'll ask the question again because it 15 was obviously confusing. Do you believe, sir, that 16 Monsanto discharging PCBs out of its plant in Anniston 17 into Snow Creek, Choccolocco Creek during the 1930s, 18 '40s, '50s, '60s, '70s was a mistake? 19 MR. PECK: Object to the form of the question. 20 THE WITNESS: By today's standards? 21 BY MR. GRAMMAS: 22 Q. Yeah. 23 A. I'm troubling with -24 Q. By today's standards. 25 A. I'm just going to answer it that basically it
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was something that I wished wouldn't have happened. That doesn't mean that -- in my mind, that that is a
mistake.
Q. Okay. Again, sir, my question has not been
answered.
MR. PECK: You have asked it twice. He's
answered it twice.
MR. GRAMMAS:
I have asked it twice.
MR. PECK: You don't like it.
I'll let you
ask it one more time.
MR. GRAMMAS: I'll ask it as many times as it
takes to get an answer.
MR. PECK: That ain't going to happen.
MR. GRAMMAS: Well, it's going to happen.
MR. PECK:
It's not going to happen.
BY MR. GRAMMAS:
Q. Do you personally believe, as the senior
environmental manager for Solutia, that Monsanto's
discharging of PCBs into Snow Creek and Choccolocco
Creek during the 1930s through the '70s was a mistake,
yes or no? And if you want to explain it, you can, but
the question is simple: Was it a mistake?
MR. PECK: You can answer the question however
you want. You don't have to accept Pete's instruction
as to how to answer the question.
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THE WITNESS: Again, I think I've tried to be
pretty clear on this, that had I wished it didn't
occur? Yes. Are we about taking care of it? Yes.
In
my mind, you're using the word "mistake" and that, to
me, is not a mistake.
BY MR. GRAMMAS:
Q. So when Mr. Mahoney stood up at a meeting of
the Corporate Conservation Council of the National
Wildlife Federation, of which you were on the board of
directors, on January 30, 1990 -
A. No, I was not.
Q. Exhibit 1 of your deposition, which is your
bio that we discussed earlier -
A. Correct.
Q. -- says that you were the chairman of the
National Wildlife Federation's Corporate Conservation
Council. Did I read that correctly?
A. Yes, you did.
Q. And you're saying that that's not true?
A. That wasn't the question that you asked me.
Q. What did I ask you?
A. Let him repeat the question.
Q. It doesn't matter what I asked you. You will
admit that you were a chairman of the National Wildlife
Federation's Corporate Conservation Council?
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A. Yes. Q. Okay. Now, is that different from the National Wildlife Federation? A. Yes. Q. How are they different? A. This is a council. That is the federation. Q. But they're related? A. The council was an affiliated group that was sponsored by the federation. Q. Were you present at this January 30, 1990, meeting with the Corporate Conservation Council of the National Wildlife Federation? A. I don't believe so.
Q. Did you ever have any conversations with Mr. Mahoney about what he meant when he said. We, Monsanto, must rectify the mistakes of the past?
A. No. Q. Sitting here today, sir, do you believe that as part of his corporate goal, as stated at this meeting on January 30, 1990, that rectifying mistakes of the past would include removing PCB-contaminated sediments in Snow Creek, Choccolocco Creek, and Lake Logan Martin -
MR. PECK: Object to the form of the question. THE WITNESS: I think.
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BY MR. GRAMMAS:
Q. -- that Monsanto put there?
MR. PECK: Object to the form of the question.
THE WITNESS:
I think what his response would
have included was that Monsanto will take a
constructive attitude towards questions of prior waste
disposal and discharges and we will be an effective
player in the resolution of such issues.
BY MR. GRAMMAS:
Q. I'm going to show you what's been marked to
your deposition as Plaintiff's Exhibit 3. What is
that, sir?
A. It appears to be a copy of the speech that he
made at this meeting on January 30.
Q. What's the top of it say?
A. It says "Monsanto Pledge."
Q. And the first page says Page 1 of 2, and the
second page says 2 of 2. Do you recognize this
document as having come off of the web page that
Solutia has? A. That's what the heading says.
Q. Have you ever surfed this web page?
A. I've been on the web page. Q. Do you have the authority to approve what goes
on and what does not go on the web page with respect to
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environmental issues? A. I may review some of the things, but not all
the things. Q. The purpose of the web page is to allow the
public to, at their leisure, read what Monsanto chooses and Solutia chooses to put on the web page to educate them about the type of company Monsanto and Solutia is, right?
A. I mean, I think that's part of the purpose. Q. It's almost like sort of public relations-type information. A. I would say -- I would just more categorize it as information. Q. Right. And you certainly don't want any false information to be put out on a web page where millions of people can read it, do you? A. I wouldn't want any false information to be put out, period. Q. And that's because you don't want millions of people who may stop on the Monsanto web page to read information that does not accurately and truly and correctly reflect the company's position as it's described on the web page, right?
A. That's correct. Q. Now, this particular document that we got out
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is entitled "Monsanto Pledge" and it states here that:
"The Monsanto pledge was announced by chairman and CEO Richard Mahoney at a meeting of the Corporate
Conservation Council of the National Wildlife
Federation in Washington on January 30, 1990."
Did I read that correctly?
A. Yes.
Q. And then it says:
"Here is the pledge as
announced by Mr. Mahoney," and it starts off with a
series of quotes and paragraphs; is that correct?
A. That's correct.
Q. The tenth paragraph delivered to these folks
by Mr. Mahoney says what, sir?
A. "We must rectify the mistakes of the past
while we continue to develop and introduce the new
technologies to provide the essentials for mankind in
the future." Q. Now, are you testifying under oath today that
that does not include and it never was intended to
mean -- when Monsanto said "We're going to rectify
mistakes of the past," to remove PCB contaminants that
it placed in sediments in Snow Creek, Choccolocco
Creek, and Lake Logan Martin? MR. PECK: Object to the form of the question.
THE WITNESS: Two points; one for
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clarification, that the paragraphs of the pledge itself
are included in the first basically seven statements.
These quotes are part of the general communication
around that pledge.
Now, specifically to your question, I think
what this would basically say describes the process
that we're in that says that if there have been past
disposal or practices or waste for which Monsanto -
and we would say Solutia -- is responsible, that we
will be a proactive and constructive part of the
process to bring those to resolution.
BY MR. GRAMMAS:
Q. All right, but nowhere in that statement or
that pledge does he say what you just described, does
he? What he says in very simple, easy, and
understandable terms is, quote/unquote:
"We must
rectify the mistakes of the past."
A. I think what I'm giving you is basically the
practice that we had at Monsanto and we have at Solutia
that would implement that statement.
It would be wrong
for any officer or chairman to basically say we have an
open checkbook to the world for whatever anybody
alleges against the company, and that's what your
statement seems to imply. Q. No, sir, it does not, and I'm sorry if you
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interpret it that way. That's why -- see, originally I asked you if you felt it was a mistake for Monsanto to put the PCBs in this river system in the first place. Do you recall that question?
A. I believe I do and I think I answered it three times.
Q. I think you skirted answering it three times. I don't think I ever heard an answer.
MR. PECK: Listen Pete, you can ask him questions, you're not here to debate with him or to argue with him. That's all inappropriate. BY MR. GRAMMAS:
Q. I don't think I ever heard an answer - MR. GRAMMAS: Are you finished?
BY MR. GRAMMAS: Q. I don't think I heard an answer - MR. PECK: I heard an answer three times.
BY MR. GRAMMAS: Q. -- yes or no whether it was a mistake or not,
and because I never heard an answer, to my satisfaction, anyway, that it was a mistake, I presented you with Mr. Mahoney's statement that we must -- "we" being Monsanto not me, I didn't write these words, did I? These are Mr. Mahoney's words, aren't they?
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A. They appear to be. Q. These are the words that Solutia puts on a web page for millions of people to read at their leisure, right? A. I mean, the technical response is both web pages, because of the company's setup are both interchangeable, but those systems have now been separate and what you will find is that the Solutia and the Monsanto web pages, I believe, today are separate. Q. Okay. But on this document it says the Monsanto pledge and then there's the Solutia logo on the top right-hand corner of the page, right? A. That's correct. Q. So Solutia adopted the statements Mr. Mahoney made in here, too, haven't they? A. I think that we have very similar statements. We've not adopted those statements as they exist or were placed on the walls at Monsanto. Q. Does Solutia believe that it, like Monsanto, should rectify the mistakes of the past? A. I think I have answered that question, that - again, that basically says that we feel that where we have responsibilities and need to act in a responsible manner with respect to actions of the past, we will do so and we will do so proactively, not in an adversarial
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process.
Q. Do you believe, sir, that Monsanto has responsibilities to clean up the PCBs at Snow Creek,
Choccolocco Creek, and Lake Logan Martin, and now
Solutia?
A. I think if we continue our study work and it
determines that we have responsibilities as a result of
that, we will be there taking care of remediation which
is appropriate.
MR. PECK: Pete, let me tell you, this is an
additional document that I meant to produce at the
beginning of the deposition.
It's something that we
should have provided that is similar to things you
have, but when we searched Mr. Pierle's records, the
notebook that this was found in was at somebody else's
desk and it came up and we should have produced it.
MR. GRAMMAS:
I think you may have already
produced something like that.
(A SHORT BREAK WAS HELD.)
BY MR. GRAMMAS:
Q. In 1986, Mr. Pierle, you were named the
director of the environmental operations of Monsanto
Chemical Company; is that correct?
A. That's correct. Q. And that was an operating unit of Monsanto
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Company?
A. Yes.
Q. And your responsibilities, among others in that position, were to implement compliance programs
and cleanup of Superfund sites?
A. That's correct.
Q. How many Superfund sites have you worked with?
A. I think we have something on the order of 100
sites over time, maybe a few more where there have been
alleged Monsanto or Solutia responsibilities.
Q. How many of those sites involve PCBs? And if
you don't know the exact number -
A. My answer would be not many, very few.
Q. Tell me the PCB Superfund sites over which
you've had cleanup responsibility for Monsanto Company.
A. I don't think we've had any what I would
characterize "PCB Superfund sites."
Q. How many Superfund sites have you had cleanup responsibilities for for Monsanto that involve PCBs?
A. Again, I don't remember.
It's been a few.
Q. Could you tell me those locations?
A. The one I recall was a site in Texas called
Motco that had, I think, some levels of PCB material in
it.
I'm really struggling.
I don't recall any others
where PCBs were a significant question or issue.
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Q. Has Monsanto been involved in any Hudson River PCB remediation?
A. No.
Q. Are you aware of any issues relating to PCBs
on the Hudson River?
A. Yes.
Q. How are you aware of those?
A. Through the general literature and
understanding of Superfund cases.
Q. Motco, was that a customer of Monsanto's that
purchased PCBs?
A. No. Q. Why is it Monsanto is involved in PCB
remediation in Texas?
A. We were involved in the remediation, which
included PCBs, at that site.
I didn't say that they
were Monsanto PCBs and that's why we were involved.
Q. Why were you involved with that site at all?
A. It was a materials reclaiming site that was
owned by multiple and succeeding owners that was
reclaiming basically styrene tar materials, and the
owner basically took a hike, and through the sort of
pre-Superfund and Superfund investigative process, it
was determined that some of those materials had
originated at Monsanto sites and that brought us into
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the involvement at that location.
Q. Some of those materials included PCBs, right?
A. Again, there were materials at the site that
were PCBs, again a small amount.
I don't recall
whether those were ever part of Monsanto's
responsibility.
Q. What role did you have in drafting the
environmental guidelines back in the 1989 time frame
through today, both for Monsanto and now Solutia?
A. Well, I've been involved in the process, to
varying degrees, in reviews and rewrites as part of my
job responsibilities and led the rewrite in Solutia as
we became a separate company.
Q. Now, the environmental guidelines for Solutia
are still in their draft form, correct?
A. We have finalized those.
Q. The document that I see, and we'll talk about
it in a minute, is Solutia's commitments manual.
Is
that what you're talking about?
A. No. I think that is a -- what I referred to
was the commitment statements themselves, the six
commitment statements which are the broad policy
statements, I believe are complete.
Q. You're talking about -- not to interrupt you,
but just so the record's clear, you're talking about
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these six statements right here? A. That's correct. MR. GRAMMAS: Let's go ahead and mark that. (PIERLE EXHIBIT NO. 4 WAS FIRST DULY
MARKED, RECEIVED AND MADE A PART OF THE RECORD.) BY MR. GRAMMAS:
Q. Plaintiff's Exhibit 4, could you identify that for me, please, sir?
A. This appears to be a document, again taken off of the Solutia web site, which states Solutia's environmental health -- or, environmental safety and health commitments, and there are basically six statements.
Q. Those are the broad policies that dictate Solutia's environmental conduct?
A. That's correct. Q. All right. Now, Solutia commitments manual, dated June 9, 1998, with a big "Draft" stamp on it, it's about two inches thick and it's got "Draft" written on every page, what is this? A. That is a document that is intended to further really expound upon these statements and to delineate for us guidance and requirements and practices to be followed within Solutia.
(PIERLE EXHIBIT NO. 5 WAS FIRST DULY
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MARKED, RECEIVED AND MADE A PART OF THE RECORD.) BY MR. GRAMMAS:
Q. Now, I've identified this as Exhibit No. 5,
the June 9th document that you were just describing.
This document, Exhibit No. 5, has not been implemented
yet; is that correct? It's still in the draft phases?
A. The document is in its draft phase. It
represents, though, many of the practices that were in
existence and documented at Monsanto; and therefore,
many of these are in practice today, but perhaps not
all, because indeed what we're trying to do is to
tailor this specifically to Solutia's businesses.
(PIERLE EXHIBIT NOS. 6 AND 7 WERE FIRST DULY
MARKED, RECEIVED AND MADE A PART OF THE RECORD.)
BY MR. GRAMMAS:
Q. We're going to talk about them in a minute.
Plaintiff's Exhibit 6, sir, looks to me to be
a document created sometime around May 22nd, 1989,
according to a cover letter attached to worldwide
guidelines that Monsanto followed on environmental
safety and health guidelines.
Is that a correct
statement? A. You did say '89?
Q. Yes, sir.
A. Yes.
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Q. And Plaintiff's Exhibit No. 7 is a similar
type document, with a different cover letter, dated
November 11, 1992, which I believe in prior depositions
have been -- has been described as an updated version
of the 1989 guidelines; is that correct?
A. I think that's accurate.
Q. Now, what involvement did you have in drafting this 1989 and this 1992 environmental safety and health
guidelines for Monsanto?
A. Again, I was an active participant at both
times.
In the '89 document I would have been in the
chemical company, so I would have been looking at,
reviewing, and participating, along with others, in the
development of this. And again, this was a revision of the further -- of a prior version itself.
And in this case, in '92, I had less of a
hands-on, you know, working with this as opposed to
sort of getting a process underway to update these and
to include basically what was inclusive of the Monsanto
pledge.
Q. Now, you had a fairly involved role in
drafting, creating, and making sure that these
guidelines for Monsanto were implemented and followed
by the plants that fell under the Monsanto Company,
right ?
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A. That role changed from time to time. in the '89 time period, it included implementation; whereas, in '92, in a corporate role, the direct implementation was again up to the operating units, and the role of myself and the corporate staff at that time was one more of oversight.
Q. On November 11, 1992, you wrote to Monsanto employees distributing the 1992 updated version of the guidelines, right?
A. That's correct. Q. Now, in this November 11 letter you write to Monsanto employees that the Monsanto pledge serves as the umbrella for Monsanto's overall environmental safety and health programs, right? A. That's correct. Q. And in support of that commitment, you developed this -- what you refer to as the Monsanto pledge guidelines, right? A. That's correct. Q. And these guidelines replace the guidelines from the environmental safety and health guidelines, which is Exhibit 6, right? A. Assuming this was the version that was in effect at that time, because this one does not refer to the '89 document specifically.
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Q. But it does refer to environmental safety and health guidelines, which are the bold words contained on the very first page of the 1989 document, right?
A. Yes. Q. And you state in here that the November 11, 1992, Monsanto pledge guidelines set forth the management expectations for environmental safety and health performance, correct? A. Correct. Q. And that these guidelines describe key results against which progress will be measured, right? A. That's correct. Q. Were you a member of the environmental policy committee that approved these guidelines? A. Yes. Q. So you voted in favor of implementing the Monsanto pledge guidelines; is that a fair statement? A. Yes. Q. Now, you direct all Monsanto employees that received a copy of these Monsanto pledge guidelines to conform with the spirit of these guidelines, correct? A. Yes. Q. In fact, you say that conforming with the guidelines is not -- strike that.
You say that they don't have a choice in
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whether they can conform or not conform, right?
A. I think what it says specifically, and I'll
read it:
"Conformance with the spirit of the
guidelines is not optional, although considerable
latitude and innovation is expected in tailoring the
guidelines for specific operating units."
Q. Okay. You direct these employees to follow
these guidelines in a non-optional fashion, right?
A. Again, it's important to make the distinction
that says what the spirit of the guidelines are and
what that then says is that you are expected to be
smart and innovative and there is latitude in tailoring
the guidelines for the specific operating units.
Q. Did the latitude -- and by the way, who has
the latitude in tailoring these guidelines, plant
manager? A. I think that would depend upon what the
particular issue was within the guidelines. They would
not have latitude to change policy, but within here
they would have latitude on implementation of programs,
timing of results, things of that nature.
Q. Would you consider the Monsanto pledge an
environmental policy?
A. The high-level statements within the pledge
itself would be generally considered to be the policies
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that we expect people to operate under. Q. And if the jury believes, based on Plaintiff's
Exhibit 3, which is entitled the "Monsanto Pledge" that we've just identified in your deposition, that part of the pledge was for Monsanto to rectify mistakes of the past, that would not be something that, say, a plant manager in Anniston could just willy-nilly ignore, correct?
A. I think I made it clear that that particular statement that you referred to is not part of the Monsanto pledge.
Q. And is that because Monsanto, and now Solutia, does not believe that it should, as one of its environmental policies, rectify mistakes of the past?
A. That's not what I said. I think what I said on a factual basis is that the first seven statements deal with what the "Monsanto pledge," as it came to be called, was the direction provided the employees as policy direction.
Q. You had the authority of setting policy, environmental policy for Solutia and Monsanto when you held that position there, right?
A. I could not unilaterally set policy, no. Q. You mean to tell me if you felt like a good policy for Monsanto, and now Solutia, to have is to
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rectify mistakes of the past, you couldn't ensure that that policy was implemented?
A. What I'm saying to you is I do not have unilateral authority within the structure to do that.
Q. Again, in the 1989 environmental safety and health guidelines, who is Mr. Corbett, H.J. Corbett?
A. He was at that time the senior executive that had responsibility for environmental health and safety and some other functions.
Q. So he basically was your predecessor at Monsanto?
A. Well, he held the position -- it was at sort of a little bit different level and different scope, but with respect to environmental safety and health matters, he was a former leader of that area.
Q. And in 1992 you wrote the letter distributing the Monsanto pledge guidelines, right?
A. That's correct. Q. And based on his similar position as you, in 1989 he wrote the letter distributing the environmental safety and health guidelines? A. That's correct. Q. Now, it was also his instruction that the employees of Monsanto, it was not optional for them not to follow the spirit of the guidelines implemented,
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correct ? A. If I could review the document. Yeah, it says compliance with the spirit of
the guidelines is not optional. Q. And you received these guidelines, did you
not ? A. That's correct. Q. And you, like every other employee, were
required to follow these guidelines, too, in setting your environmental policies, right?
A. Again, the spirit of those guidelines, that's correct.
Q. Now, the words contained in these guidelines have significant meaning, do they not?
A. Yes. Q. And these words were not empty promises that Monsanto made in an effort to trick people into believing that they were concerned about the environment, were they? A. No. Q. The promises made in these guidelines were self-imposed obligations that Monsanto, as an environmental policy, committed to follow, correct? A. Again, the guidelines contain sort of two or three different levels. One is a set of policy that
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sets the conduct and behavior. There are programs and specifics that were at that time intended to represent what we were doing and we were serious about those, that's correct. But in some cases, the programs or the dates and things changed as things became practical to do or impractical to do or for other reasons.
Q. But the bottom line is, sir, these guidelines set the standards, promises, duties, and responsibilities of Monsanto and its employees to its stakeholders, correct?
A. I would say that what was set specifically and communicated to the public were the high-level policy statements. The balance of it and the more specific guidelines were the internal programs that were evolving and being developed. So there's a slight difference there.
Q. There is a slight difference, and I don't mean to be confusing and I appreciate you being clear in your answer, but we'll limit it to what was set in stone to the policy guidelines, okay? Those policies were self-imposed standards that Monsanto expected and demanded its employees to follow, right?
A. That's correct. Q. Now, Solutia has not as of yet adopted the more detailed standards that we find in Plaintiff's
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Exhibits 6 and 7 because Solutia's basically still in draft form, right?
A. I think what we have said is to the greatest extent, we should continue to use the content of these guidelines as the direction until they are replaced with a new set of guidelines.
Q. You read my mind. That's where I was going next. So until the new guidelines are replaced, Solutia's required to follow the Monsanto pledge guidelines contained in your November 11, 1992, letter, right?
A. Yeah. Again, in reading the statement, that those at the time in '92 said that latitude and innovation was expected in tailoring the guidelines for specific operating units. So, to an extent that qualifier still exists today.
Q. Right. Same exact expectations of Monsanto in 1992 apply today to Solutia as far as these Monsanto pledge guidelines are concerned?
A. Again, just to be clear with respect to our policy statements and guidance, those have been cleared and clarified in our commitment statements and to the extent that these set out, you know -- guidelines are what they are. Guidelines are things that basically - you know, they're intended to be developed to be
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followed, the spirit of the guidelines. So part of it is if the guideline doesn't apply to you, then obviously you don't follow it.
Q. Right, but if it does apply to you, you do follow it.
A. Unless you have some situation or set of facts that says, you know, that for some reason it's not - you're not able to do it.
Q. Okay. Now, when some individual manager of a plant or some individual low-level employee is faced with a decision about whether or not to follow one of these guidelines and makes the decision that it is not required to follow it, for whatever reason, because under the spirit of the guidelines, he feels like he doesn't have to, what must he do in order to not follow the guidelines, if anything?
A. Your question confused me because you said "under the spirit of the guideline, he feels he doesn't have to do it." I think what this document says is that if it's under the spirit of the guideline and that would be his understanding, then the person would have to do it.
Q. What I meant to say was, I interpret that sentence -- when you talk about "spirit of the guidelines," it's both in your November letter and in
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Mr. Corbett's May 1989 letter -- that following the
spirit of these guidelines is not optional.
A. That's correct.
Q. That means there's some leeway -- or does it
mean, rather, that there's some leeway that managers or
lower-level employees have to not follow these
guidelines?
A. Again, let me make two comments. One, if they
felt that there was an issue with respect to the spirit
of the guideline, they would bring that issue back up
through the process to the policy committee at which
time there could be a consideration to change the
policy and a specific guideline.
If the individual was
following, in their minds, the spirit of the guidelines
but was doing it in a different way or doing something
slightly different that was still within the spirit,
then they may have the authority just to do that
themselves or, within their unit, have a different
process for making that decision.
Q. I think we're on the same page. Really what I
want to know is, Mr. Pierle, if some lower-level
employee, or any employee, for that matter, makes a
decision that they're not going to follow these
guidelines, what must they do to bring that to the
attention of Monsanto, and now Solutia, if anything?
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A. Well, again, if it's the spirit of the
guideline, they would bring that probably back up
through their sort of chain of command, to use a common
expression, for consideration.
If it dealt with
specific execution of a portion of this which is
defined as optional, then they may feel free to make
that decision on their own.
Q. And if it dealt with a portion of what is
defined as not optional and they wanted to not follow
it, what would they have to do?
A. I think they may have the ability -- again,
not on a policy matter, but they may have the ability
to say, That doesn't apply to me; therefore, I don't
have to follow that specific -- that specification.
Q. We're almost there. We're almost there.
A. So they can make that judgment themselves.
Q. We're like this close to where we need to be,
but we've got to jump that next hurdle to get to the
last statement, Mr. Pierle. There may be situations
where some employee feels like they don't have to
follow it, but yet according to the guidelines, it's a
non-optional category. Do you see the conflict now?
The employee thinks, I don't have to follow it; when,
in fact, you, as the highest-level manager would say.
No, you're wrong, you'd better follow that.
In that
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situation, what must the employee do to bring it to
your attention or someone else's attention, if
anything?
A. I think I described that they would bring that
situation -- we would hope they would bring that
situation back up through a chain of command or through
their plant people or business people, or whatever,
back to say, I've got an issue here that we need to
discuss.
Q. What happens if you become aware of employees
or plants ignoring the policies that don't fall within
some of these exceptions we're talking about, they just
violate the policy stated in the -
A. We have a very aggressive audit program that
we have had since 1980 that basically looks at the
conformance with external requirements and internal
requirements. The results of those audits are
tabulated and actions are put in place to, you know,
rectify or improve the situation.
If, in that process,
there was a discovery of an employee who had blatantly
disregarded it, it could be subject up to dismissal of
the individual.
Q. Are you aware of that ever happening, and in
particular at Anniston? A. I don't know whether it has or hasn't.
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Q. Would that be something that would normally come to your attention at the level you're at?
A. Not necessarily. Q. All right. Now, what, in your mind, sir, does someone have to do to prove to you, as the lead environmental manager over remediation, that your company is fairly established as a responsible party for causing pollution or contaminants in general? A. Again, I think there has been an evolution of definition around that responsible party. Q. And I don't mean that in a term of art. Okay? What I want to know is: What does the government or a person just bringing something to your attention or a plaintiff suing Monsanto, and now Solutia, have to do in your mind -- not legally, but in your mind -- to prove to convince you that your company's conduct was fairly established as the source of pollution? A. I think there would have to be a factual presentation that basically not only were our materials there, but it was a result of some action that was assignable or definable to the company. Q. Okay. If, for example, they showed you, as the environmental manager chief over remediation, that one of your plants discharged thousands of pounds of PCBs into a river system and that they were finding
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concentrations of the PCBs, both in the sediment and in fish, and that there was no other apparent source of PCBs, would, in your mind, that fairly establish that Monsanto was the party responsible for putting it there?
MR. PECK: Object to the form of the question. THE WITNESS: You had too many hypotheses in there. BY MR. GRAMMAS: Q. We'll break them down. All right. If the person showed you, through evidence, that Monsanto discharged thousands of pounds of PCBs for close to 40 years, we'll just say approximately 40 years, into a river system -- you got that hypo? A. Yes. Q. -- and no apparent other source remotely close to Monsanto discharged that quantity of PCBs into the river system -- are you with me? A. Yep. Q. -- and finally, that concentration levels of PCBs are being found in fish in the river system and in sediment in portions of the river system, those three things are shown to you to exist -- and I can repeat them if you want to because we were kind of going slow writing them -- in your mind, if you were faced with
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those three facts, sets of facts, would you believe that that person who presented you those facts has fairly established Monsanto as being a responsible party for the source of the PCBs in the river and fish?
MR. PECK: Object to the form of the question. THE WITNESS: I think not necessarily, but it would sure cause me to want to understand answers to some additional questions. BY MR. GRAMMAS: Q. Tell me, Mr. Pierle, as the head environmental manager over remediation for Monsanto, what a person has to show you to fairly establish -- notice I didn't say "conclusively" establish that you were the source, I just said "fairly" establish that you're the source, what in the world does somebody have to prove to you to establish that you would be the source of PCBs in the situation I've just described to you? A. I think what I said was that that would cause me to feel that there's enough information that says we're probably there. But within that, I would say there are more things that I then want to understand with respect to that site and the facts around that that would help me to understand then what -- you know, how fair is that and how extensive is it? Q. But under those facts, yes or no, would that
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fairly establish in your mind that you're a source that would then prompt you to do some other things?
A. I think what I said is that that would cause me to make sure we were involved in understanding, then, the extent and whether there's an issue there or not.
Q. And you, based on your own guidelines, sir, know that once those things are fairly established, your role is to immediately get involved in that process, don't you?
A. I think under different laws that, you know, you could or you couldn't.
Q. Well, we're not talking about laws, we're talking about the self-imposed guidelines, sir, that you had a direct hand in making.
A. And I think what I said is that that would cause us to get proactively involved in further understanding that and that we would do that and that's exactly the path that we're following. That's why we've such extensive investigations and studies underway right now in cooperation with ADEM and others down there to understand what the factual situation is.
Q. Sir, your obligation under Monsanto guidelines, the health and safety guidelines in 1989, was to immediately get involved as soon as you became
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aware of those issues being fairly established, true?
A. Yes, and I think we have.
Q. Now, is "immediate," in your mind, waiting 30
years to do something about it?
A. You are again asking a question that wasn't 30
years. Number one, you know, the guidelines aren't 30
years old. So you're confusing the question. You're
certainly confusing me.
I think what the guideline
says is that based upon our experience that produced
those guidelines, was that with respect to looking at
retroactive actions and things that happened, that
Monsanto would take a position, and Solutia, to get
immediately involved in that process, not to stand back
and say, We're not involved, go away, come back. And
that's exactly the guidelines, the spirit of the
guidelines, and that's exactly what we're doing.
Q. Okay. When you say "immediately," what does
that mean to you? To me it means whoa, we've done
something, let's do something to figure out what's
going on and fix this problem. That's what
"immediately" means to me, the second you become aware
of it. What does it mean to you? A. Well, I'll give you an example at another
site, a Superfund site, like Motco and others, we
became immediately involved in the process.
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Q. Let's talk about Anniston.
A. That process has gone ten to 12 years. In many of these, immediate involvement leads to a process
that, through no fault of anybody, is extremely
extensive.
So that's what "immediately" means to me.
Q. And that would apply in Anniston, Alabama.
A. And I think that's exactly what I've described
and what we've done.
Q. And if you became aware in the '80s that there
was PCB contamination because the attorney general told
you that they were finding high level of PCB in Snow
Creek, it was your responsibility at that time to take
immediate action to remediate not only what the
attorney general found, but to start this process that
you started four years later, and you're doing eight,
ten years later, to determine what impact your
discharges may have had on the river system, right.
MR. PECK: Object to the form of the question.
THE WITNESS: Again, what you described in
'85, we got immediately involved with the extent of the
problem that was defined and we stayed through it
through the remedy of that issue.
BY MR. GRAMMAS: Q. Sir, you did not do anything other than
remediate the upper portion of Snow Creek, which is
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what I believe the attorney general asked you to do, right ?
MR. PECK:
I object to the form of the
question.
THE WITNESS:
I'm not familiar with what the
specific -
BY MR. GRAMMAS:
Q. And you didn't start looking into this more
pervasive study, this process you've been describing,
until around 1993 -
MR. PECK: Object to the form of the question.
BY MR. GRAMMAS:
Q. -- when the Alabama Power personnel brought to your attention PCBs were leaching from property you had
given it 30 years earlier, right?
MR. PECK: Object to the form of the question.
THE WITNESS: We didn't give them the
property. They bought the property with knowledge of
what was there. So, again, your factual statements in
your question are -
BY MR. GRAMMAS:
Q. You-all didn't begin this process that you're
currently in until 1993.
A. Thereabouts. Q. You will admit that that's four years after
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this remediation you did on the upper portion of Snow Creek.
A. It is, but it's also immediately upon discovery of a situation, as I say, with a landfill and the runoff question that we have continued to stay with.
Q. How long does it take to do a study like this? If you started in 1993 and your sole focus was to determine the exact impact of what these PCBs were doing to the environment, if anything, how long does it take?
A. Again, what I've described is that through a process that's been open and with the regulatory officials, we have been in a stepwise process to understand what the factual situation is; and unfortunately, I guess that takes a long time. But the reality is we're moving as fast as we can with respect to sampling, understanding, determining remedies, dealing with sources of problems, and doing this in a very responsible way.
Q. Okay. And the first step you took was to clean your own property, wasn't it, sir?
A. I think the first step, an accurate characterization of that, was to deal with what was defined at that point in time as a potential source of
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PCB into Snow Creek, and that involved part of our
property, but almost immediately, as well, took us to
property that was adjacent to the plant site and we
were just as quickly dealing with property owners
adjacent to the plant site.
Q. The first step Monsanto took, in your own
words, sir, was to clean up its own backyard, right?
MR. PECK: Object to the form of the question.
Those were never his words.
THE WITNESS: Those are your words.
BY MR. GRAMMAS:
Q. I'm asking you. Do you understand what I'm
asking?
A. You're not asking me.
I told you "no" to that
question.
Q. That was not the first thing you did. You-all
hadn't cleaned up your own backyard as we sit here
today; is that what you're telling me?
A. What I'm telling you, we've undertaken several
actions, which include actions with respect to property
we own, with respect to properties that we do not own,
because that was -- the collective judgment is that's
where the priority actions should occur.
Q. Collective judgment of whom?
A. Of the people involved in the process.
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Q. And that would be Monsanto people?
A. Including the regulatory people. The public
is certainly aware of this and there's been an open
conversation about the steps and the actions that are
appropriate.
Q. Now, how large of a company in terms of
dollars in revenues is Monsanto?
A. Are you asking Monsanto or Solutia?
Q. Monsanto, and now Solutia. But at the time
this was happening, Monsanto, back in the late '80s,
early '90s. How many billions of dollars did it
generate ?
MR. PECK: Object to the form of the question.
Irrelevant.
MR. GRAMMAS:
It's not irrelevant.
MR. PECK:
It's absolutely irrelevant.
It's
not coming into evidence. You can ask him the
question, but it's not coming into evidence.
MR. LOWE: At what stage?
MR. PECK: At any stage. We haven't changed
the law in Alabama to allow that stuff into evidence
yet, guys, and I don't think our current Court's going
to do that.
MR. GRAMMAS: Okay.
MR. LOWE: There's an election later.
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THE WITNESS: Am I instructed to answer? MR. PECK: If you know what he's asked you. BY MR. GRAMMAS: Q. What's your gross revenues approximately in this time period for Monsanto, just approximately? A. About $8 billion. Q. What were the profits in that time period? A. I don't know. Q. Roughly. A. I don't know. Q. You have no idea? A. No, I don't. Q. Billions of dollars, though, would it not be? A. I doubt that. I don't think the company's ever made that much in a year. Q. Certainly there was no financial impediment, Mr. Pierle, that you're aware of, as the senior environmental over remediation, for Monsanto to look into the issues of PCBs on its property and the neighboring properties and simultaneously do this study downriver to see how bad Monsanto may have affected those properties, was there?
MR. PECK: Object to the form of the question. THE WITNESS: And I think I've said, typically
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the process that you get into here, and it's very common at cleanups everywhere in the United States, is that you look at these things and segment it in piece fashion, and that's exactly what we're doing. BY MR. GRAMMAS:
Q. Okay, and my question to you had nothing to do with your answer, in all due respect, sir. My question to you was: From a financial perspective, was there anything that you're aware of that prevented Monsanto from doing it simultaneously?
A. And my judgment is that's not a relevant question.
Q. Well, I don't care what your judgment of relevant is, quite honestly.
MR. PECK: Let him answer. BY MR. GRAMMAS:
Q. You have to answer the questions I ask, and the question is: Was there anything of which you were aware from a financial standpoint, as the environmental manager over remediation for this entire process from start to finish, that would prevent Monsanto from simultaneously looking at PCB-related issues on its property and at the same time look at it in Snow Creek, Choccolocco Creek, and Lake Logan Martin?
MR. PECK: Pete, he's right. You're being
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subjected to having to answer his questions, but you
can answer his question however you need to honestly
answer it.
BY MR. GRAMMAS:
Q. And I want you to answer it honestly, Mr.
Pierle.
A. That to me is not a relevant question in the
process. What is relevant about that when faced with
that set of circumstances is: Are we proceeding on
what is appropriate and relevant to the question? And
in almost all cases, that process starts with: What
are the priorities that we need to do here? Is there
anything imminent that is a problem to the health or
the environment? If so, you do removal. No, there's
no imminent issue that needs to be dealt with.
So what
do you do at that point in time? You then say: Let's
investigate what we understand, then, the depths of the
problem to be and the steps that need to be taken. And
that is precisely what we are doing.
MR. GRAMMAS: Adam, would you please confer
with your witness and ask him to answer the questions
that I'm asking.
I understand he -
MR. PECK: He's answering the questions you're
asking, you just don't like the answers.
MR. GRAMMAS: Adam, he didn't. He says it's
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not relevant and I'm not going to answer it.
I want to
know a simple question: Did they have any financial
impediments to do them both at the same time? I'm not
asking him why he didn't do both at the same time, and
I'm entitled to an answer to that question, Adam.
MR. PECK: Then ask him the question.
If you
don't like his answer, ask him again, but I'm not going
to instruct my witness how to answer your questions.
I
don't particularly like your questions.
I don't like
the tone with which you ask those questions, I don't
like the tone with which you treat my witnesses.
I
don't like anything about it and I'm not going to
instruct him how to answer the questions.
I'd just as
soon walk out.
MR. GRAMMAS: I'm sure you would.
MR. PECK:
I would.
I'm not used to people
treating my witnesses so impolitely.
MR. LOWE: How many have we taken?
MR. PECK: Well, that's true. The ones that
Pete's taking, I'm getting used to him treating my
witnesses impolitely. Not so much Clay, but Pete
generally, you're right.
BY MR. GRAMMAS:
Q. Mr. Pierle, I'm here to ask you questions and
I'm sorry if I'm being impolite to you, but when I
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don't get answers or I get nonresponsive answers, I
don't accept that as an alternative.
I'm doing my job
and I understand you're here doing your job. All I
want to know is: Are you aware of any reason,
financial or otherwise, that would prevent Monsanto at
that time from doing remediation work on its property
and on the neighboring properties? That's the question
that I'm asking you.
A. And my response was that is not a question
that we ask ourselves. So how can I respond to it? To
us, in that process, that's not part of what you ask
yourself up-front.
Q. So the answer is: You don't know the answer?
You don't know the answer to that question?
A. I think I've answered the question to the best
of my ability.
Q. Are you aware of any reason why Monsanto could
not have cleaned up its property and the neighboring
properties simultaneously? Are you aware of any
reason?
MR. PECK: He's answered that question three
or four times.
If you must have him answer it again,
he'll answer it one more time.
BY MR. GRAMMAS:
Q. Are you aware of any reasons, sir?
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A. I don't know how to answer your question any
better than what I've answered it up to now.
MR. PECK: How long is this going to go? Are
we going to need to take a lunch break?
MR. GRAMMAS: Adam, that is a very central
question and it deserves an answer.
MR. PECK: He just answered your question.
MR. GRAMMAS: He said it's not relevant to me,
so I don't know the answer to it.
That's fine, let me
hear him say "I don't know."
MR. PECK: You've heard his answer.
MR. GRAMMAS: No, I haven't.
MR. PECK: You've heard his answer.
MR. GRAMMAS: No, I haven't.
I've heard his
answer, but it hasn't answered the question.
I mean,
it's a fair question, Adam.
MR. PECK:
I'm not going to instruct my
witness how to answer your questions, Pete. That's
not -- that's not my job here.
MR. GRAMMAS: Do you think the question is a
fair question?
MR. PECK: No, I don't think it's a fair
question. MR. GRAMMAS: Why is it not fair? Tell me so
I can cure it.
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MR. PECK: Because he has told you that's not what they even ask themselves. They don't even ask themselves that question.
MR. GRAMMAS: That doesn't matter whether they ask or not. Maybe they should have asked themselves that, Adam.
MR. PECK: Well, no, because it wasn't relevant. They didn't even consider the financial issue. That's the answer to your question. They didn't even consider it.
MR. LOWE: Let's move beyond that. Why couldn't you do it simultaneously, period?
MR. PECK: Are you going to ask that question? MR. GRAMMAS: I've already asked it three times, is there any reason why it couldn't be done simultaneously? I've asked it three times. MR. PECK: No, you haven't asked that question three times. You've asked if there was a financial impediment. MR. GRAMMAS: Let's not argue, Adam. MR. PECK: Are we going to have a lunch break or not? MR. GRAMMAS: Yeah, after we get the answer to the question. MR. LOWE: Seven minutes to 12. He's got
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seven minutes to answer the question.
MR. LOWE: What's the question?
MR. PECK: Why couldn't you proceed with doing
Snow Creek, Choccolocco Creek -
MR. LOWE: No, no, no, the question is -
MR. PECK:
-- at the same time you did the
plant site remediation?
MR. GRAMMAS: No, that's not the question,
Adam.
MR. PECK: Well, then ask your damn question.
MR. GRAMMAS:
I'm going to.
I've asked it.
MR. PECK:
Is Clay asking the questions or are
you asking the questions? I think we're entitled to
one person asking the questions and you choose it to be
you.
MR. GRAMMAS: I'm asking the questions, Adam.
Clay hasn't asked any questions.
MR. PECK: Ask the question. Ask the
question. We're going to answer that question and
we're going to go to lunch.
MR. GRAMMAS: I agree. The question is the
same as it's been.
MR. PECK: Ask it.
MR. GRAMMAS: Adam, don't scream at me.
MR. PECK: Ask it.
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MR. GRAMMAS: Don't scream at me.
MR. PECK: You've been screaming at my witness.
MR. GRAMMAS:
I have not raised my voice a
single time. Now, you may think my manner may be
impolite --
MR. PECK: I do.
MR. GRAMMAS:
-- but I haven't raised my voice
to your witness.
I haven't raised my voice to you.
Don't scream at me.
MR. PECK: Ask the question.
MR. GRAMMAS:
I don't want to hear that.
MR. PECK: Ask the question.
BY MR. GRAMMAS:
Q. Is there any reason, Mr. Pierle, why the remediation could not be done simultaneously on your
property at Monsanto's Anniston site and on my
plaintiffs' properties, or at least looked into
simultaneously?
A. And I answered that question, that in looking
at what was known, what was needed to be understood and
known, whether or not there was an immediate reason for
the removal or a quick go-do-something action, that did
not exist. So what needed to happen, and this is very
typical, is you have to go about a more methodical
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process to understand what is the problem, is there a
problem, what needs to be done, what are the
remediation options, what are the technology options,
and you tend to do that in a way that looks at priority
first. And whether it's the right priority or not,
generally what you do is say, Where might there be
potential sources, what action can we do relative to
that, and that's where you go focus your attention.
Then you still have to deal with the issues, Well, now,
what else might there have been as a result of that? I
mean, that's the process that we're in.
It's very
typical.
It's generally been assumed to be a right in
areas where we and many others are dealing, and I think
that's the answer to the question.
Q. Okay. I didn't hear you mention the word
"finances" in there at all.
Is that because finances
did not play a role in this decision to clean up
Monsanto's property first?
A. And my response to that was that we don't ask
ourselves, you know, what is it going to cost, what -
can we afford to begin or not.
I think, as our
guideline said, we will immediately get involved in
understanding what the issue is and the definition of
the issue, and that's exactly what we're doing.
Q. And cost to Monsanto, and now Solutia, is not
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__________________________________________________
an issue it considers in deciding whether to clean up
PCB-contaminated sediment that it is possibly
responsible for causing?
A. That's not what I said.
Q. I'm asking you that.
A. Cost is a very relevant factor in the
selection of remedies and in the options that get
looked at. So, yes, cost is a very relevant factor in
every decision that gets taken by anyone with respect
to a remediation action.
Q. Do you believe, sir, that at this site, the Snow Creek/Choccolocco Creek/Lake Logan Martin site
immediately downstream from your plant that
manufactured PCBs over these periods of decades we've
talked about today, that you-all are not the, but a
major contributor to the PCB concentrations that are
being found in this river system?
MR. PECK: Object to the form of the question.
No foundation.
THE WITNESS:
I mean, again, I thought we had
sort of covered this ground in a prior conversation and
questioning where I said, you know, that we are there
because there is factual information that says it's
important for us to be part of this solution at this
site, which means that there is a probability that we
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_______________________________
have some responsibility. What we're about is trying
to determine is that in fact real and what is the
extent of that.
BY MR. GRAMMAS:
Q. Now, when this probability existed you have
some responsibility, is it your opinion at this point
in time, sir, that you will not delay cleanup by
unnecessary legal yet negatively perceived litigious
steps ?
MR. PECK: Object to the form of the question.
He's quoting from a section of the guidelines, and if
you want to ask him about that section, show it to him.
BY MR. GRAMMAS:
Q. You can answer the question.
A. It's very clear that we are committed to
pursuing the process that we're in to its completion,
and that although we'd never give up a legal remedy,
which you wouldn't advise me as my counsel to do that,
our priority on these is to try to work through these
in as acceptable a manner as we can, such as to get on
with solving a problem if it exists, not worrying about
litigating and delay.
Q. Right, but my question, though, is a little
more simple than that, Mr. Pierle.
My question is:
Is
it your position that you are not going to delay
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cleaning up the PCB problem through unnecessary legal
steps?
A. And I think I answered that and that -- just
as I described, that we are moving through that with
the anticipation that we will get through a process and
understand whether there's a problem that needs
remediation, what the extent of that is.
If we have
obligations, what obligation that is and how can we be
part of that solution. That does not mean that if
there is an outrageous under -- determination by
someone that a remedy is wholly inappropriate for what
the solution is, that if we have legal remedies
available to us, that we will not pursue those. We are
looking for a remedy as a priority.
Q. Do you believe, sir, as the head of
environmental management over remediation for Solutia
and, in the past, for Monsanto, that Monsanto's
responsibility for the PCBs in Snow Creek, Choccolocco
Creek, and Lake Logan Martin, as we sit here today,
have been fairly established?
MR. PECK: Object to the form of the question.
BY MR. GRAMMAS:
Q. As has that word as stated in your 1989
Worldwide Guideline No. 2 under a heading called "Waste
Management," Section 4, "Corrective and Remedial
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Action."
MR. PECK: Do you want to show him that?
MR. GRAMMAS: He's read it. He's seen it. He helped write it.
BY MR. GRAMMAS:
Q. Do you believe that your -- that Monsanto's,
and now Solutia's, responsibility for the PCBs in Snow
Creek, Choccolocco Creek, and Lake Logan Martin have
been fairly established, as those words mean under that
guideline?
MR. PECK: Object to the form of the question.
MR. GRAMMAS:
I've got one more question and
then we can take a lunch break.
THE WITNESS: I think, by the words of the
definition of this guideline, we're not at this step of
having responsibility fairly established.
BY MR. GRAMMAS:
Q. Now, what is being done by Monsanto, or now
Solutia, at Choccolocco Creek, Snow Creek, and Lake
Logan Martin to convince you that you are not a source
of PCBs that are being found there, if anything?
MR. PECK: Object to the form of the question.
THE WITNESS: You know, there is an extensive
study underway looking at the hydrology of the system, the sources, potential sources, and that report will be
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instrumental in helping to -- for us to understand our
responsibilities or the extent of those with respect to
what you've described.
I think we've said on Snow
Creek, you know, we've already demonstrated a
responsibility there, and I think the work that is
underway will go a long way towards defining if there
is additional responsibility.
MR. GRAMMAS: Okay.
MR. PECK: Lunch?
MR. GRAMMAS: Yes.
(LUNCH RECESS.)
BY MR. GRAMMAS:
Q. Mr. Pierle, has Monsanto completed the cleanup
work in and around the plant and the neighboring
property for PCB cleanup?
MR. PECK: Did you ask "completed"?
MR. GRAMMAS: Yes.
THE WITNESS:
I don't think all that work is
done yet.
BY MR. GRAMMAS:
Q. Has Monsanto determined who put the PCBs
there?
A. I think, with respect to most of that, we just
accepted the fact that it probably came from us and,
you know, with enough work around, how it may have got
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there and sort of moved on per our practice here and
took over accountability for it and have moved through
remediation in most of the areas.
Q. Are you sitting here today, sir, any less than
100 percent certain that Monsanto's PCB manufacturing
processes over the 30-year period is what caused the
plant to be contaminated with PCBs?
A. I don't know that we've identified any other
reason.
Q. Okay. Did that answer my question? Are you
less than 100 percent certain that you are the source?
A. I guess the answer is I don't know that I
needed to be 100 percent certain in that case.
There
was enough certainty for us to move forward and to act,
and we did.
Q. In that case, there was enough certainty to
fairly establish that Monsanto was the source of PCBs
on its own property, correct?
A. I believe so.
Q. Now, during this process that you-all engaged
in in cleaning up your own property and the neighboring
properties, did you identify any other potential
sources of PCB contamination in the area?
A. I know that there were some issues on some of
the related property with PCB contamination that could
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have come from, I think, a prior -- I forget if it was
a -- some sort of a metal operation, but yes, there
were other users of PCBs in the area that could have
contributed materials to the property.
Q. But all of those other users got their PCBs
from Monsanto, correct?
A. I don't know.
Q. You don't know that even though on Exhibit No.
2 Monsanto has admitted that they are the sole United
States manufacturer of PCBs?
A. I think you're asking a different question,
because there were other people that sold PCBs, as I
understand it, from outside the U.S.
So there were
other manufacturers.
I don't have the records.
I
don't know where they would have come from or not.
Q. Under the Monsanto guidelines where we're
reading from on the corrective and remedial action
section, the section dealing with when Monsanto's
responsibility for cleanup is fairly -- excuse me, when
Monsanto's responsibility for contamination is fairly
established, it will take a leadership role in cleaning
up, that is the policy that Solutia employs today also,
isn't it?
A. I think the words say yes, that we're
following the words that you've identified.
I think
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they're somewhat different than what you paraphrased in
your statement.
I mean, I think it says we'll take a
leadership role in the process in moving it along.
Q. And Solutia does that also?
A. Yes.
Q. All right. Now, Mr. Pierle, do you believe
that Monsanto was fairly established to be the source
of the PCB contamination in that part of Snow Creek
that you-all removed some of the sediment to try to
remediate that portion of the creek back in the late
1980s?
A. Again, I don't recall, you know, the specifics
of that case. Certainly there was enough information
there and the judgment made to proceed and take
responsibility for that and to move on.
I don't know
what the factual basis around that was.
Q. But there was enough information there to at
least let Monsanto determine that it was "a" major
contributor, not necessarily "the," but at least "a"
major contributor in the PCB contamination on Snow
Creek that was somewhat remediated, correct?
A. I don't want to be argumentative about this.
I think what I'm saying is that if the judgment around
what you described was a couple hundred thousand
dollars to do the remediation and the work, that there
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was probably a sense that we could have been, we ought
to be part of this process, let's just get it done and
move beyond it.
I do not know in that context how much
was done about factually, Is it yours, is it somebody
else's, could they have come from someplace else.
I
just don't know how much of that was done.
Q. Before we broke for lunch, I asked you what it
would take to convince you that Monsanto was a fairly
established source of potential contamination in a
given situation. Do you recall that question or one
similar to that?
A. Probably.
Q. Do you recall telling me, sir, that if you
were presented with facts that demonstrated that
materials manufactured in Monsanto were present on-site
at a particular location and that the chemicals were
attributable to Monsanto's actions, then in your mind
that would fairly establish that Monsanto in that
situation would be a source of the contaminant?
A. I recall us writing down three sets of
assumptions of which I think you've talked about two.
So I don't know if you're asking me the same question
or a different question than what we responded to
before. Q. I thought I wrote your testimony down, and
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correct me if I'm wrong, that you said if someone presents a set of facts that Monsanto manufactured materials or discovered them being there as a result of actions that can be attributed to the company, then in your mind it is fairly established that Monsanto was a contributing source of the contamination; is that not a correct statement?
A. I think what I said at that point, that would be sufficient information for us to get involved in the process and to more fully understand the factual situation around that.
(PIERLE EXHIBIT NO. 8 WAS FIRST DULY MARKED, RECEIVED AND MADE A PART OF THE RECORD.) BY MR. GRAMMAS:
Q. I'm going to show you -- first of all, before I show you this, do you know who Mr. H.S. Bergen, Jr., is?
A. I'm vaguely familiar with the name. Q. Who is he? A. You know, I don't remember much more than Howard "BER gun", or "BER zhun" , seemed to be involved with one of the businesses some time ago, but I don't really recall. Q. Do you know who John Mason is? A. What is the middle initial?
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Q. Doesn't have one. It just says "John Mason."
A. There's been more than one John Mason, I
think, at Monsanto; although I'm not sure.
I know a
John Mason.
Q. Who is he, the one that you know?
A. The one that I know is the head of the
Monsanto Fund. He's at Monsanto.
Q. What is the Monsanto Fund?
A. A philanthropic fund operated by a board of
directors and president that disburses basically
contributions that the company makes to the fund, and
the fund makes judgments about, on a philanthropic
basis, where to deploy the funds.
Q. Does it ever deploy them for any environmental
issues, cleanups, stuff like that?
A. No. For cost of cleanup and things like that,
no .
Q. Mr. E.P. Wheeler, do you know who he is?
A. I believe he was a member of the corporate
medical department back in the late '60s, something
like that.
Q. How about Mr. Papageorge?
A. I know Mr. Papageorge. I worked for him back
in the '70s and he worked for me for a while in the
' 80s .
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Q. What did he do for you in the '80s?
A. I think he was part of -- at the time, was
part of the chemical company's organization when we
formed in '86, and I believe at the time he was dealing
with safety and industrial hygiene kinds of issues for
us .
Q. PCBs ?
A. I don't think so, I mean, not for what he was
doing for me.
I wasn't doing anything with PCBs.
It
was basically for safety and health programs across the
chemical company of Monsanto.
Q. F.J. Holzapfel?
A. Holzapfel.
Q. H-O-L-Z-A-P-F-E-L.
A. Right.
Q. Who's that ?
A. I knew Mr. Holzapfel when I was at a plant, I
guess, in New Jersey. He was the director of
manufacturing, I believe.
Q. What did he have to do with PCBs?
A. I have no idea.
Q. How about Mr. D.B. Hosmer?
A. Mr. Hosmer was a technical manager for a while
and was also a manager of an environmental and
utilities group in, I believe, industrial chemicals -
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well, he was when I came back from the government in
1975. He was my immediate supervisor at the time.
Q. What, to your knowledge, does he have to do
with PCBs for Monsanto? ,
A. At that time we were sort of getting out of
manufacturing, but he was, in general, at a company
level, responsible for environmental matters.
I don't
know what his specific -- I mean, he had people working
with him that were dealing with more specific matters.
Q. How about Mr. J.R. Savage?
A. I know Mr. Savage. He was sort of a technical
director and a licensing manager at a point in time.
Q. What did he have to do with PCBs?
A. I'm not certain.
Q. How about Mr. G.L. Jessee?
A. Well, I knew Gene when he was in the
environmental group that I was in in the corporate
structure in the mid-'80s.
Q. What did he have to do with PCBs?
A. I don't know. He was a former plant manager
at Anniston.
Q. Was he the plant manager in and around August
1970, to your knowledge? A. I don't believe so. I'm not certain.
Q. How about Mr. J.C. Landwehr, L-A-N-D-W-E-H-R?
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A. I'm not familiar with that name.
Q. How about Mr. Paul Hodges, have we talked about him before?
A. Paul was, I think, an environmental manager
that worked for Mr. Hosmer --
Q. Do you know - -
A. -- at one point in time.
Q. Do you know why all of the individuals that we
just talked about would receive a letter from Mr.
Hodges regarding a PCB cleanup program at Anniston? Do
you know why those individuals would have been selected
to receive such a letter?
A. I really don't.
Q. Is it Solutia's policy, and was it Monsanto's
policy, to fully disclose to the public any and all
impacts that its manufacturing processes and disposal
processes of its chemicals would have on the public or,
in particular, people that lived downstream from one of
its plants?
MR. PECK: Object to the form of the question.
THE WITNESS:
I really don't -- at what time
period?
BY MR. GRAMMAS:
Q. At any time period.
A. We have that as an explicit part of the policy
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and pretty much had since the mid '80s, I believe.
I
don't know -- I don't know that there was anything written or what the practice was before then. My own
experience was that most of those conversations would
typically happen with regulatory agencies who were the
representatives of the public, and that's typically
where most of the discussions that -- that was a
more -- more the practice back before the '84 time
period, as I recall.
Q. Can you think of any legitimate reason why
Monsanto would deliberately try to conceal information
it was aware of regarding PCB contamination of Snow
Creek, Choccolocco Creek, and fish contained in those
bodies of water from the people who live on those water
systems?
MR. PECK: Object to the form of the question.
THE WITNESS: No.
BY MR. GRAMMAS:
Q. Would it offend you, sir, to know that in
1970, Monsanto in fact embarked on a course of conduct
to deliberately conceal information it had discovered
regarding PCB contamination and Snow Creek, Choccolocco
Creek, and fish therein? MR. PECK: Object to the form of the question.
THE WITNESS: It would if that were true.
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BY MR. GRAMMAS:
Q. Can you think of any legitimate reason why a
company would want to keep confidential information
that it discovered regarding the amount of PCBs it was
discharging into Snow Creek on a given day; and not
only keep that information confidential within the
company, but to destroy the information once the
recipients of the information received the document
describing the amounts?
A. I mean, it's conceivable that at a point in
time, depending on where folks were with conversations
and with outside regulatory folks, what they may have
judged to be appropriate.
I'd have to understand more
about the facts to be able to respond any more to that
question, and then I'm not sure I could.
Q. Okay. I'm going to show you what has been
marked as Plaintiff's Exhibit 8 and draw your attention
to the first highlighted paragraph under the section
entitled "Status." Do you see that, sir?
MR. PECK: You're free to read the entire
document.
THE WITNESS: I do see that statement.
BY MR. GRAMMAS:
Q. If you'd like to read the entire document, you
can.
I'm going to ask you questions about this
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statement right here, though. Could you read that statement, please, out
loud. A. The entire -Q. First of all, this is a Monsanto document
dated August 7, 1970, correct? A. Yes. Q. And it's written to Mr. H.S. Bergen,
B-E-R-G-E-N, Jr., correct? A. Yes. Q. And the people that we were discussing moments
ago are all listed as recipients of the letter, right? A. Yes. Q. And who wrote the letter, sir? If you can
turn to the last page -- or, actually it's a memo. It's an internal memorandum.
A. It looks like a Mr. Paul B. Hodges. Q. And that's the same gentleman we talked about earlier, right? A. Yes. Q. And in the top of the memo, in bold and underlined for importance, is the words -- and actually, all capitalized, in the words "Confidential," right? A. Yes.
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Q. And then it says capital F, capital Y, capital
I. What does that mean? A. I assume it's "for your information."
Q. And then after that it says what, sir?
A. "And destroy."
Q. So we've got a document written by Mr. Hodges
to these individuals that said that this is
confidential and this is strictly for your information
and after you read it, destroy it, right?
A. Uh-huh, yes.
Q. Now, under the heading entitled "Status," it says what, sir, that's highlighted?
A. Well, highlighted in yellow is the first
sentence:
"We're presently discharging to Snow Creek
about 16 pounds per day of PCBs, down from 250 pounds
per day in 1969."
Q. Okay. So we know, as of August 7, 1970,
Monsanto had decreased from 250 pounds a day, the year
earlier, discharging 16 pounds every day of PCBs into
Snow Creek, right?
A. That's what this statement says.
Q. You don't have any reason to doubt the
veracity of that statement, do you?
MR. PECK:
Object to the form of the question.
THE WITNESS:
I guess I would really want to
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make sure I read the whole one to make sure that there
were weren't any other qualifications.
BY MR. GRAMMAS:
Q. I understand, but as that statement appears,
you have no reason, sitting here today, to doubt that
it's true, correct?
A. Not having read only that statement.
Q. As a matter of fact, sir, as the head of
environmental affairs, charged with the responsibility
of remediating this project here in Anniston with
respect to PCBs, this is the exact type of document you
would expect to read in determining what type of PCBs
may have been put into Snow Creek in the past that
Monsanto is responsible for, right?
A. I wouldn't personally expect to necessarily
read this, no.
Q. But somebody under your responsibility, if you
directed to go out and find out how many pounds of PCBs
were put into Snow Creek by Monsanto over the years,
would go to documents like this and read it and rely on
it, right?
MR. PECK:
Object to the form of the question.
THE WITNESS:
It could be one source of
information, sure.
BY MR. GRAMMAS:
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Q. Now, in the third numbered paragraph in this
letter it says that:
"Joe Crockett, secretary of the
Alabama Water Improvement Commission, will try to
handle this problem quietly without release of the
information to the public at this time."
Did I read that correctly?
A. Yes. Q. Now, if you would, sir, turn to the very last
page of the letter.
MR. PECK:
You know, Mr. Pierle, he's taking
you all through the letter, different things he wants you to read, and has asked you about pieces from it.
Feel free to read the entire thing.
BY MR. GRAMMAS: Q. If you want to read the entire letter, you're
more than welcome to.
MR. PECK:
Thank you.
BY MR. GRAMMAS: Q. Let me know when you're finished.
(WITNESS REVIEWS DOCUMENT.)
(A SHORT BREAK WAS HELD.)
THE WITNESS:
I have read it.
BY MR. GRAMMAS: Q. Okay, sir. After having now the benefit of
reading the entire document, is there anything that we
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have discussed about the internal memorandum at this
point that is not 100 percent true?
MR. PECK:
Object to the form of the question.
No foundation.
THE WITNESS:
I really don't have the basis
to -- you know, to answer that.
I mean, my assumption
would be that it's true.
BY MR. GRAMMAS: Q. And what I'm getting at more particularly is
the items about 16 pounds a day being discharged in
1970 versus 250 pounds a day of PCBs being discharged
into Snow Creek in 1969.
That statement that contained
at the beginning of the letter and nothing in the
remainder of the letter brings into question the
accuracy of it, does it?
A. Well, there's some further statements here
about overall accuracy of sampling and the methodology,
which indicates to me at least that they're looking at
the accuracy in their measuring devices to see whether
these are right.
But it doesn't go on to describe --
Q. And that's what they found based on their own
measuring devices, right?
A. Based on what methodology they were using at
that time. Q. And you have no reason to doubt that the
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methodology that they were using was accurate, do you?
MR. PECK:
Object to the form of the question.
BY MR. GRAMMAS:
Q.
I mean, you talk about methodology.
These are
documents produced by Monsanto, right?
A. Yes. Q. These are documents that Monsanto management was relying on in determining what, if anything, to do about the PCB problem in Anniston, right?
A. Yes. Q. And is there any reason to think that the information they were looking at was not accurate in making these decisions? A. I think they would have felt it was the best
that they had and as accurate as they could be. Q. And you couldn't make decisions based on the
PCB contamination problem with inaccurate information,
could you, or couldn't make the right decisions with inaccurate information, could you?
A. Again, my sense is it was probably as accurate
as it could be for what they were trying to do at that
time . Q. So based on this document in 1969 in Anniston,
you-all were losing about 250 pounds a day of PCBs into Snow Creek, right?
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A. What it says is at the time the document was
written, it was 16 pounds a day, and that that number
had represented an earlier period.
Q. No, what I was asking you about was in 1969,
this letter says that you-all were losing 250 pounds a
day.
A. That's the reference that's made in the
letter.
Q. And they were basically bragging about being
able to reduce those losses from 250 pounds a day to 16
pounds a day a year later, right?
A. I don't know if they were bragging. I think
what they're saying is factually they had been able to
do that, which represents, you know, a pretty good
reduction. Q. Okay. Now, do you think it's good policy,
sir, for a company to knowingly discharge 250 pounds of
chemicals a day into a river system that it knows was
toxic?
A. Again, now you raised a whole different
question, toxic and what concentration to whom and to
what.
So I don't think that this statement says that
they knew it was toxic in the stream or in the
conditions of Snow Creek.
Q. My question didn't ask you what your
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understanding of toxic was, sir.
My question to you
was simply:
Do you think that it was good practice for
a company to knowingly discharge 250 pounds of PCBs into Snow Creek a day in 1969 and, according to this
document, 16 pound of PCBs into Snow Creek in 1970,
when all along, while it was dumping those chemicals
into Snow Creek, it knew that the chemicals were toxic?
MR. PECK:
Object to the form of the question.
BY MR. GRAMMAS: Q. Do you think that's good practice? A. Again, I have to define "toxic" to be able to
answer that question, and I did, and I answered that it
was common practice for more pounds of that of
materials and chemicals to be discharged into rivers
and streams in the United States at that point in time,
which in generally was viewed as acceptable.
Q. And because -- when you say it's "common
practice," that meant not only Monsanto was doing it,
but other chemical manufacturers were dumping toxic
chemicals into the river systems, too, right?
A. And municipal treatment -- municipal systems
and discharges and commercial entities and basically
that was the norm of the day. Q. And because everybody else was doing it, it's
okay for Monsanto to do it; is that what I'm hearing
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you say?
A. I think what I'm saying is that was generally accepted practice based upon the information that one
knew at that point in time.
Q. Now, was it generally accepted practice that
these other chemical companies and cities and whoever
you're referring to generally, but not by name, who
were discharging -- are you saying that they too knew
that what they were discharging into their systems was
toxic or that they were just discharging without
knowledge at all?
A. What I'm saying is that people knew that there
were discharges going that contained materials that may
have hazardous properties.
I'm not saying that people
were knowingly discharging hazardous materials that had
toxic end-point conditions to the environment or to
human health.
Q. Who is Dr. R. Emmet Kelly?
A. Dr. Kelly was the medical director for
Monsanto Company for a period of time back in -- well,
I don't know when he started.
He was there when I was
there in the mid-'60s, it seemed like, to '70s,
somewhere in that time.
At least that's where I'm
familiar with the name. Q. Did you ever have an opportunity to work with
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him?
A. I think I met Dr. Kelly a time or two, but I
don't recall really any project work that I did with
him.
I recall he was pretty senior and I was pretty
j unior.
Q. Do you know what his reputation was within
Monsanto?
A. I really couldn't characterize that. I didn't
know him well enough or didn't know of him enough to
know of that.
I think subsequent to that, you know, I
think there's a general sense that he was a very good
doctor.
(PIERLE EXHIBIT NO. 9 WAS FIRST DULY
MARKED, RECEIVED AND MADE A PART OF THE RECORD.)
BY MR. GRAMMAS: Q. Mr. Pierle, I'm going to show you what's been
marked as Exhibit 9 to your deposition, and ask if this
is not a letter dated September 20, 1955, to Dr. J.W.
Barrett from Dr. Kelly? You can look at the second
page for his signature.
MR. PECK:
And again, he's going to talk to
you about the letter.
Feel free to read it.
THE WITNESS:
It is a letter from Dr. Kelly
to -- it looks like a J.W. Barrett, yes.
BY MR. GRAMMAS:
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Q. And J.W. Barrett has the word "doctor" before his name, too, doesn't it?
A. It does. I don't know what that means.
Q. The subject of this letter is Dr. Barrett's September 8 letter to Mr. -- it looks like Mason, about
Aroclor toxicity, correct?
MR. PECK:
He's going to ask you about the
subject of the letter, and you're going to have to read
the letter.
THE WITNESS:
I will.
BY MR. GRAMMAS: Q. Isn't that what the subject says at the top,
sir?
A. Yes. Q. Aroclor is a company name for PCB, right?
A. Can I read the letter?
Q. You can read the letter, sure. (WITNESS REVIEWS DOCUMENT.)
THE WITNESS:
I have read the letter.
BY MR. GRAMMAS: Q. Now, Mr. Pierle, I want to draw your attention
to the last paragraph on the first page.
MCC, what is
MCC, Monsanto Chemical Company?
A. It probably is. Q. Doesn't Dr. Kelly tell Dr. Barrett that
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Monsanto Chemical Company's position about PCBs can be summarized in the following fashion, and see if I read
this correctly.
"We know Aroclor" -- first of all,
Aroclors are PCBs, right?
A. Again, I think they can be. I'm not 100
percent conversant on the product terminology that was used.
Q. Well, assume for me that Aroclors are PCBs,
okay, because that's been the testimony in the past.
MR. PECK:
Object to the form of the question.
I'm not sure that that's an accurate characterization. I think the testimony's been that Aroclor includes
PCBs.
It's not necessarily all PCBs.
MR. GRAMMAS:
Well, we'll take that
definition.
BY MR. GRAMMAS: Q. Monsanto Chemical Company's position can be
summarized in the following fashion.
"We know Aroclors
are toxic, but the exact limit has not been precisely
defined." Did I read that correctly?
A. Yes.
Q. Dr. Kelly goes on to state:
"It does not make
too much difference, it seems to me, because our main
worry is what will happen if an individual develops any
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type of liver disease and gives a history of Aroclor
exposure.
I'm sure the juries would not pay a great
deal of attention to MCC's position."
Did I read that correctly?
A. I think you did, up until the last word, and I
think that refers to MACs, attention to MACs, and I
think that's used someplace else in here.
Q. Yeah, I think you're right.
I misread that.
In any event, Dr. Kelly, back in 1955, wrote
to Dr. Barrett, who was another Monsanto doctor, that
Monsanto doctors on staff knew that PCBs were toxic to
human beings, didn't they?
A. No. Q. Okay. And he didn't also write that he's
worried that exposure of individuals to Aroclors may
cause liver disease.
He didn't write that either, did
he?
A. That's not how I interpret what he says. What
I interpret what he says here is that -- and I don't
know that Dr. Barrett is Monsanto.
So, again, I'm not
agreeing to your front end.
I just don't know.
You
made that factual statement.
Q. I just assumed he was. Dr. Kelly wrote a
letter to an individual.
Regardless of whether that
individual's employed by Monsanto, you will admit that
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Dr. Kelly was employed by Monsanto?
A. Yes. Q. And he wrote a letter to this man stating in
1955 that Monsanto Chemical Company knew that Aroclors
were toxic.
A. I think what this is saying is that based on
some tox test that was available, I think he describes
up above that Aroclors are toxic.
Almost everything's
toxic.
So there's nothing new about that.
The
question here, as I read this, is:
At what level is
there toxicity? And what he goes on to say, as I read
that, it says what's important here is that we
understand if there is any liver disease in humans and
is there Aroclor exposure that may have contributed to
that.
So this doesn't say that he is stating that
Aroclor causes liver disease, he is simply stating that
I don't know whether there's a reason to do more
toxicological studies on animals or how valuable that
would be.
Q. Well, he says Monsanto knows that Aroclors are
toxic, but the actual limit has not been precisely
defined.
A. Right. That's correct. And most toxicity is
done in animals, and my interpretation of that is it's a question of at what level is toxicity exhibited in
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the animal.
Q. And, of course, you're going to point me to a
study that Monsanto has that says, We know discharging
250 pounds of this toxic chemical a day does not rise
to that level of toxicity that Dr. Kelly was concerned
about.
Where's that document?
MR. PECK:
Object to the form of the question.
THE WITNESS:
I didn't -- I didn't suggest
that there was a document, if you state it in fact.
BY MR. GRAMMAS:
Q. Exactly. So the best you can tell me is, in
1955, Monsanto knew that it was discharging a toxic
chemical -- scratch that.
In 1969, Monsanto knew that it was
discharging, according to Plaintiff's Exhibit 8 to your
deposition, 250 pounds of this toxic chemical a day
into Snow Creek, right?
A. That's what the one document suggests.
Q. Well, the two documents together prove that
Monsanto knew they were discharging a toxic chemical of
up to 250 pounds a day into Snow Creek, right?
A. No. I mean, what it says is we're
discharging -- it's two separate things.
One, we're
discharging up to or were, which has been reduced; and
Aroclors exhibit toxic properties in test animals.
And
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what it goes on to say, as I read it, that is
questioning down here further as to what's important,
is:
Are we seeing any adverse effects in human beings
and are there any actual exposures to PCBs which may
cause that effect?
Q. Mr. - -
A. The presence of the material and the fact that
a material has toxicity does not allow one to conclude
that there's any risk to the environment or an
individual as a result of that.
Q. I didn't ask you any of those things, Mr. Pierle, and I appreciate your contributing all of that
unnecessary information, but that's not what I asked
you.
My questions are very simple, they're very
pointed, and I want answers just to those questions and
we can get out of here a lot faster.
MR. PECK: Mr. Pierle can answer the question
however he feels fit.
BY MR. GRAMMAS: Q. When you do that, it makes me come back and
show that the witnesses in these letters did not say
the things you just said.
So that's what we're going
to do here.
In this 1955 letter, Mr. Pierle, Dr. Kelly is
not talking about rats.
He's talking about human
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beings, isn't he? You've already read the whole
letter.
A. No, he is not saying that they have determined
that Aroclors were tested on human beings and toxic to
human beings.
The letter does not say that.
Q. He did not mention the word "rats," "animals,"
"mice," "dogs," "puppies," "gerbils," anything of that
sort in this 1955 letter, did he?
A. Well, let me look at it again, but he did not
say that they were -- it refers to test work that was
done; and the best I know, it was not common practice
to test human beings directly for toxicity for
chemicals.
The standard practice was to test animals.
So maybe it doesn't say it specifically, but it's a
fairly simple deduction for someone to make from this
discussion.
Q.
I'm not asking you to deduce anything.
And if
your lawyer wants to talk to you about that, that's
fine .
MR. PECK:
Sure, you are.
You're asking him
to deduce things.
You're asking about documents.
If
you don't want to know his interpretation of the
document, stop showing him the document.
MR. GRAMMAS:
If your lawyer wants to ask you
questions about why you feel like something should have
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been written in that letter that wasn't, then he can
have every opportunity to do that.
What I'm asking -
MR. PECK:
You asked him -- you had asked him
if the letter said toxicity to humans, Pete.
MR. GRAMMAS:
Adam, be quiet.
I know what I'm
asking.
MR. PECK:
Well, you apparently don't, because
you're getting answers to your questions and you don't
like them and you don't know what the answer means.
MR. GRAMMAS:
Whatever, Adam.
MR. PECK: And that's why you have to keep
asking him the same questions
MR. GRAMMAS: Whatever.
MR. PECK:
Listen to his answers, Pete, and
stop asking him the same questions over and over again.
BY MR. GRAMMAS:
Q. Can you answer the question, sir.
MR. PECK:
Read back his answer.
BY MR. GRAMMAS: Q. There's nothing in there about rats, mice,
animals, gerbils, dogs, puppies, cats, anything, is
there? A. My interpretation of MAC is "maximum allowable
concentrations."
That is a term that is very commonly
used around the testing of laboratory animals.
So
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again, someone with some understanding of scientific testing -- and I'm not an expert -- would sure assume
and deduce from this letter that's exactly what they're
talking about.
Q. That would have been a perfect answer if I
asked you to assume and deduce for me what they're
talking about.
But my question was:
Do those words
appear in this letter anywhere, about animal studies,
dogs, rats, mice, gerbils, anything like that?
Do they
appear in this letter, sir?
A. Again, MACS would interpret that, and nothing in the letter says it's talking about human toxicity
testing either. Q. Fine. Where were you in 1955?
A. I was born - MR. PECK: Now he is trying to disqualify him.
BY MR. GRAMMAS: Q. What were you doing in 1955?
A. I was 12 years old, so I was probably in grade
school. Q. What grade would you have been in?
A. Is this relevant? Q. Uh-huh. Yes, sir. A. I was probably in the seventh grade.
Q. You were in the seventh grade. You were a
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12-year-old boy when Dr. Kelly wrote this letter.
A. That's correct. Q. And he states in here that Monsanto Chemical Company's position -- not Dr. Kelly's, he said this is
the chemical company's position -- is that they know
Aroclors are toxic.
A. That's correct.
Q. Now, and we've know that from 1955 . A. Yes . Q. What's the date of Exhibit No . 8, sir?
A. August 7, 1970. Q. Now, according to Exhibit No. 8, which is a Monsanto document, how many pounds of PCBs were being dumped into Snow Creek in 1969 on a daily basis?
A. This suggests their best information says it's
250 pounds a day. Q. Simple question. Based on these two documents
together, can you not tell me that Monsanto was dumping
250 pounds a day of a toxic chemical into Snow Creek?
MR. PECK:
Object to the form of the question.
THE WITNESS:
No.
BY MR. GRAMMAS: Q. Back to Exhibit No. 8, sir, which is the Paul
Hodges letter dated August 7, 1970, he discusses in the
last paragraph of his letter that high concentrations
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of PCBs were being found in mud and fish in Choccolocco Creek, doesn't he?
A. He says: "...fish samples from nearby Choccolocco creek also showed high levels of PCBs, we're instituting more sampling to determine the extent of the problem."
Q. Right. Back in 1970 -- where in that letter, by the way, does he say. But Monsanto's not the party responsible for the high levels of PCBs in these fish?
A. I don't think he discusses responsibility at all.
Q. Where in there does he say that Monsanto is not responsible for doing it?
A. I didn't say that he said that. Q. I know. I'm asking you where is it that he says that, if he does? A. I don't know why he wrote the letter and what he put in the letter, whether that was even pertinent. Q. Would you not say that, reading that letter, it's a fair conclusion to take from it, sir, that Mr. Paul Hodges believed that Monsanto was the party responsible for the high levels of PCBs in the fish found in Choccolocco Creek? A. I think what they're doing there again, as I read that letter, is looking at facts and information.
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Certainly there was enough that caused him to go look
and ask the question and they were also disclosing that and discussing with the state officials.
Q. At the same time, they were making sure that the public didn't get a copy of this and didn't find
out this information, right?
A. That's what this letter says. I don't know
how many other letters or what else was produced.
This
doesn't say that they wouldn't give it to the public.
It just says with respect to this letter, it's
confidential.
Q. What's the date of that letter?
A. August 7, 1970. Q. Who's Mr. G.W. Miller?
A. I don't know.
(PIERLE EXHIBIT NO. 10 WAS FIRST DULY
MARKED, RECEIVED AND MADE A PART OF THE RECORD.)
BY MR. GRAMMAS: Q. Well, I'm going to show you a letter dated May
7, 1970, sir, and I ask if you would, please, review
that letter.
I want to ask you a few questions about
it .
(WITNESS REVIEWS DOCUMENT.)
BY MR. GRAMMAS: Q. Have you had an opportunity to read Mr.
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Miller's letter to Mr. Jessee?
A. Yes.
Q. It's actually an internal memorandum, as opposed to a letter, but it's dated May 7, 1970,
correct?
A. Yes.
Q. And it deals with the subject of Monsanto
putting PCBs from its Anniston plant into Snow Creek
and Choccolocco Creek, doesn't it?
A. I don't think it mentions Choccolocco Creek.
Q. Just Snow Creek?
A. I believe that's what the letter says.
Q. All right. Under the third full paragraph,
there are some topics of discussion, correct?
A. Yes. Q. And Mr. Miller is telling Mr. Jessee that
Monsanto has made the decision to "Give no statements
or publications which would bring the PCB contamination
to Snow Creek's situation to the public's attention."
Isn't that what he says?
A. This says his recommendation, "his" referring,
I believe, to Mr. Crockett.
So these were the
recommendations of the Alabama state administrator to
do that.
And he goes on to say:
"If approached,"
people are free to discuss the situation and that it's
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under study and Mr. Crockett -- under his direction.
Q. All right. Maybe you didn't understand my
question.
He states in here that Monsanto is going to
take the position that it will "Give no statements or publications which would bring the situation to the
public's attention."
Did I read that correctly?
MR. PECK:
He answered your question, Pete.
If you didn't like the answer, then stop asking him
questions.
BY MR. GRAMMAS: Q. Did I read it correctly?
A. Again, what that says is his recommendations,
the way I read that, that Mr. -- those were Mr.
Crockett's statements and recommendations.
Those were
not the statements of Mr. Miller.
Q. What's AWIC?
A. I believe it's the regulatory authority in Alabama at that time.
Q. Let's read this paragraph above that section
for a moment.
Paragraph 3 of the letter says:
"Mr.
Crockett was most appreciative of Monsanto's approach
to the problem and the fact that Monsanto came to him.
Did I read that sentence correctly?
A. Yes.
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Q. And the problem, again, is PCB contamination from Monsanto's plant into Snow Creek, right?
A. I think it's a variety of information that had been discovered concerning PCBs, the plant site, and
Snow Creek.
Q. "He," being Mr. Crockett, "alluded that our
action" -- that's Monsanto, right?
A. Yes. Q. -- "would produce a situation that was
beneficial to the protection of both the Monsanto and
AWIC positions."
Correct ?
A. Yes. Q. "His recommendations were as follows," and
then it says:
"Give no statements or publications
which would bring this situation to the public's
attention."
Did I read any of that incorrectly?
A. No, you did not.
Q. Now, tying it back to the words of Mr. Miller, would not "giving no statements or publications to the
public" protect Monsanto's position with respect to
PCBs being dumped into Snow Creek at that period of
time, sir? A. That is not the way I read the letter.
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Q. Okay. Have you ever been aware of the fact that free globules of Aroclors had been seen in Snow
Creek from Monsanto's plant?
A. I don't believe so. Q. Would that surprise you to know that?
A. If those levels of discharge were accurate,
that would be possible.
Q. Do you think that's good corporate practice, even back in 1969, to dump so much PCB into Snow Creek
that free-standing -- what was the word they used? - "free globules" of the stuff can be seen in the creek?
A. You know, again, by today's standards, we
wouldn't do that, we couldn't do that.
By the
standards that existed at that point in time, that was not uncommon practice.
Q. But -A. Folks knew about it, the public knew about it.
It was accepted.
Things changed and the laws changed
and there was a whole structure put in place to deal
with that, but that was accepted behavior and practice at that time.
Q. The public knew about it.
Is that what I
heard you say? A. What I'm saying to you in general, the
question of discharges of pollutants in the rivers and
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streams at that time was public knowledge, generally
available.
People knew there was pollution at that
point in time.
People knew and regulators knew there
were things that floated on streams and sank to the
bottom.
So, you know, anyone at that point in time
would have known that that was not uncommon.
Q. Including the people at Monsanto?
A. I think everybody pretty much was aware of
that.
Q. Now, does the fact that there were free
globules or Aroclors found in Snow Creek, the fact that
there were 250 pounds a day of PCBs being discharged
from your plant directly into Snow Creek, influence in
any manner whatsoever your opinion that Monsanto is a
potentially responsible party or the responsible party
for the problem that we're seeing in the creek and the
lake today?
A. I think, again, we've talked about this. With
respect to what was in Snow Creek, that situation, it
has been addressed and is being addressed.
With
respect to Choccolocco Creek and the lake, there's
significant studies which we are leading, participating
in, that are getting additional answers to that
particular question.
And the reason why we're there
doing that is because there's enough information that
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says, by our policies and guidelines, we ought to be in the process of understanding what's there.
Q. And we had that information, sir, as early - "we" being you -- had that information as early as May 12, 1969, didn't you?
A. They had information relative to Snow Creek and it was disclosed and discussed with the regulatory authorities.
Q. Well, let's look at -- Exhibit 8 is dated August 7, 1970, and it's talking about fish samples in Choccolocco Creek, isn't it?
A. It does. Q. So Monsanto had information in the '69 time period that its manufacturing process and discharges of PCBs were impacting Snow Creek and Choccolocco Creek, right? A. I think it says there were PCBs there. This does not say that that plant was the source or only source of that material.
(PIERLE EXHIBIT NO. 11 WAS FIRST DULY MARKED, RECEIVED AND MADE A PART OF THE RECORD.) BY MR. GRAMMAS:
Q. All right. Sir, I'm going to show you what has been marked as Plaintiff's Exhibit 11 and ask if you can identify that for me just by looking at the
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date, the author, and the recipients? A. How do you want me to identify this? Q. By telling me who wrote it, what it is, and
what -- the date it was written, and who got it. A. It's a letter from Mr. Hodges to a Mr. Kuhn
dated May 12, 1969, subject, "Aroclor Cleanup from Plant effluents.
MR. PECK:
He's going to ask you questions
about the document, Mike, you'll have to read it.
BY MR. GRAMMAS: Q. Heading 3 of this document says: "Work to
Minimize Losses at Anniston."
Did I read that correctly?
MR. PECK: He's going to ask you questions about the document, Mike, you need to read it.
BY MR. GRAMMAS:
Q. Read that whole document.
I'm going to run to
the restroom.
MR. GRAMMAS :
Adam, we'll be here all day
reading these.
MR. PECK:
That's f ine .
That's your choice.
MR. GRAMMAS :
All right.
Well, just so this
gentleman knows that the reason he's here all day is
because you're making him read letters.
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MR. LOWE:
That's okay.
(WITNESS REVIEWS DOCUMENT.)
(A SHORT BREAK WAS HELD.)
THE WITNESS:
I have read the document.
BY MR. GRAMMAS:
Q. Now, let's turn our attention to Roman -
Section Roman numeral III, it's "Work to Minimize
Losses at Anniston," right?
A. Yes. Q. And they define the problem, do they not, in this document; does Monsanto not define the problem? A. That's a heading that's used. Q. And the definition of the problem is that:
"External to the plant -- that a problem exists at Anniston is evident because 'free' globules of Aroclors can be seen in Snow Creek."
Did I read that correctly?
A. Yes. Q. "We do not know what problem exists in
Choccolocco Creek and the Coosa River."
Did I read that correctly?
A. Yes.
Q. Now, it says:
"Two sets of mud and water
samples will be taken in Choccolocco Creek."
Right?
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A. That's what it describes. Q. Okay. Now, we know -- well, that was May 12, 1969, right? A. Yes. Q. And we know, as of August 7, 1970, those samples were taken by Monsanto at Choccolocco Creek, right ?
A couple months later, we have the results of the fish samples that we talked about in the prior document, Exhibit No. 11.
A. Well, I mean, it's over a year between the two documents, so I'm not sure if they're talking the same samples or not.
Q. But you will admit that there are samples from Choccolocco Creek that show positive readings of PCBs in the fish there?
A. Yes. Q. Okay. Now, on another section here, entitled "Internal Plant Problems," on the following page, paragraph 2 e., states that Monsanto should "Establish continuous monitoring stations on Choccolocco Creek for Aroclors (and PNP and Parathion)."
Did I read that correctly? A. Yes. Q. What does EDC mean?
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A. I think it's "estimated date of completion."
Q. June 1st, 1970, right?
A. Yes. Q. Tell me how many monitoring stations Monsanto
has on Choccolocco Creek right now, sir, checking for
PCBs . A. I don't know that we have any.
Q. Is it safe to say that it's now, what, 28
years later, you didn't -- Monsanto didn't meet their
estimated date of completion for putting those
monitoring stations in to check the PCB contamination
in Choccolocco Creek?
A. No .
MR. PECK:
Object to the form of the question.
BY MR. GRAMMAS: Q. It's not, why not?
A. They were probably put in, work done, and
taken out.
That's relatively common practice when
you're doing monitoring and that.
Nothing in that
document says we're going to put them in and leave them
forever.
This was a document that describes the work
plan aimed at definition of problems --
Q. So - A. -- of a project. Q. So you know for a fact, as the environmental
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manager for Solutia, that as of 1970, Monsanto had installed monitoring stations in Choccolocco Creek to
check for PCBs?
A. I didn't say that.
Q. Well, you said that they probably did them and
took them out.
A. You asked me a different question as to
whether or not they existed today.
My response was the
fact that they said that they would put them in doesn't
mean if they did, they would be in existence today.
Q. And the fact that they said that they should
put them .in doesn't mean that they did, either, does
it?
A. I don't know whether they did or not. From
that note, I can't tell.
Q. Monsanto employees back in 1969 thought it was
important enough to put PCB monitoring stations in
Choccolocco Creek; you will agree with me at least as
to that, based on this document?
A. It says it was part of that comprehensive work
plan.
Q. And isn't that because as early as that date, y'all knew that your PCBs were getting into Choccolocco
Creek and you just wanted to know how much?
A. I think what that whole program describes is
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an investigatory set of work that was undertaken at
that point in time to understand losses at the plant and where they might be going.
Q. And back then they thought they were going as far as Choccolocco Creek, didn't they. May 12, 1969?
A. I think what that suggests is they wanted to
check and see if that was the case or not.
It doesn't
assume that they knew that they would.
Q. But we know now in hindsight that the PCBs were in fact getting into Choccolocco Creek, don't we?
A. I think that one date says that there are
PCBs.
It doesn't say where they're from and it says
that they're there; and as a matter of fact, there were
subsequent actions, I think, by the State on that at a
point in time.
I don't know when it was, but again,
this is open -- I believe, open knowledge.
Q. But it's not open because of anything that Monsanto chose to disclose to the public, is it?
A. Absolutely, because if you choose to disclose
it to the regulatory agency who is the public.
Q. Okay. And the fact that you-all say on
August 7, 1970, that this is confidential information,
that once the recipients read it, they should destroy the letter, and that they should try to handle the
problem without releasing the information to the
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public, doesn't affect, in your mind, or doesn't draw
you to conclude that Monsanto's doing everything in its power to conceal this problem from the public?
A. I think what all of that suggests is there was
open communication to the state agencies and the State
was well aware of it and the State basically said,
We're working on this together, there's no need to
alarm the public with it.
And basically, though, if
asked, that people will tell there's a program underway
to investigate and understand the situation.
Q. And the fact that y'all were writing these
memos on August 7, 1970, saying, Let's keep this from the public, let's read this among ourselves and then destroy this information, didn't have anything to do
with the fact that y'all were worried about the public
finding out and suing y'all over these issues; is that
what I'm hearing you saying?
MR. PECK:
Object to the form of the question.
THE WITNESS:
No, you're reading one letter in
'70 and you're showing me another letter that talked
about a conversation that wasn't marked that way that
would have been open and available.
So I don't derive
any special meaning from that designation.
BY MR. GRAMMAS: Q. Okay. Well, we'll go through it, then, in
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detail so we won't mislead anything or anyone.
Again, Mr. Paul Hodges' letter dated August 7,
1970, to Mr. Bergen, in bold, underscored, all capital
letters, says:
"Confidential, For Your Information and
Destroy." Did I read any of that incorrectly?
A. No. Q. And it says in the third paragraph of this letter that we're going to do everything we can to keep this from the public, right?
A. No. Q. Okay. What does it say?
A. It says exactly what it says.
Q. Read it.
A. Mr. Crockett "will try to handle the problem
quietly, without release of the information to the
public at this time.
He believes that FDA will not
precipitate this matter...Dr. Myers, Director of Public
Health... wants toxicity information on PCBs and will
convey this personally to him the next week.
That
clearly indicates to me there's an open flow of
information with state agencies, and I can't call that
confidential at that point.
Q. I didn't ask you what -- anything about a
state agency.
I'm talking about the people.
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A. You asked me to read the statement, and I did, and the state agencies are the ones that made the
statement that you attributed to Monsanto or Solutia, and I'm just pointing that out.
Q. Okay. Well, let me ask you this, then, Mr.
Pierle:
Monsanto, according to what I'm hearing you
say, never took the position that it personally wanted to keep this quiet from the public to avoid being sued
by someone; that was never a concern on your part?
A. I don't know what these people were thinking.
I'm talking to you about what's in this document at
this point in time.
Clearly there was an open
discussion with people at this -- outside of Monsanto,
of the information.
Q. There was no discussion of this with the
general public, was there, based on that letter, Exhibit No. 8?
A. I don't know at what point in time there was. Q. At this point in time, sir. A. It doesn't describe that it is, no. Q. As a matter of fact, it says don't tell the
public this stuff. A. I answered that question and that's not what
that says.
MR. PECK:
Let's take a break.
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(A SHORT BREAK WAS HELD.) BY MR. GRAMMAS:
Q. Mr. Pierle, are you testifying today that Monsanto, during this period of time, 1969/1970, when all these memos that we've been discussing came out, did not undertake to keep this quiet from the general public to avoid being sued by anyone with respect to the PCB losses that you-all knew were occurring in Anniston?
A. I can't conclude that from these documents. Q. You were employed with the company at this time, were you not? A. Yes. Q. You were working with some of these people, weren't you? A. To some extent, but not in detail. Q. And it never came to your attention, either at that period of time or during the course of your promotion within the company, and even today as the head environmental manager, that Monsanto tried to keep PCB losses a secret from the public so it wouldn't be sued? That was the real reason to keep it a secret, wasn't it? A. No.
Q. Did you say no?
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A. I'm saying no, it wasn't kept a secret, from
my reading of the documents.
(PIERLE EXHIBIT NOS. 12 AND 13 WAS FIRST DULY
MARKED, RECEIVED AND MADE A PART OF THE RECORD.)
BY MR. GRAMMAS:
Q. Toby Bell, who is that, do you have any idea?
A. I don't know.
Q. I'm going to show you a memo dated September
18, 1970, again from Mr. Paul Hodges.
Now, who did you
say that Mr. Hodges was and what did he do at that time
for Monsanto?
A. I think he was an environmental manager
working for Mr. Hosmer.
Q. September 1970, Mr. Hodges wrote Mr. Bell and
he told him in that letter that I've just handed you as
Plaintiff's Exhibit -- what is it, 13?
A. Yes .
Q. -- that Monsanto was extremely reluctant to
let the public know about any of these PCB lawsuits
because you were afraid you were going to be subpoenaed
and you were going to be sued, correct?
A. Can I read the letter?
Q. Yes, sir.
(WITNESS REVIEWS DOCUMENT.)
THE WITNESS:
I've read the letter.
Can you
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repeat the question.
BY MR. GRAMMAS:
Q. Yeah. You-all were concerned, deeply
concerned, about being sued during that period of time,
weren't you, based on that letter?
A. I think it says "from the legal standpoint,"
which again I would interpret to be, you know, the law
department's standpoint.
That's how I would interpret
that.
Q. Well, all lawsuits are legal in nature, aren't
they?
A. Yeah. That wasn't my response to it.
Q. I mean, that goes without saying.
A. There are legal departments, there are
management departments, and business people, and if you
were a lawyer inside Monsanto, I think you would
probably advise that, you know, this could be tough
from a legal standpoint.
I don't read that that's the
basis on that decision making -- that's one input into
this note.
That's how I read the memo.
Q. Well, rather than using your words to describe
this memo, don't you think it would be better to use
Mr. Hodges' words, the man who wrote the memo?
A. You're asking me to react to a memo, and I'm simply putting it in my context of understanding what
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my interpretation to be.
You would have to ask Mr.
Hodges, if you could, and you can't unfortunately.
Q. Has he passed away?
A. He has.
Q. Well, Mr. Hodges said, and I'll quote it and
you tell me if I'm reading it incorrectly:
"There is
extreme reluctance to report even the relatively low
emission figures because the information could be
subpoenaed and used against us in legal actions."
Did I read that correctly?
A. It started with "from a" -- "From the Legal
standpoint," and then you read it correctly.
It also
states in there we've got to give the data to the State
folks.
So they're going to give it to them anyway.
He
goes on to ask, then, what else can be done, even at
those low levels, to reduce them further.
Q. What it's saying is that Monsanto had hoped
that they would be able to improve what was happening
and demonstrate a favorable trend to the State, but
rather than being able to improve that, the emissions
had considerably increased based on the information
that they found; didn't he say that, sir?
A. Yeah, I think it's a disappointment that the
programs had not reduced it, and he goes on to say what
else can be done to reduce it.
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Q. And given the content of this letter, sir, is it still your testimony that Monsanto at that period of
time was not consciously concealing from the general
public the data that it was collecting to avoid being
sued by the people who were being affected by the
discharges that they were putting into Snow Creek and
Choccolocco Creek?
A. Again, I think there were at least three
questions in there.
Q. There was only one question.
A. Maybe you could shorten it and ask it to me
again.
MR. GRAMMAS:
Would you read it back to him.
(THE PREVIOUS QUESTION WAS READ BACK.) THE WITNESS: Again, I read that to be common.
What I said was that I don't believe that I see
anything in here that Monsanto was attempting to
intentionally keep matters from the public because of a concern about a lawsuit.
BY MR. GRAMMAS: Q. Despite the letters and the words and the
sentences contained in Mr. Hodges' September 18, 1970,
memo to Mr. Bell, which is Exhibit 13 to your
deposition?
A. Yes.
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Q. All right. I'm going to show you a fairly
lengthy document.
It's 12 pages.
If you want to read
it, you're free to read it.
I'm not going to ask you
about all 12 pages, I'm going to ask you about certain
sections.
Do you want to read the whole document or
not ? A. I think it has been important so I understand
the context in which the sentences are that you pull
out.
(WITNESS REVIEWS DOCUMENT.)
(A SHORT BREAK WAS HELD.)
BY MR. GRAMMAS: Q. Have you had an opportunity, sir, to read
Plaintiff's Exhibit 12?
A. Yes. Q. It's an October 2nd, 1969, memo regarding a
report from the Aroclor ad hoc committee, correct?
A. Yes. Q. And it's to Mr. Bergen and Springate. We
haven't talked about him.
Who's that?
A. I remember him as another business manager,
business director. Q. From Hodges and several other individuals,
right ?
A. Yes.
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Q. Can you identify the handwritten notes on this document, do you know who wrote them?
A. No. Q. All right. Do you believe that the toxicity of PCBs toward certain species is high?
A. I believe -- I think that's what the document refers to.
Q. Is that your understanding of the nature of PCBs as we sit here today?
A. I think it can be. There was some confusion that I'm not certain about with respect to wildlife as
to whether or not, you know, back at that time PCB was
the agent or DDT.
There was some confusion back then,
but I think kind of the assumption was all through this
that there is, you know, environmental toxicity that we
need to be concerned about.
Q. And you will agree with me that PCBs are a
very persistent chemical?
A. Yes. Q. And you will agree with me that the likelihood of natural -- it says "origin," what does that mean?
A. I don't know. Q. It says "or degradation," that makes more sense to me, but the "likelihood of natural... degradation of PCBs is remote."
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Do you agree with that? A. You know, I think at that time it was true. I'm less certain if we know any more about that today.
Q. And that's a fancy way of saying once the stuff gets into the environment, it ain't very likely
to go away on its own, right?
A. Yes. Q. All right. Now, under this section entitled
"Recommendations" in this same memo. Plaintiff's
Exhibit 12 to your deposition, the gentleman who wrote
this memo said that:
"In view of legal and moral
considerations," that Monsanto should notify all
Aroclor customers of environmental contamination
problems.
Did I read that correctly?
A. Yes. Q. All right. But it doesn't say anywhere in
here that Monsanto should notify all the people who
live downstream from its plant in Anniston who were
receiving PCBs being dumped into their river system
about the environmental contamination problem, does it?
A. It says what it says.
Q. You've read - A. You're presuming in your statement, at least to me, that there was knowledge and fact about that it
was -- you know, where there were exposures to human
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beings.
I don't read that in this document.
Like what
this is saying is our customers are buying this from
us, using this, we know to some extent what those uses
are and we ought to tell them what we know -- or, what
the current situation is about PCBs.
Obviously we
weren't hiding anything at that point.
Q. Well, you had a recommendation to tell your
customers, right? We can see that.
A. Right.
Q. Does it say anywhere in here a recommendation
to tell the people that lived downstream from your
plant about these same environmental problems?
A. No, it does not.
Q. And would you not believe that the people who
lived downstream from you are just as important, had
just as much right to know about environmental problems
as did your customers at that time?
A. As I read that memo and at that point in time,
it talks about understanding again what else we know
about the manufacturing facilities and where it is and
certain facts in there and a work plant around that,
and that was again in and around the time that the
agencies were known.
That refers to other people in
the scientific community that are being communicated
with.
So the answer directly is that no, there was no
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statement in there; but the people at that time and representing the public, like the Alabama AWIC, were informed as to what was going on.
Q. Sir, do the people who live downstream from
Monsanto's plant, are they considered to be just as important as your customers?
A. Sure. Q. All right. Do you believe that the people who
lived downstream from your plant in Anniston had the
same rights to know about environment contamination
problems as your customers did? A. I don't even know in 1970 or 1969 if there
were people downstream. Q. Sir, I'm asking you a simple question.
Sitting here today, do you believe that people who live downstream from your manufacturing facilities have the same right to know about environmental contamination problems that your facilities may cause as your
customers do?
MR. PECK:
19 -
THE WITNESS:
And that's exactly what we do
today and have been and I've already commented about the difference between the time frame that you're talking about and what were generally accepted practices for communicating this information.
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BY MR. GRAMMAS: Q. All right. And if there were people who lived
downstream from your plant in 1970 -- 1969, excuse me, when this memo was written, did they have every right to know about the environmental contamination problems that your plant was causing, at least as much as your customers had a right to know?
A. And I think at that point in time those communications were basically with the regulatory authorities who represent the public, and that was in essence a discharge of that communication obligation.
Q. And you knew on August 7, 1970, that the Alabama department charged with regulating it was going to keep this quiet from the public, didn't you? Monsanto knew that, didn't it?
A. Listen, we've been through these documents, it seems to me, before; and the answer to that is I don't know that that's what he says.
Q. The document says that's what he says. A. Well, but you read one line and I read the whole document, and if you read the whole document, I think you'd probably come to a different conclusion, too. Q. Mr. Pierle, you're trying to explain to me that you, Monsanto, discharged its obligations to
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________ __________.__________________________________________________________ 177
notify the public by telling state agencies about the
problem; am I hearing you correctly in saying that?
A. I think what I said very specifically was that
the normal practice at that time, if people even
communicated; and in many cases the question is:
Would
you even tell them? We did openly discuss this with
the regulatory agencies.
The regulatory agencies were
the governmental unit responsible for public
information.
Only in the late -- mid-'80s and late
'80s did the public get -- express their demand for
involvement directly in such information, and the
standard of practice has changed substantially.
Q. I didn't ask you anything about what you told
me, Mr. Pierle.
A. I answered your question.
Q. No, you didn't.
MR. PECK:
Yes, he did.
Don't argue with him,
Pete, just ask him questions.
MR. GRAMMAS:
Adam, stop telling me how to
take a deposition.
MR. PECK:
I'm not going to let you argue with
my witness.
MR. GRAMMAS:
I'm not arguing with him.
I'm
trying to move this thing forward.
MR. PECK:
Well, then stop asking questions
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and we'll move forward.
BY MR. GRAMMAS: Q. Mr. Pierle, we'll be here -- I don't care how
long it takes to finish your deposition.
We're going
to finish it.
It doesn't matter if it takes tonight,
tomorrow, we come back, we're going to finish this
deposition.
A. You're not -- you know, you're asking me to answer the questions you want me to answer in your way. I'm answering them truthfully from my knowledge.
Q.
I asked you:
Did Monsanto believe that by
disclosing things to the public -- to the state
agencies -- that it discharged its responsibilities to
disclosing it to the public?
A. I answered that question.
Q. And that's all I asked you, and you went into
a filibuster on what was standard practice in the '70s
and the '80s.
I didn't care about all that.
All I
want to know is:
At that time did y'all take the
position that if you told the Alabama agency charged with certain responsibilities about the environment
what you were dumping into the river, that you didn't
have to tell anybody else? A. I answered your question as truthfully and
honestly as I can.
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Q. Okay. There's a whole section in here on this confidential memo dated October 2nd, 1969, about PCB contamination, dedicated to notifying customers of
Monsanto; is that correct?
A. Yes.
Q. It goes on for pages; is that correct? A. I believe so.
Q. And there ain't nothing in here about notifying people who live downstream, is there, other
than notifying the government or whatever you said?
A. I think I've answered that question.
Q. Is that a yes? A. My answer is what I said it was. Q. All right. On Bates number 014621, in a
section, I guess, continued for the "Basis for Recommendations" title, there's a No. 4 section, titled
"Losses from Monsanto Plants." Did I read that correctly?
A. Yes.
Q. Mr. Pierle, did not Monsanto state in 1969
that, quote:
"It is impossible to establish a limit as
to what can be discharged 'safely,'" unquote, with
respect to PCBs? A. That's the statement that's contained here. Q. And again, that was 1969, right?
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A. Yes. Q. That was the same period of time that we know, based on prior exhibits, you-all were dumping about 250
pounds of PCBs into the river system in Anniston,
correct ?
A. Yes.
MR. PECK:
Object to the form of the question.
BY MR. GRAMMAS: Q. This memo that we're talking about goes on to
say -- let's follow up something for a second. Monsanto knew in 1955 that Aroclors were toxic,
correct, at some level? That's what Dr. Kelly said, do you remember that memo?
A. Yes. Q. All right. Monsanto knew in 1969 it was dumping about 250 pounds of this toxic chemical into
Snow Creek and into Choccolocco Creek, right?
A. We've been through that discussion of toxics,
yes . Q. And the dumping of the 250 pounds and all
that, do you remember the memo dated 1970 that we
talked about?
A. Yes. Q. Okay. And in 1969, that same period of time that you-all were dumping these toxic chemicals out,
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you-all had no idea what levels could be safelydischarged, did you?
MR. PECK:
Object to the form of the question.
No foundation.
BY MR. GRAMMAS: Q. According to that memo that I'm reading from. A. I think what that basically says is what it
says.
It doesn't know if there's a safe level of
discharge.
It goes back to the earlier memos around
toxicity, what do we know and what are we trying to
find out.
It doesn't say it's unsafe, it doesn't say
we don't know what is safe.
Q. And despite the absence of knowledge regarding what levels are safe, despite the risk that it very well could be that no levels are safe, because if you knew it was toxic in 1955, despite those things,
you-all continued to dump 250 pounds of PCBs out of your plant in Anniston into Snow Creek every single day
in 1969, not knowing what effect that would have on the environment, on the fish, or on the people that live
there, correct?
MR. PECK:
Object to the form of the question.
No foundation.
THE WITNESS:
I don't think that's what that
says .
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is;
BY MR. GRAMMAS:
Q. No, that's what I'm asking you. Knowing
everything now that we've read, isn't it true that
knowing all this knowledge, knowing the fact that you
didn't have any idea, Monsanto didn't have any idea
what levels were safe or not, it still dumped 250
pounds of this stuff into the creek every day.
A. I think what that document says is -- in its
entirety and why I read it is it lays out a very
aggressive program for saying we don't know if it's
safe.
We are now about significantly reducing the
discharges, the exposure, the use of the materials, and
basically we -- "safe" has to have an exposure
component to it.
There's nothing in here that says we
know about the exposure or the consequences of that
document -- of what was going on.
Q. That's right.
A. So I think that's a very aggressive plan at
that time to find out and reduce losses, to basically
be cautious about that -- about the knowledge that they
had, or the lack of knowledge, to secure more
knowledge, and too at the same time significantly
reduce the releases and, as it says in there, I think
someplace else, to minimal levels.
Q. I didn't ask you all that Mr. Pierle.
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MR. PECK:
Yes, you did.
MR. GRAMMAS: Adam, would you please stop interrupting?
MR. PECK:
Stop telling him what you didn't
ask him.
He's answering your questions.
He's going to
keep answering your questions.
You might as well stop
that preface because it's argumentative and it's improper.
MR. GRAMMAS:
Then just object to the form.
MR. PECK:
I'm getting tired of it.
I wish
you'd stop.
MR. GRAMMAS:
You just object to the form.
That's your role here.
MR. PECK: No, that's not my role.
MR. GRAMMAS:
Yeah, it is your role.
MR. PECK:
That's not my role.
You don't have
a right to argue with my witness.
MR. GRAMMAS:
I thought we said usual
stipulations?
MR. PECK:
You don't have a right to argue
with my witness.
MR. GRAMMAS:
Did we not say usual
stipulations?
MR. PECK:
Yes, and you do not have the right
to argue with my witness under whatever stipulations it
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is, wherever we are.
MR. GRAMMAS:
When we say "usual
stipulations," doesn't that mean, Adam, that you object
to the form and all other objections are reserved for
trial.
MR. PECK:
Yeah, but I can't just object to
the form and point out to you why I think it's improper
for you to argue with my witness, because we're not
going to do that, Pete, and if you keep it up, we will
just go.
BY MR. GRAMMAS: Q. Mr. Pierle -
MR. PECK:
I don't have to sit here and let
you treat my witness disrespectfully.
BY MR. GRAMMAS: Q. Mr. Pierle, I'm trying to get answers to
questions.
I'm not trying to be disrespectful to you,
but when I sit here and I ask you a fairly simple question and I get a filibuster, it aggravates me.
A. You're not getting a filibuster, you're
getting an answer that integrates the information that
you're putting in front of me.
Q. Well - A. And that's entirely appropriate to understand
the types of questions that you're asking.
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Q. Okay. We'll just do this little line in very
simple sentences.
In 1969, it was impossible for
Monsanto to establish a limit as to what discharges of PCBs could be done so safely, correct?
A. Yes.
Q. In 1969, at that same time period, sir, Monsanto was dumping 250 pounds of PCBs a day into Snow
Creek, correct?
A. Correct.
Q. In 1969, Monsanto was dumping 250 pounds of PCBs into Snow Creek and did not know what levels if
any were safe for PCBs to be discharged into that
system, correct? A. Could have been more than that could have been
safe.
Could have been less.
Q. Correct? A. I answered your question. Q. Okay. Don't you think that that's a conscious
disregard for the rights of people who live downstream
from you? A. No. It's a very responsible document and plan
to understand exactly what is going on and to take
responsible action. Q. This memo dated 1969, which is Plaintiff's
Exhibit 12, says that an investigation by Monsanto "has
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miles downstream from the plant, came from the Monsanto
plant ?
A. Well, I don't know what they concluded in
their mind, because it doesn't say that it came from
the plant.
They were certainly concerned about the
presence of that material and they were certainly doing
something about it.
Q. They never cleaned it up, did they?
A. I don't know that there was ever a need to
clean it up.
Q. Do you believe there's a need to clean it up
today?
A. I believe we're going to find an answer to
that question when we complete the studies with respect
to presence and whether or not there's risk and impact,
then we will know.
Q. These studies, according to this memo, should
have started back in 1969, shouldn't they?
A. I don't know what else transpired or happened
after that time period, series of conversations with
state and regulatory agencies about what should be done
or shouldn't be done.
I don't know what the end of
those conversations were. Q. According to this document, Exhibit 12,
studies should have been done back in 1969 to address
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186
shown that the waters in receiving streams below the
Anniston plant contain significant...concentrations of
PCB . "
Did I read that correctly?
A. Yes.
Q. But the more ominous concern of Monsanto at that time was "the fact that sediment in the bottom of
these streams miles below the plant may contain up to 2
percent Aroclor."
Did I read that correctly?
A. You're characterizing that statement.
Q. Did I read it correctly? A. I will read it as it's written, and I can't,
you know, do any better than that:
"More ominous
perhaps is the fact that sediment in the bottom of
these streams miles below our plants may contain up to
2 percent Aroclor." Q. Okay. This is in a section entitled "Losses
from Monsanto Plants," right?
A. Yes. Q. Now, isn't it a fact, sir, that in 1969 these
gentlemen who authored this, Mr. Farrar, Mr. Hodges, Mr. E.V. John, Mr. Richard, and Mr. Wheeler took the position and belief that the PCBs immediately below
Monsanto's plant, in the receiving streams and up to
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___________--_________________________________________________________ 188
and rectify the problems that we still have in Snow
Creek, Choccolocco Creek, and Lake Logan Martin with
respect to the PCB contamination.
Is that a fair
statement? A. It sounds to me like studies were done.
Q. Is that a fair statement?
A. Were being done.
Q. What I said, is that correct?
A. I would like -- you know, you're asking me a
question.
I don't know what the conclusion of this
exercise was.
If they did the studies and the
conclusion was we understand what's there, it's not a
hazard, then the answer today would be that everything
that was done at that point in time that was
appropriate was done.
I don't know what the next set
of steps and information was as a result of these data,
studies, and findings.
Q. How much money has Monsanto put aside to conduct this process that you keep talking about to
determine whether or not some remediation needs to be
done to Snow, Choccolocco Creeks, and Lake Logan
Martin? A. Whatever we -- I don't know the exact number
whatever we estimate at this point in time the cost of
those studies to be.
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Q. You're responsible for establishing the reserves that this company's going to put aside to address these problems?
A. Yes. Q. What are the reserves currently?
A. I don't know. We have reserves for up to,
like, 200 projects.
I don't know in detail each
line-by-line item.
In the aggregate, it's something
like $200 million or something a little less than that.
Q. For the Anniston plant?
A. No. Q. That's what I'm asking you.
A. No, it wasn't. You asked me what were Monsanto/Solutia's environmental reserves for projects
like this.
I told you I don't know what the cost in
the reserve is for the Anniston plant.
Q. Do you have a guesstimate?
A. No. Q. Is it less than $100 million?
A. I already indicated to you that we have $200
million in aggregate.
We have no projects at that
level.
Q. Is it less than $20 million?
A. Listen, you're going to walk me down number by
number.
I told you I don't know what the number is.
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That's my answer.
Q. And you're the man responsible for setting it
up?
A. Yes.
Q. Now, the number -- I know you don't know, but
it's certainly in the millions of dollars; you'll agree
with me on that?
A. Listen, I told you I don't know.
Q. All right. Well, you're willing to embark
this company, Solutia, on a course of events to spend
whatever sum of money you've set aside, but can't
recall, to study this problem of PCB contamination in
this ecosystem, right?
A. Yes, we are. Q. And in doing that, you don't know whether
those studies have already been conducted back in the
late '60s and the '70s which have already determined
that there wasn't a problem at all?
A. What I know is we are about a set of studies
today.
That's what I know.
I don't know what went on
in the past in detail.
Q. I thought you testified moments ago, sir, that
in 1969/1970 when these memos say, Hey, we need to go
out and do some studies to figure out what's going on
out here, I thought I heard you say that you may have
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very well done that and concluded that there was no
problem.
Did you not say that?
A. I didn't say I knew that.
Q. Well, I know. You said that you may have done
that and you may have decided that there really wasn't
a problem out there with respect to PCBs, didn't you?
A. Yeah, "we" being the vernacular with the
government people and everybody that was involved.
Q. If that were the case, sir, don't you think
that would be something you'd want to know right now
before you embark on this course and spend all this
money unnecessarily to study a problem that you've
already determined doesn't exist?
A. My belief would be that the people that work
for me know that in detail, we know where we are in the
conversation.
Today is not the 1970s, today is the
1990s and we feel committed that it's appropriate to do
additional studies, and that's what we're about.
Q. We've identified some environmental
guidelines, I believe it's Plaintiff's Exhibits 6 and
7. It's the 1989 guidelines that dictated you-all's
course of conduct during that period of time up through
1992, and the 1992 Monsanto pledge guidelines under
your signature that dictated Monsanto's responsibilities from then up until 1997 and Solutia's
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responsibilities from September 1997 through today,
correct ?
A. Yes. Q. Now, this one. Exhibit 5 -
A. With the provision that this draft is --
Q. Right, may replace it. And that's where I was
going to.
This one may replace it, but it hasn't yet.
A. Some of the practices in here, we may have
already made judgments and decisions on what needs to
be changed.
So, again, this is a working draft to
adopt a set of decisions that we have made.
Many of
those are made - - as I indicated, are relatively
low-level decisions, so it's conceivable that this
document is reflecting changes that are already
acceptable practices in Solutia.
Q. Now, where in these two exhibits, sir,
Exhibits 6 and 7, that you were instrumental in
creating, does Monsanto, and now Solutia, address the
issue of PCB remediation?
Is it in this section
entitled "Corrective and Remedial Action"?
A. I'd have to go back and look at the documents
again.
I mean, that's not a document that I pull out
and read every day. Q. Now, let me ask you: You've read this part of
the document already. Corrective Remedial Action.
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We've been through that earlier, before lunch, do you
recall that testimony?
A. Yes.
Q. Doesn't that section deal with PCB-related issues ?
A. It would deal with it with respect to
remediation activities associated with it.
Q. Right. Is that the only thing that you're
aware of, sitting here today, that dictates how
Monsanto, and now Solutia, should deal with
PCB-remediation issues?
A. You know, there are other general rules around
PCB use and regulations and requirements and systems
and we basically say we'll comply with all rules and
regulations.
So whether specifically referenced, if
there's anything to deal with that on a regulatory
matter, they're probably addressed generically in other
sections.
Q. But as far as a cleanup activity is concerned,
and in particular here at Anniston where we know
thousands of pound of this stuff was discharged from
the plant, this Corrective Remedial Action section in
the 1989 environmental guidelines dealt with how
Monsanto would remediate issues up until 1992, correct?
A. It dealt with remediation matters in general.
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Q. Right, but it covered PCB-remediation issues,
that's what I'm getting at, right?
Well, let me ask you this:
If I go up to a
jury and I say, I spoke with Mr. Pierle directly, the
man who was intricately involved in creating this
document, would I be correct, Mr. Pierle, in saying that you believe that from 1989 until 1992, the section
entitled "Corrective and Remedial Action" dictated how
Monsanto should go about remediating PCB-related issues
in the river system in Anniston? Would I be correct in
saying that?
A. I think that's generally correct.
Q. Now, I assume you have similar language in the
Monsanto pledge guidelines, do you not?
A. I believe so.
Q. I'm trying to find them. I've read them.
Are the people who live downstream from your
plant -- strike that.
Are the people who lived and still live
downstream from the Monsanto plant, and now Solutia, in
Anniston considered stakeholders of the company?
A. I think, in the broad definition of the
"stakeholders," we include communities and, you know,
people in and around the plant site.
Q. Because when I read -- this is Exhibit 6,
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under Worldwide Guideline No. 6, "Product Stewardship,"
it says:
"Monsanto products and intermediates will not
present an unreasonable risk of harm to human life or
health or to the environment when they are properly
handled, transported, used, or disposed.
Stakeholders
will be provided information regarding" -- what I just
read.
And then it says:
"Employees, customers, and
the community are all stakeholders."
So that basically answers my question that I
just asked you, correct?
A. Yeah. I think in this case, because we deal
with it in different sections, that, you know, product
stewardship deals with the community of people who are,
you know, associated with customer use and that of
product.
I think we deal with communities in general
around plant sites and that is in additional sections.
Q. But here under, "Product Stewardship,"
stakeholders were defined as the community, right?
A. Yeah.
Q. And that would include -
A. I'm suggesting that that community may be a
different community around where we make the product.
Q. So that community does not mean the people who
live downstream from the plant?
A. I think what I said was they are covered in
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this document in additional sections.
They're very
important. Q. In determining what actions Monsanto will or
should take with regard to any PCB remediation in Snow
and Choccolocco Creeks and Lake Logan Martin, Mr.
Pierle, isn't it a fact that you or people under your
instruction will rely on the types of documents and on
these very documents that we have identified in your
deposition today as Exhibits 8, 9, 10, 11, and 12 -
MR. PECK:
Object to the form of the question.
BY MR. GRAMMAS: Q. --in determining what steps if any need to be
taken?
MR. PECK:
Object to the form of the question.
THE WITNESS:
I don't know to what extent
these documents exist, you know, outside of this
litigation process, you know, if they're generally
available.
We're going to rely on whatever
information, you know, we can gather to help us
understand the factual situation that I described
earlier.
BY MR. GRAMMAS: Q. And are you aware of any individuals that are
still alive today who worked at the Monsanto plant who
may be able to provide testimony or information to you
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in your fact-finding mission to determine what impacts you-all's plant had back during this period of time?
A. Well, I know that Mr. Papageorge is still alive and I believe Mr. Jessee is still alive, but the
balance I don't know.
Q. Do you know where Mr. Jessee is? A. No, I don't.
Q. What makes you think he's still alive?
A. Well, I mean, it's sort of by deduction.
Typically inside the company when people pass away,
there's some sort of notice.
I don't recall having
seen one, so I conclude from that that he is probably
still alive.
Q. Do you have any idea how old he would be, or
Mr. Papageorge, how old they are?
A. I think Mr. Papageorge would be in excess of
70.
Mr. Jessee, I'm not sure.
Q. If you-all needed to -- first of all, do you
believe you need to understand what conduct occurred in
the past at the plant in order to properly assess what
remediation, if any, needs to be done today?
A. I don't think we need to understand -- well, I
don't know what you mean by "conduct."
I think we need
to understand, as best we can, you know, facts. Q. Like how much PCBs were put into the river
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system and things like that?
A. It would be useful. I would say, you know, in any one piece of information, probably not critical.
As you go through these studies, it's more critical to understand how much is there, is it exposed to anyone,
is there a risk, is there remediation.
These kind of
documents would go more to allocation of
responsibilities.
Q. Yeah. That's really what I'm getting at. These documents will be viewed internally by Monsanto
as to what extent, if any, it was responsible for
putting PCBs into the river system that they're being
sued over today?
A. As I said, my sense would be that -- to the
extent that they're generally available.
I don't know
that they are.
They're probably relevant, but I don't
know the importance of the documents in the work that
we have underway.
Q. Who's Mr. Hanley, Mr. John W. Hanley, do you
know who he is?
A. Could I see the note? Q. Yeah, I'm going to show it to you in a minute, but do you know who he is just off the top of your
head? A. There were several John Hanleys in Monsanto,
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so I don't know -- there was a guy that was a CEO.
There's guys at different levels.
There's more than
one John or Jack Hanley that has existed in Monsanto.
Q. What involvement, if any, did you have with
PCB-remediation issues in 1975?
A. I don't believe any.
(PIERLE EXHIBIT NO. 14 WAS FIRST DULY
MARKED, RECEIVED AND MADE A PART OF THE RECORD.)
BY MR . GRAMMAS : Q. I'm going to show you what's been marked as
Plaintiff's Exhibit 14 and ask you if you can tell me who Mr. Hanley is? His name and title appear at the
end of the document as having received a copy of it.
A. Well, the back page says he was president of
Monsanto Chemical Company, so I think that describes
who he is.
Q. Did you ever have any conversations with Mr.
Russell Train, the administrator of the United States
Environmental Protection Agency, in 1975?
A. No. Q. Have you ever had any conversations with him
at any time? A. I think I met Mr. Train several years
subsequent to that at an environmental law institute
dinner and said hello.
That's about it.
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Q. Do you agree with Mr. Train's assessment of the PCB issues that are contained in highlighted portions of this letter? And I'll read them for the
court reporter:
"For at least five years, the Federal
Government and the manufacturing industry have been
aware that polychlorinated biphenyls (PCBs) pose a
threat to human health and the environment.
Last
month, at EPA's national conference on polychlorinated
biphenyls in Chicago, leading experts clearly
documented the fact that PCBs are pervasive in the
environment, are causing disruptive and economic harm
to commercial fishing in many areas, and are creating a
serious potential health hazard to the public."
Do you agree with those statements, sir,
sitting here today?
A. I think what we've said before, that with
respect to the human health impacts of that, we have a
different viewpoint.
Q. But everything else you agree with?
A. The "everything else" being basically that
there are impacts on wildlife and fishing, and that was
again what we felt was the principal concern.
Q. I'm being more specific. Everything else that
I read out of this letter you agree with other than, in
your opinion, PCBs' effects on humans? And I'm talking
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about just the highlighted sections that I read.
A. I think with the exception of the words "human health," we don't agree with that, and again, my
comment on environment, yes, we agree that there were
areas of concern with that.
That's what was driving,
you know, our thinking and our work.
Q. And there still are areas of concern as of
today?
A. Well, I think that's what we're -- in part
what we're looking at.
Q. And it's also what this lawsuit's about, isn't
it, according to your understanding?
A. I believe those are the allegations. Q. Tell me, sir, all the ways you're aware of, as
the environment manager, the head environmental manager
at Solutia, to properly dispose of PCBs.
And I don't
mean PCB-contaminated material, I mean during the
manufacturing process, if you had some waste that was
being generated, what are the proper ways that you're
aware of to dispose of them?
MR. PECK:
Object to the form of the question.
Foundation.
THE WITNESS:
Today?
BY MR. GRAMMAS: Q. Yeah, today.
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A. I think the requirements are -- well, nobody
makes PCBs.
There are PCBs in the systems.
I think
you can incinerate them, although there's some pressure
against incineration in general.
I know there are
other technologies working at decoupling carbon atoms and then trying to work with the residual materials,
but I think if you were generating a liquid waste
today, emptying a transformer or something, I think
that you'd pretty much have to burn the material. Q. Could you throw it into a river system?
A. I don't believe so.
Q. At any level?
A. I don't think so. I think there are
regulations against spilling and dumping of this at
pretty low levels. Q. We're going to jump out of sequence here.
Earlier I was asking you -- with respect to PCB-related
remediation issues, I directed you to Exhibit 6 to your
deposition, which is the '89 guidelines in effect
through '92, and particularly the corrective and remedial action section, and asked if that was the
policies, procedures, and ways that Monsanto during
that period of time would have or should have gone
about remediating PCBs, do you recall those questions?
A. Yes.
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Q. And I believe you said that it was in fact the guidelines that they should and would follow, correct?
A. Yes. Q. All right. Now I'm going to show you the
Monsanto pledge guidelines, what Mr. Lowe just found
for me, and ask you if you would read the title
"Superfund."
It's not entitled "Corrective and
Remedial Action," which is probably why I couldn't find
it.
Are those the same guidelines in general that you
would apply in cleaning up or remediating PCB-related
issues today?
MR. PECK:
Just for the record, you're looking
at Plaintiff's Exhibit 7.
MR. GRAMMAS:
It's the Monsanto pledge
guidelines.
THE WITNESS:
I think that's generally the
practices that we're using today.
BY MR. GRAMMAS: Q. That would apply even if the PCB-related -- or
the PCB contaminants you were going to remediate were
not related to a Superfund site, correct?
A. In general I think that's correct, yes.
Q. Like for example, this is the exact guideline
you expect to follow in deciding whether or not to
remediate the PCBs in Snow Creek, Choccolocco Creek,
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and Lake Logan Martin, right? A. I think this describes the behavior that's
expected and that's what we would follow.
Q. And that's what you should follow?
A. Sure.
Q. And again, that's -- for the record, it's the
Monsanto pledge guidelines dated under your cover
November 11, 1992, Section 6.4, entitled "Superfund,"
correct ?
A. Yes .
MR. PECK:
Let's take a break.
(A SHORT BREAK WAS HELD.)
BY MR. GRAMMAS:
Q. Mr. Pierle, do you think it's responsible for
a company to discharge hundreds of pounds of chemicals
into a system, knowing that the chemical is toxic,
while at the same time not knowing what safe limits
there are?
A. Back in 1968, '69, '70, I think that was
acceptable practice.
Q. Could you define for me, sir, all of your
current job responsibilities.
A. I an responsible for remediation matters, as
we have discussed here today.
I'm responsible for
providing to Solutia, the entire enterprise, services
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as are needed with respect to product stewardship support and sort of following governmental regulations and the development of company policy where appropriate.
Q. Regarding environmental issues? A. Environmental health and safety matters, and we also provide services, again to the entire organization, technical services and scientific services, engineering services and regulatory services needed to comply with laws and regulations. Q. And with respect to environmental issues, health and safety issues, and remediation, is there anyone within Solutia more senior to you, sir? A. No. Q. In 1983 when you were charged with the responsibility of - A. I'm sorry, what year? Q. In 1983. A. '83 . Q. I know we're jumping out of context.
In 1983 when you were charged with the responsibility of being the regulatory manager and director of hazardous waste -- do you recall those responsibilities?
A. Yes.
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Q. -- did that include PCB-related issues for
Monsanto?
A. Not specifically.
Q. You currently sit on the board of directors at
the Chemical Institute of Toxicology?
A. That's correct.
Q. Does that institute involve anything -
involve itself with any PCB-related issues?
A. No. Q. Has it ever?
A. I don't believe so.
Q. What does it take for a company to get the
president -- for Solutia, I guess, to get -- actually,
it wouldn't be.
What would it take for Monsanto and/or
Solutia, a plant within the company, to get the
president's safety award?
A. We annually look at safety-related
performance.
This is basically personal safety in the
workplace, and we look at the best performers.
Q. Receiving that award doesn't have anything to
do with, like, PCB discharges, exposure,
responsibilities for cleanup, that type of stuff?
A. No. Q. Is the Monsanto site a PCB-free site, sir --
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excuse me, Anniston.
MR. PECK: Anniston.
free?
THE WITNESS:
The Anniston site, is it PCB
BY MR. GRAMMAS:
Q. Uh-huh.
A. I believe it is by our terminology on "PCB
free. "
Q. Could you tell the world that, We're PCB free,
without explaining what that meant? Could you fairly say that you're PCB free without explaining what that
means in your terminology?
A. I don't know how to answer that. Are you asking me to answer it?
Q. Well, you just said if someone held themselves
out, someone within Solutia held the Anniston plant out
as being PCB free, don't you think that would be a bit
misleading to the public if they didn't also give them
Monsanto, and now Solutia's, unique definition of what
it means to be PCB free?
MR. PECK:
Object to the form of the question.
THE WITNESS:
I don't know that that would -
what was your term, "irresponsible"? What term did you
use .
MR. PECK: Misleading.
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THE WITNESS:
I don't believe so.
BY MR. GRAMMAS:
Q. So you think someone could fairly tell a group of people, We're PCB free, and not feel like that's
misleading to them without explaining what that means?
A. I mean, I think that they would or that
someone would probably ask, What do you mean by that?
Q. And what do you mean by that?
A. We established a program some years ago, with
respect to use of PCBs in the systems, that we would
remove PCBs from active use within our facilities.
That means if we were using some sort of an electrical
system, that we would be PCB -- in other words, we
would get the PCBs out of those electrical systems.
Q. But that's not to say or suggest to anyone
that there aren't any PCBs on your property down there in Anniston, is it?
A. No, that was not, you know, the definition in
which that was intended.
Q. Now, how many pounds of PCBs are currently
stored on the Monsanto property?
A. I have no idea whether any are.
Q. You don't know that out at the West End
Landfill there are thousands of pounds of that stuff
being stored out there?
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A.
Yeah.
Again, we were talking about active,
utilizable PCBs, and when you asked me that, I was in
that follow-up question.
Q. No, I'm just talking about PCBs in general.
That's the confusion of saying, We're PCB free.
Nobody
really knows what that means.
But when I say, How many
pounds of PCBs are out there right now? I mean in any
shape, form, or fashion, stored in landfills, barrels,
whatever.
A.
I don't use the word "stored."
They're
disposed, properly disposed.
That would be my
terminology.
When you deal with respect to the
"landfill," if you use the word "stored," my definition
would be different.
So, as you say, it's important to
understand the definition of terms.
Q. How many pounds of PCBs are out there?
A. I don't know.
Q. How many landfills are on the Monsanto
property? A. I think we've dealt with two. I think --
Q. And both landfills have PCBs in them, right?
A. I think that they have PCBs or
PCB-contaminated materials.
Again, I'm uncertain, but
they do have PCB in them. Q. There are regulations that are in existence
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today that discuss the methods by which a company must
dispose properly of PCBs found, like, in soil, which
are 50 parts per million or greater, aren't there?
A. Yes. Q. And what do these regulations require?
A. They're kind of complicated. I know they
exist to deal with, you know, current waste and
produced waste of materials.
Q. And you're --
A. I don't know exactly what they are. People in
my organization know the answer to that question and I
expect them to know it and they do.
Q. And you expect them to follow -
A. Yes. Q. -- the regulations?
A. Yes. Q. That would mean that if something was greater than 50 parts per million in sediment, let's say,
that's supposed to be stored in a hazardous landfill,
isn't it?
A. No.
MR. PECK:
Object to the form of the question.
BY MR. GRAMMAS:
Q . It's not ?
A. No.
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Q. There are no documents that I can read in
Monsanto's possession that say. When we collect these samples of dirt out at Snow Creek, if it's greater than
50 parts per million, we should take it to a -
A. I don't know what the requirements are with
respect to sampling or -- I mean, we would -- the
documents would say that we should comply with the
regulations.
Q. Well, what I'm asking you is: Back in the '89 time frame when you-all were remediating the Snow Creek
issues and getting PCBs out of the Snow Creek portion
that the attorney general is dealing with, are you
aware of any requirements that that sediment, that
soil, once it dried and was measured to be greater than
50 parts per million PCBs, should have been taken to a
landfill in Alabama that was designated as a hazardous
waste landfill?
A. I don't know what the regulations were at that
time . Q. Do you know where that dirt went, that soil?
A. No, I don't.
Q. Do you know that it went out to your landfills
right there on site?
MR. PECK:
Object to the form of the question.
THE WITNESS:
I don't know that.
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BY MR. GRAMMAS: Q. Do you know whether the landfills on site are
hazardous waste landfills?
MR. PECK:
Object to the form of the question.
No foundation.
MR. GRAMMAS:
I'm asking him if he knows.
That is the foundation.
MR. PECK:
Well, your question assumes facts
that are not in evidence.
That's why I'm objecting, if
you want to know why I'm objecting.
They
mischaracterize his testimony in the case.
BY MR. GRAMMAS: Q. Do you know whether or not, Mr. Pierle, the
landfills out there on the Anniston plant are
hazardous -- or, qualified to be hazardous waste
landfills?
MR. PECK:
Object to the form of the question.
No foundation.
THE WITNESS:
I'm not specifically aware of
what their regulatory designation is today.
BY MR. GRAMMAS: Q. Do you know if they're Subtitle D landfills?
A. I don't know. Q. Have you outlined in your mind or have any of
your managers under you outlined a flow chart of
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possible scenarios that may occur with regard to the PCB-remediation issues in Snow Creek, Choccolocco Creek, and Lake Logan Martin?
A. I have not seen anything. Q. Okay. What is the best possible scenario, in your mind, that could result out of this process that Monsanto is now undertaking as it relates to whether it's going to clean up the PCBs in this area? A. That a remediation properly determined by the process of the health and the environment is implemented. Q. Is the best scenario, in your mind, a determination by the people you hire that no remediation is necessary at all? A. I think we're in the process of trying to develop the answer to the question that you're asking, so I don't have a prejudgment about that. Q. Well, I know I don't have a prejudgment, but sitting here today, can you not tell the members of this jury that the best possible scenario for Monsanto would be that there doesn't need to be any remediation at all? A. No, I can't say that.
Q. The worst possible scenario for Monsanto, sir, would be what?
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A. I don't know. Again, there is only one scenario, I think at the end of today, with respect to remediation, and that is we come to a determination as
to what the process yields as a conclusion and that's
the remedy that's implemented.
Q. So as the highest executive officer in health,
environment, and safety Mr. Pierle, is it your
testimony, then, that if this process that you-all are
undergoing reveals that Monsanto should remediate all
of the PCBs in Snow Creek, Choccolocco Creek, and Lake Logan Martin by some form of dredging operation and
remove them entirely from the system, that Monsanto would be willing to do that?
A. I'm not going to speculate to that
hypothetical because I think we're going to have to ask
whether or not that's the outcome of the process.
Q. Well, I'm asking you -
A. Dredging is not a typical answer to these
sorts of issues.
So my general inclination is that's
probably not probable, but I'm sure it will be looked
at . Q. Let's talk about the different possible
outcomes with respect to this remediation issue.
At
one extreme, an outcome is that Solutia/Monsanto does
nothing, right?
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A. I guess that's always an option.
Q. Do you think that's a very likely option, sir, given all the information you know as the environmental
manager over this problem?
A. I've learned long ago not to speculate or try
to guess what a probable or possible outcome is.
It's
fact-specific and you can't make a judgment from one
site to another as to what's probable, and we'll find
out what the answer to that question is.
Q. And Monsanto has known about this problem,
according to the documents we've produced today at least, since 1969, right?
A. What problem? Q. The PCB problem at Snow Creek, Choccolocco Creek, Lake Logan Martin.
A. I think the documents speak for themselves,
without going back through them.
I didn't see anything
in this relative to Lake Logan Martin.
Maybe I missed
it, but -Q. It was dealing with Snow Creek and Choccolocco
Creek, but now we know that it's in Lake Logan Martin,
right, PCBs? A. I think there's a fish advisory, so there's
knowledge, and I think that lake and the area is being
studied.
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Q. Now, 30 years of knowledge hasn't been enough time for Monsanto to figure out this problem, and now Solutia has it.
A. I think I have responded that we have been
very aggressively working on the issue since it came
about in '93 or thereabouts and we're moving as fast as
we can towards understanding and resolution. Q. Well, the issue came about in 1969, didn't it,
sir, according to you-all's documents?
A.
I don't know what the issue is.
You're
describing --
Q. PCB-related problems. PCB discharges into
Snow Creek, Choccolocco Creek?
A. You're talking about the presence of PCB.
That is different than a problem.
So you're talking in
these documents about the presence of PCBs. Q. Like you said, the documents will speak for
themselves and they call the PCBs "problems" on
numerous occasions and we don't need to go back through
that.
What I'm saying is:
Monsanto's been aware of
the presence of PCBs in this river system for over a
30-year period -
MR. PECK:
Object to the form of the question.
BY MR. GRAMMAS: Q. -- and that amount of time has not been long
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enough for you-all to figure out whether doing nothing is a possible scenario to this problem, correct?
MR. PECK:
Object to the form of the question.
THE WITNESS: Again, looking at the
involvement of the agencies over time, the fact that
what needed to be done got done, as we've discussed
with respect to Snow Creek, the information in the
'70s.
So I have to conclude from that that the actions
that were appropriate relative to the knowledge that
was in hand, those actions were taken.
BY MR. GRAMMAS: Q. I understand you're going to conclude that
you-all didn't do anything wrong.
My question, though,
is:
Based on this almost 30-year period, from 1969
to -- it's almost now 1999, and knowledge that PCBs are
getting into this system, this river system, that
period of time has not been long enough for Monsanto,
and now Solutia, to at least determine that they're not
going to do anything about the presence of the PCBs in
the river system, right?
MR. PECK:
Object to the form of the question.
THE WITNESS:
You keep mixing "over 30 years,"
"is"getting
into the system.
I think the information
we've talked about is -- you know, the information
about what was getting into the system was the subject
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of the '70s reduction program.
There's nothing I see
where it's getting into the system.
The '80s system
around Snow Creek, whatever Snow Creek is in that
determination, was what was there was removed.
The
discussion about '90s, about what could be getting into
the system around the storm water runoff is what -
again, when we said there's evidence here that
something may be getting into the system and we need to
go act and do something about it.
Q. Another possible scenario, rather than doing
nothing, is to do some type of cleanup, is it not?
A. Well, when you look at remediation options,
they range from do something to what looks like is technically/economically/environmentally feasible, and
that's what we expect this study to help define for us. Q. One thing is to do nothing, right?
A. Yes. Q. That's one scenario -
A. Right.
Q. -- where you just leave it there and just let
it be .
A. Right.
Q. The next scenario is some form of cleanup,
correct? A. I don't want to mince words with you. We're
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talking about remediation, you're using "cleanup."
Another option is to do something.
If one's to do
nothing, then there's an option to do something.
Q. Right. Let's talk about some of those
options.
One extreme is to do nothing, the other
extreme is to dredge the entire river system and take
out every PCB that's found in there that's humanly
possible to do; isn't that another situation?
A. I think I've answered that question. I see no
value in speculating as to what possibilities are.
I
think we need to stay in the process we're in to
identify what those possibilities are within, again,
the process that we're in, and that will tell us what
the range of possibilities are.
Q. Have you read any of the expert reports that
the plaintiffs have submitted to this Court, sir?
A. No. Q. So you're not in a position to disagree with
any of the opinions that those experts have provided
today, are you?
A. Listen, I'm dealing with the remediation
question associated with this as best we can.
The
lawyers are dealing with the third-party litigation and
the property damage claims and I'm focusing on the
remediation process.
That's what I'm focused on.
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Q. And in your mind, the two don't overlap in the least bit, do they?
A. I don't know whether they do or not.
Q. So you're not going to tell me today, as the head environmental manager, what the possible scenarios
of remediation could be.
A. No, I'm not. I mean, I rely on a lot of
people and we have consultants and the whole process
around the United States yields answers to that
question.
People don't sit in chairs and pontificate
over it.
I'm not going to do that.
Q. And you don't want the jury who's going to
read this testimony to know of the possible scenarios
that the head manager over environmental affairs and
remediation thinks may exist with respect to any
cleanup, if there is one?
A. I would hope that the jury would ask what's
the process by which those are determined and whether
or not those remedies were being appropriately looked
at. Q. Have you been informed by any of your managers
or are you aware that the lawsuit that you're here today to testify about also involves remediation as a
claim? A. I've heard that there are attempts to get at
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the question of remediation in the lawsuit, but again,
as I said, I'm dealing with the Alabama authorities and
the question of remediation.
That's the issue that's
in my domain and that's what I'm dealing with.
Q. Do part of those Alabama authorities that you're dealing with, does that include the judge who's hearing this case and who will be hearing the plaintiff's claims for remediation cleanup?
A. I don't know what the judge is going -- we're
dealing with the regulatory authorities.
Q. I understand that. A. The lawyers are dealing with the judges.
Q. Are you aware, as a manager, as the manager of environmental affairs and safety-related issues for
Solutia, that this judge may very well order this
company that you work for to do some type of cleanup of the PCB problem we're alleging exists out there in the
river system?
MR. PECK:
Object to the form of the question.
BY MR. GRAMMAS: Q. Are you aware of that fact? A. I think I answered that. I think that I said
I understand that may be part of that case and that discussion, but the focus and the process that we're in that's leading to that answer, that I'm involved with,
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is the remediation discussion with the agencies.
Q. And this process that Solutia is engaged in and has embarked upon to determine what remediation if
any should be done, are they hiring contractors to do
work to study these issues?
A. I believe so.
Q. Do you know the names of these contractors?
A. No, I really don't, not all of them.
I mean,
we've had a variety of different contractors doing work
down there.
Q. Do you know if any of the contractors that
you're hiring to, I guess, make these findings are
being retained by your company to provide expert
testimony in this lawsuit?
A. Again, that process is managed by the law
department.
I don't manage that process.
Q. Have you paid any contractors to determine
what sources other than Monsanto may have been
responsible for putting the PCBs in Snow Creek,
Choccolocco Creek, and Lake Logan Martin that are being
detected as we sit here today?
A. I think that work -- there is work ongoing on
that as part of the whole study.
I don't know who's
directing that work. Q. You don't know which contractor is responsible
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for doing that?
A. No. Q. Which one of your managers is responsible for
making sure that gets done?
A. Well, again, I don't know whether it's one of
my managers or whether that is coming from the law
department.
Q. Okay. Sitting here today, sir, as the head
environmental manager of safety and health and
remediation for Solutia, can you identify a single
source other than Monsanto that may have been
responsible for putting the PCBs into Choccolocco
Creek, Snow Creek, and Lake Logan Martin?
A. Well, as I said earlier with respect to the
close end, the person that used PCB materials out of a
metal mill, and I don't know what kind of metal.
There
was some question as to whether or not there was
someone further down Snow Creek.
There are other
entries, as I understand it, into Choccolocco Creek and
into the lake that need to be looked at, and one of the
hardest things to find in some of these cases is
whether or not, you know, folks have done any kind of
dumping over time, and we've found at times you have to
ask that question, as well.
So I would assume that all
of that is being looked at.
That would be typical to
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what we would look at ourselves or with other PRPs in an examination of a site.
Q. Tell me the names, Mr. Pierle, of sources other than Monsanto that contributed to the PCB problem that we have been talking about all day today?
A. I've categorized them the best I can. Q. Do you know the names?
A. I do not know the names.
MR. PECK:
You just don't like the answer,
MR. GRAMMAS:
"I don't know of any," is the
answer.
MR. PECK:
That's not the answer.
The answer
is he doesn't know the names.
He categorized
possibilities for you, Pete.
BY MR. GRAMMAS: Q. But you can't identify a single name of a
single person or company that's done -
A. I do not know the names.
Q. Okay. And by your own testimony, Monsanto's
been looking at this problem since the early '90s,
right?
A. Yes. Q. It's over eight years, by your testimony.
A. I think that we said 1993 . Q. All right, five years. Five years, right?
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A. Yes. Q. And sitting here today, on this five-year
study that you-all have been doing, nobody's come up to
you and said, Mr. Pierle, guess what, we've learned
that A, B, C, D, and E are pumping -- discharging PCBs
into this river system, it's not us, it's them.
Nobody
has told you that, have they?
A. That hasn't been the primary focus of what
we're doing today.
Q. I didn't ask you if it was the primary focus,
Mr. Pierle, I asked you if anybody's ever told you
something like that?
A. They have said that we have information or
indications that these couple of people that I've
described are potential contributors, yes.
Q. Have they ever come up to you and said, You
can remove the word "potential," A, B, C, D, and E are
contributing to this problem?
A. We never -- I mean, PRPs, part of -- you never
remove the word "potential."
I mean, it's part of the
vernacular.
Q. So when you say Monsanto is a -- do you
believe that Monsanto is a potential responsible party
for the PCBs in this system?
A. I think I've answered that before.
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Q. I didn't hear the answer, if you did. Do you believe that Monsanto is a potential responsible party for the PCBs in the river system at -
A. And my answer was that on the information we have, we're acting according to our policy that we
certainly could have potential responsibilities here.
Q. And when you say "potential" here, you just
mean that in the vernacular, and really you can take
that word out of the sentence and say, yeah, we have
responsibilities?
A. That's not what I said.
Q. Okay. Let me ask you this: Do you believe
this is a frivolous lawsuit, sir?
A. Others are going to answer that question.
Q. What is your personal opinion as an
environmental manager?
A. As soon as I know more facts about the
situation, I'll be better able to understand that.
My
understanding to date, there are fish restrictions on
the lake.
I don't know the extent of concern that
causes or how that supports a base for lawsuit.
I
really don't know. Q. Do you own any lakefront property, sir?
A. No. Q. Have you ever owned any lakefront property?
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A. No. Q. Are you a fisherman? A. Very, very seldom.
Q. Do you like to eat fish?
A. Sure.
Q. Would you eat fish out of a river where a
state agency has posted signs all up and down that river saying: Warning -- I think it says -- Public
Health Advisory:
Do not eat the fish out of this river
system? A. I think based on what I know, I probably -- it
wouldn't bother me to do that infrequently.
Q. Would it bother you to do that frequently?
A. I probably wouldn't. I'd say, What are my
other options and what else can I do?
Q. And that's because you don't want to expose yourself to any undue risk of having adverse health
effects, right?
A. I don't know whether it's that. It's just,
you know, do I need to do that or don't I? Do I need
to eat those fish?
I don't know that it's that clear
in my mind. Q. If Monsanto is found to be substantially -- is
found to be a substantial or part contributor to the
PCB problem in this ecosystem that we've been talking
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_____________________________________ _____________________ _
about today, sir, and is responsible for the fish advisories posted out there, do you believe that Monsanto should take action at a minimum that would allow the state of Alabama to remove the fish advisories?
MR. PECK:
Object to the form of the question.
THE WITNESS:
I think that's a pretty complex
question.
At that point we'd be taking some actions in
conjunction with the State and others that I would
assume all would agree is appropriate.
Whether that
would result in the elimination of those advisories, I
don't know.
Q. What I'm saying is: If Monsanto's conduct
caused the fish advisories to be put up there, don't
you think Monsanto should do whatever -- and now
Solutia, should do whatever it takes to remove the
problems that are causing the fish advisories to be
there?
MR. PECK:
Object to the form of the question.
THE WITNESS:
I think if the people that are
involved in this process determine that that is not an
undue problem versus other potential remedies and
that's the collective judgment and decision that's
made, I don't know that we'd do more than that.
BY MR. GRAMMAS:
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Q. Okay. Who's making these collective decisions
that you keep talking about? Monsanto certainly's
going to be part of it.
Who else is going to be a part
of it?
A. Well, the State and the regulatory people and
the public's involved in this process, and that's going
to generally -- you know, that's the process for making
decisions about remediation.
Q. And I know you don't want to guess or
speculate about what may come out of this study, Mr.
Pierle, but what I'm hearing you say is that after
Monsanto spends all this money to conduct the studies
to see what if anything needs to be done, it may very
well be that the fish advisories that are posted all
along that creek won't come down as a result of any of
your conduct, true?
MR. PECK:
Object to the form of the question.
THE WITNESS:
I mean, it seems to me that's a
possibility.
BY MR. GRAMMAS: Q. And you can't tell me -- you're a man, as you
testified earlier, that can set environmental policies
for this company, right?
A. No, I didn't say that. Q. I thought you told me that.
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A. No, I think I was pretty clear that I am a
member and I can recommend policy.
I didn't say that I
could set policy.
Q. You could recommend as a policy that Solutia
take whatever course is necessary to get these fish
advisories taken off of the river system, right, you
could recommend that?
MR. PECK:
Object to the form of the question.
No foundation.
THE WITNESS:
I guess on a speculative basis.
I don't know how to answer the question.
BY MR. GRAMMAS:
Q. Well, answer the question as best as you can,
given your understanding of your job responsibilities.
Could you go up tomorrow and write a memo -- who would
you write a memo to if you would wanted to enact some
new policies, environmental policies?
A. It would go to our policy committee, corporate
policy committee.
Q. And who all's on that committee?
A. Again, I think I said it's Mr. Potter, Mr.
Hunter, and there are a few others that -- again, I
don't know the current listing of those folks.
Q. All right. Whoever these people may be, sir,
you could go to your office in the morning and dictate
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_______________________________________________________________ ________________ _____
a memo to these people that says, As the head
environmental manager over health and safety, I believe
Solutia should embark on a course of conduct to do
whatever it takes to get fish advisories removed from
Choccolocco Creek and Lake Logan Martin.
A. I could do that if I felt that that was
appropriate and necessary to do and it was our
responsibility to do that, yes.
MR. GRAMMAS:
That's all the questions I have.
Thank you.
(DEPOSITION ADJOURNED)
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23:
STATE OF MISSOURI COUNTY OF ST. LOUIS
) ) )
I, KEVIN J. WEICHMAN, CSR, RPR, Notary Public in and for the County of St. Louis, State of Missouri,
do hereby certify that pursuant to stipulation there
appeared before me on the 28th day of October, 1998,
Taylor & Schroeder Reporting & Video, 7494 Ethel
Avenue, St. Louis, Missouri, MICHAEL PIERLE, who was
first duly sworn by me to testify to the whole truth of his knowledge touching the matter in controversy
aforesaid, so far as he should be interrogated
concerning the same; that he was examined and the
examination was taken down in shorthand by me and
afterwards transcribed by computer-aided transcription.
IN WITNESS WHEREOF, I have hereunto set my hand and affixed my notarial seal on this 28th day of
October, 1998.
KEVIN J. WEICHMAN, CSR/RPR Notary Public
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____ --_____________________________________________ _____________________233
STATE OF MISSOURI COUNTY OF ST. LOUIS
) ) )
I, MICHAEL PIERLE, do hereby certify:
That I have read the foregoing deposition;
That I have made such changes in form and/or
substance to the within deposition as might be
necessary to render the same true and correct;
That having made such changes thereon, I
hereby subscribe my name to the deposition.
I declare under penalty of perjury that the
foregoing is true and correct.
Executed this day of , 1998, at , .
MICHAEL PIERLE
Subscribed and sworn before me this of , 1998.
day
My Commission Expires:
Notary Public
TAYLOR * SCHROEDER REPORTING & VIDEO
(314) 644-2191
WATER PCB-SD0000021235
1 2 3 4 5 6 7 8 9 10 11
12
13 14 15 16 17 18 19
20 21 22
23 24 25
234
DEPOSITION CORRECTION SHEET DEPONENT: MICHAEL PIERLE
RE:
THOMAS C. DYER, ET AL vs. MONSANTO COMPANY,
Consolidated For Discovery With SHELTER COVE
ET AL
MANAGEMENT, INC., ET AL vs. MONSANTO COMPANY, ET AL
Upon reading the deposition and before thereto, I would like to indicate that changes should be made:
subscribing the following
Pacre Should Reason
Line read assigned
for
chancre :
Pacre Should Reason
Line read assigned
for
chancre :
Pacre Should Reason
Line read assigned
for
chancre :
Pacre Should Reason
Line read assigned
for
chancre :
Page Should Reason
Line read assigned
for
chancre :
Paqe Should Reason
Line read assigned
for
chancre :
Page Should Reason
Line read assigned
for
chancre :
Page Should Reason
Line read assigned
for
change:
SIGNATURE OF DEPONENT: DATE:
TAYLOR * SCHROEDER REPORTING & VIDEO
(314) 644-2191
WATER PCB-SD0000021236
Michatjj! A. Pierle Vice President of Environment, Safety and Health http://www.soIutia.com/Corporate/CorporateOfflcers/MichaelPierle.htm ' LU
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Michael A. Pierle
Michael A. Pierle is a Vice President of Solutia Inc. with responsibility for environment, safety and health. He assumed his present position on Sept. 1, 1997. In this new position, he continues to hold the responsibilities of the position he previously held since April 1991, as Monsanto Company's Vice President, Environment, Safety and Health. These include: issue identification and management, development of policy initiatives, compliance oversight of both internal and external requirements in the areas of environment and worker and community health and safety.
Mr. Pierle joined Monsanto in 1966 in environmental engineering and worked in a variety of areas ranging from energy conservation programs to the environmental control management over the next eight years. In 1974-1975, he was on leave to work for the Department of Commerce in their Office of Environmental Affairs.
In 1975, Mr. Pierle was named Manager of Environmental Protection for the Monsanto Industrial Chemical Company. In the following year, he became the Manager of Environmental and Energy Affairs of the Monsanto Chemical Intermediates Company. In 1979, he was appointed Regulatory Management Director-Water for Monsanto Company and Director of Regulatory Management-Hazardous Waste in 1983. In 1984, he was appointed Director of Environmental Management for Monsanto Company.
In 1986, he was named Director of Environmental Operation of Monsanto Chemical Company, an operating unit of Monsanto Company, with responsibilities for implementing compliance programs, cleanup of Superfund sites and managing product safety and approval programs.
Mr. Pierle is on the Board of Directors of the Chemical Industry Institute of Toxicology (CUT), The American Eung Association of Eastern Missouri and The Monsanto Fund. He is Chairman of the National Wildlife Federation's Corporate Conversation Council. He also serves on the Advisory Committee of the Purdue University School of Engineering and Washington University School of Engineering and Applied Science.
Mr. Pierle received a B.S. degree in civil engineering from Purdue University in 1966. He then received his M.S. in environmental engineering in 1971 from Washington University. In 1983, he attended the advanced management program at the University of Texas. Mr. Pierle completed the Stanford Executive Program in 1990. He is a licensed
10/25/98 12:24 PM
WATER PCB-SD0000021237
Michael A. Pierle Vice President of Environment, Safety and Health http://www.solutia.com/Corporate/CorporateOfflcers/MichaelPierle.htm
professional engineer.
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Copyright 1998 Solutia Inc. All rights reserved. Retransmission, reproduction or distribution without express written permission ofSolutia Inc. is prohibited. Solutia and
the Solutia logo are trademarks ofSolutia Inc.
2 of 2
10/25/98 12:24 PM
WATER PCB-SD0000021238
NEWS __
for RELEASE
IMMEDIATELY 1970
fASHrarmw, o. c. SAIT PICKARD
19*
Pc
Monsanto
E. V. John (314) 694-2891 0PUBLIC BLATIONS PAPTM{MT WomiRt# Compiny
100 N. Cln<kr|h Si. UvIi. Missouri 13116
MONSANTO CITES ACTIONS TAKEN ON ENVIRONMENTAL ISSUE
ST. LOUIS, July 16 -- Monsanto Company, sole U.S. producer of an industrial chemical called polychlorinated biphenyl (PCB), today said recent political charges and sensational headlines about the chemical causing "a major ecological crisis" completely Ignore voluntary actions the company has taken to restrict use of the material.
"Our program began back In 1968 with the proper identification and measurement of PCB in the environment and will conclude this year by our unilateral action to restrict Its use," Howard L. Minckler, company vice president and general manager of its Organic Chemicals Division, said.
He added that Monsanto had not been pressured into % action by any legislation or organized group. "We have taken decisive action based on evidence that PCB is a persistent chemical which builds up in the environment."
-more-
DSW 019301
*
WATER PCB-SD0000021239
' '
)
--2 MONSANTO: MINCKLER'S REPLY TO PCB CHARGES xxx environment."
Commenting on a recent report that PCB can induce birth defects In animalsMlnckler said, "Monsanto Is not aware of any scientific data that indicates polychlorinated biphenyls may cause birth defects. The results of comprehensive toxicity
i studies, sponsored by Monsanto and using the usual species of laboratory animals, have failed to produce such effects^
"Scare tactics and sensational reporting do not serve the public interest nor solve ecological problems," he said. "Only a few reports have stated why PCBs were ever developed and why they are used today. Nor have the consequences of not using PCB been explained.
"What should be emphasized," Minckler continued, "is that PCB was developed over 40 years ago primarily for use as a coolant in electrical transformers and capacitors. It is also used in commercial heating and cooling systems. It is not a 'household* item.
"Anyone who lives in a large city is familiar with power failures. During periods of peak power needs, air conditioning and refrigeration fail, lights go out and commuters are stranded. If power companies were to remove PCB from equipment, we have been told that major blackouts would occur throughout the world.
-more-
DSW 019302
WATER PCB-SD0000021240
I)
--3 MONSANTO: MINCKLER*S REPLY TO PCB CHARGES xxx world.
"PCB la used In electrical equipment as a safety
fluid. It has replaced combustible oil products which have,
on many occasions, exploded and burned, causing deaths and
injury to human life. Today state and local laws all over the
country require Che use of non-flammable fluids in certain
electrical equipment as a safety feature. At the moment, there
are no substitutes available which equal the safety performance
of PCB."
Monsanto said it intends to continue selling PCB for
"closed-system" uaea such as electrical components and
heat-transfer systems. "With rigid control over where the
product goes, how it is handled and disposed of, we believe the
safety functions of the product can continue to serve society
and the environment can be protected," Minckler said. "We are
discontinuing sales into 'open systems' -- adhesives, sealants,
chlorinated rubber, specialty paints, etc.
"For other uses, such as fire-resistant hydraulic
fluids, wtiere PCB cannot be strictly controlled, we have
reformulated some fluids and they are on the market. The new
products contain other fire-resistant ingredients. We will
continue to develop alternate formulations which do not contain
persistent PCB. We will not abandon hydraulic fluid users,"
Minckler commented, "as has been reported." -more-
OSW 019303
*
WATER PCB-SD0000021241
I
--4 MONSANTO: MINCKLER'S REPLY TO PCB CHARGE xxx reported."
Monsanto has also- established a new system for disposal
or recycle of spent PCB. A special high-temperature incinerator
will break down PCB into harmless materials. The company also i
regenerates spent fluids for reuse. The incinerator will be
offered to customers who cannot otherwise destroy or regenerate
their old fluids.
"Although loss of PCB from our manufacturing plants
has been negligible, we have further tightened up our production
techniques and installed new pollution abatement devices," the
Monsanto executive said.
...................
"I repeat," Minckler concluded, "our program was
initiated and conducted by Monsanto alone. It will be concluded
this year. We believe it is a position any responsible company
would take."
-0O0-OS
OS W 019304
*
WATER_PCB-SD0000021242
r o. - Monsanto Pledge SUN Oulhu I C 01/" ti1 UNITY INFORMATION
C DlViikLMMJUSKS
http://www.solutia.com/Community/MonsantoPledge.htn SO LU 7 I A Itw
f n?uT
\ i!>:.<: pH-
|
Ulj&dL- -
home Site map feedback Search
Monsanto Pledge
The Monsanto Pledge was announced by Chairman and CEO Richard J. Mahoney at a meeting of the Corporate Conservation Council of the National Wildlife Federation in Washington, D.C., on Jan. 30, 1990. Here is the pledge as announced by Mahoney:
"It is our pledge to reduce all toxic and hazardous releases and emissions, working toward an ultimate goal of zero effect. It may take time, but we will not be satisfied with anything else.
"It is our pledge to ensure that no Monsanto operation poses any undue risk to our employees and our communities.
"It is our pledge to work to achieve sustainable agriculture with the lowest inputs feasible, through new technology and new practices.
"It is our pledge to ensure the safety of groundwater. If our products are found to pose a problem, we will solve it by whatever means necesssary. We will make our technical resources available to farmers who may have concerns about groundwater contamination, even if none of our products is involved.
"It is our pledge to keep our plants open to our communities, bringing the community into plant operations. Our employees and our communities will be kept fully informed of any significant hazard - if we can't eliminate the hazard, we'll work to eliminate the source of it.
"It is our pledge to do our part to halt deforestation and declining biodiversity. All corporate real estate, including plant sites, will be managed with the benefit of nature as a serious operating factor.
"It is our pledge to search worldwide for technology that will reduce and eliminate waste from our operations, with the top priority being not making it in the first place.
"Our commitment is to achieve sustainable development for those aspects of the environment where we have an impact. Our commitment is to
9/9/98 9:17 AM
WATER PCB-SD0000021243
Sclutla <nn. - Monsanto Pledge
http://www.solutia.com/Comrnunity/MonsantoPledge.hti
achieve sustainable development for the good of all people in both developed and less-developed nations.
"But it is not enough to simply 'unpollute' the world. We must provide food and energy for ever-growing populations, most of which are in the Third World and not in the developed nations, which have the resources and freedom to worry about these vital environmental issues.
'We must rectify the mistakes of the past while we continue to develop and introduce the new technologies to provide the essentials for mankind in the future.
"And we must ensure, as we know we can, that these new technologies will not create problems to be dealth with by our children, grandchildren, and great-grandchildren.
"I have described the Monsanto Pledge. We are determined to achieve it and we are pursuing the programs needed to achieve it."
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9/9/98 9:17 At
WATE R..PC B S D0000021244..
So'utia me. - Environmental Commitments
http://www.solutia.com/Community/EnvironmentalCommitments.htrr
home Site Map Feedback Search
Solutia's Commitments to Environment, Mpp*" Safety & Health
MlinTppf?
Solutia's Environmental, Safety & Health Commitments are based on our strong convictions that continuous improvement in these areas is critical to creating value for all stakeholders. These commitments are drivers for a better future.
We will ensure that our operations and distribution systems are safe for our employees, site contractors and guests, communities and the environment.
We will make products that are safe when used responsibly.
We will keep our operations open to our communities, and foster open communications with all of our stakeholders.
We will continuously improve our raw material and energy utilization efficiencies to reduce our impact on the environment and improve the sustainability of our businesses.
We will encourage active participation in and positive contributions to safety, health, and environmental stewardship by our employees.
We will search worldwide for new technologies that bring environmental, safety and health value to all of our stakeholders.
9/9/98 9:53 AM
WATER PCB-SD0000021245
Goiuiia i.ic. - Environmental Commitments
http://vww.solutia.com/Community/EnvironmentalCommitments ht
Solutia People Talk About the Commitments Background on Solutia's ES&H Heritage
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Solutia and the Solutia logo are trademarks of Solutia Inc.
2 of 2
9/9/98 9:53 Al
WATER PCB-SD0000021246
n ec eivz
ussy
UNITED STATES ENVIRONMENTAL PROTECTION AGENCY Ci C 2 9 19,
WASHINGTON. D.C. 20460
J.1-. K.
December 22, 1975
OrriCl O' Tut
ADMINIJDUIoe
Dear Mr.
Tor at least five year*, the Federal Government and the nenufsecuring industry have been aw.re that polychlorinated biphenyl. (ICBiTpiiM a -wTflT tg hum htath^and-the-anvirotaant. Last month, at EPA's National Conference on rolychiuiiiiilid Blplieujls in Lhluage, - leading experts dearly doeuaaneed the fact that PCS. are pervasive in the environment,arecsue ing disruption and economic ham to___ commercial fishing in many areas and are creating a serious potential health hasard to the public. While certain voluntary measures have been initiated in the past, the widespread and persistent occurrence '
-of^PCis-nnaerjlWsa^the-failureroljvxistlat-practlcea.-to-adeauacelr
control fill BILI
I Today Z announced a broad EPA program of regulatory and nonregulatory actions to reduce the levels of PCBa in the environment. My statement, (which is endoaed), stated that ve must, as a soeiaty,
accept and work toward a goal of totally eliminating the production, l importation and use of FCBs as rapidly as possible. Toward that end,
X am asking you, as a prindpal aaaber of the PCS Industry, to commit TrTf to m deliberate and expeditious search for dtematives.
dtematives will be required, the economic aspects of turn changeover :
I will have to be considered. Z dso recognize that such an effort cannot be eceoapliahed overnight. Nevercheleas, Z have confidence that American industry has the capacity to aolve this difficult task,
I and 1 solicit your full cooperation and participation in this effort.
go thee ve eaa begin this undertaking as soon as possible, Z am inviting you and other representatives of your industry to meet with
I me am January Id to discuss this undertaking end work eowards the dsvslopmsnt of plans on bow it can be accomplished as smoothly and rapidly as possible.
i Z have also asksd representatives of the principal users of PCBconealning transformers and large capadters to meet vleh me on January 22 to discuss ways that ve eaa effectively manage and conerol FCBs in current use. X am enclosing a copy of'ey lector to these
i companies. At our meeting on January 14, wo slight also discuso some of the suteere outlined in that letter.
OS* 012433
WATER PCB-SD0000021247
n
'
1,4 #/ard to seating with you at EPA in *oom 1112.
I .. looking
; crystal Hall 02, Arlington, Virginia, on
1921
^ "SuZ Inthm afternoon. If you ha*. any
January 1*. fro. two to^ arringenent# f,, thi. meeting. you may
questions concerning
<.. 7S5-AQ56
contact Dr. I. E. Wallen, (202) 755 6956.
^Sincerely youra,
IVrAAJl 2. //uu^
Hus sell E. Train
AdainiatTator
Hr. John W. Hanley
Preaident Honaanto Chemical Company 800 N. Lindbergh Boulevard Bt. Louia, Hiaaouri 63166
.............................. .
.
'
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OSW 012434
WATER PCB-SD0000021248
IN THE 3 OTH JUDICIAL CIRCUIT' COURT FOR ST. CLAIR COUNTY, ALABAMA PELL CITY DIVISION
THOMAS C. DYER, ET AL, Plaintiff
vs . MONSANTO COMPANY, ET AL,
Defendant
) ) ) .) ) ) -) ) )
.
NO.
CV-93-250
. '*
,
i
Consolidated For Discovery With
SHELTER COVE MANAGEMENT, INC., ET AL,
Plaintiff, vs . MONSANTO COMPANY, ET AL,
Defendant
)' ) ) ) ), ) NO. CV 94-50-PH ) ) ) )
DEPOSITION OF MICHAEL A. PIERLE Taken on behalf of the Plaintiff
October 28, 1998
REPORTER:
Kevin J. Weichman, CSR-RPR No. 084-003189
DbpoNet
Taylor * Schroeder Reporting & Video
"Meeting All Your Litigation Needs
COURT REPORTERS
7494 Ethel Avenue St. Louis, Mo 631 17 314.644.2191 800.280.DEPO Fax 314.644.1334
quality
ASSURANCE
WATER PCB-SD0000021249
SOLUTIA COMMITMENTS
MANUAL
<DRAFT>
June 9,1998
DSW 122270
WATER_PCB-SD0000021250
1 ADLL u r
CONTENTS
1222^
DSU
WATER PCB-SD0000021251
TABLE OF CONTENTS
I. INTRODUCTION - THE SOLUTIA COMMITMENTS
II. GENERAL
1. Internal Global Environmental, Safety, and Health (ESH)
Requirements Setting Procedure (to be written)
2. Chemical Distribution 0
3. Outside Processors '
4. Community Awareness at Manufacturing Sites
5. Environmental, Safety and Health Reviews of Capital Projects /
6. Environmental Safety and Health Reviews of Divestitures or Acquisitions of Property and/or Businesses (to be written)
AQ*
7. Environmental, Safety and Health Protection for Investments
Over Which the Company Does Not Have Operating Control
(to be writtenjnzr \ i :__f~\ i , ,_n______ ,.
8. Environmental, SafetyrHealthl and OccupationaiMedicine
C,,ompliance AL ud,iitJinig i \i ii_j--\iUi
jU| r^--'
. m. ENVIRONMENTAL
1. Pollution Prevention 2. Groundwater and Soil Quality 3. Ozone-Depleting Chemicals (CFCs)
IV. SAFETY
L Safety Management Process 2. General Requirements 3. Tiered Requirements/Hazard Levels 4. Variance Procedure 5. Safety Guidance Documents
OSH 1222-72
WATER_PCB-SD0000021252
V. HEALTH
X. Industrial Hygiene Management Process 2. General Requirements 3. Tiered Requirements/Hazard Levels 4. Variance Procedure 5. IH Guidance Documents
i
VI. PRODUCT STEWARDSHIP
1. Product Stewardship
2. Premanufacture Notification to the United States
Environmental Protection Agency Under the Toxic Substances
Control Act
3. Recording Allegations of Significant Adverse Reactions Under
the Toxic Substances Control Act
'
4. Transmittal to the United States Environmental Protection
Agency of Substantial Risk Information Under the Toxic
Substances Control Act
5. Transmittal ofToxicology and Healtlritelated Data to United
States Regulatory Agencies/ \ j |--J
6. Use of Animats-in^ReseardrPacilities
VH. OCCUPATIONAL MEDICINE
Insert Occupational Medicine section here
VHI. CROSS-REFERENCE: Commitments Manual and Responsible Care (to be written)
IX. REFERENCE: Responsible Care Program
filename:tbcon.doc (in Nepran M-private) rev. 6/8/98 2
J3SW 12Z273 WATER PCB-SD0000021253
DSW 122274
I
WATER PCB-SD0000021254
introduction
The Solatia Commitments
Solutia Inc. is dedicated to ensuring the safety of our employees, customers, communities and the environment Through the Solutia Commitments, we are publicly obligated to pursue a course of stewardship that goes beyond what is required by the law. This ideal is best described in a memo issued jointly by Bob Potter and John Hunter on March S, 1998. It is as follows:
Solutia's Commitments to the Environment, Safety & Health
Even before we began operating as our own company, we knew that stewardshipfor the environment, safety and health was critical to our long term success. That's why one ofourfive business imperatives is "Being a responsible company that operates safely, with respectfor the environment and the communities in which we do business. "
Notice that we called this a business imperative. Our rich heritage in ES&H stewardship as well as ourparticipation in the Responsible Care program of the Chemical Manufacturers Association, has taught us that taking care of the environment, our own people's health and safety, and the safety of6ur communities is basic to earning the public's right-to-operate, and basic to our long-term business success.
To support ourbusiness-imperatives, weJurve-develeped what we 're calling
Solutia's..Cgmmitrhents tpjheiEnvirpnmentJSafety & Health. These
commitments', were]developed,by Solutia people, and approved by our Executive
ManagehtentiTeam/and-the Boapd ofEHrectors. L-J C^"
Our Commitments are based on our strong convictions that continuous improvement in these areas is critical to creating valuefor all ofour stakeholders. These Commitments are driversfor a betterfuture:
We will ensure that our operations and distribution systems are safefor our employees, site contractors and guests, communities and the environment
We will make products that are safe when used responsibly.
- We will keep our operations open to our communities, andfoster open communications with all ofour stakeholders.
We will continuously improve our raw material and energy utilization efficiencies to reduce our impact on the environment and improve the sustainability ofour businesses.
We will encourage active participation in andpositive contributions to safety, health, and environmental stewardship by our employees.
1-1 DSW L222 75
WATER PCB-SD0000021255
We will search worldwidefor new technologies that bring environmental safety and health value to all ofour stakeholders.
... We're asking each ofyoufor yourfull supportfor andfull participation in our Commitments to ES&H and Responsible Care. They are more than nicesounding statements; they represent who we are as a company.
Bob Potter Chairman and CEO
John Hunter President and COO
!
\
D) /a\
-------- \r~
l
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n i /^A U Li i--1 \_i
J
1-2 OSW .122276
WATER PCB-SD0000021256
THE SOLUTIA COMMITMENTS
We will ensure that our operations and distribution systems are safefor our employees, site contractors and guests, communities and the environment
We will make products that are safe when used responsibly.
We will keep our operations open to our communities, and foster open communications with all ofour stakeholders.
| ,--N'\ j -^\ /7\ | (-----II--. |--;
We will continuously *improve/qur^ raw-maierialand energy utilization efficiencies1^reduce~QMr5mpa/k arithe environment and improve the sustainability ofour businesses. ....
We will encourage active participation in andpositive contributions to safety, health, and environmental stewardship by our employees.
We wiU seatch worldwide for new technologies that bring environmental, safety and health value to all ofour stakeholders.
fiiename:solint2.doc (in Nepran M-private) 1-3
OSM 122277
WATER PCB-SD0000021257
DSW 122278
WATER_PCB-SD0000021258
Program GEN6 ENVIRONMENTAL, SAFETY AND HEALTH REVIEWS OF DIVESTITURES OR ACQUISITIONS
OF PROPERTY AND/OR BUSINESSES (to be written)
fllename:divacq.doc (in Nepran M-private) rev. 6/9/98
DSW 122213
WATER PCB-SD0000021259
Program GEN7 ENVIRONMENTAL, SAFETY AND HEALTH PROTECTION FOR INVESTMENTS OVER WHICH THE COMPANY DOES NOT HAVE OPERATING
CONTROL (to be written)
fllename:nocontr.doc (in Nepran M-private) rev. 6/9/98
osw . 122280 WATER PCB-SD0000021260
Program GEN8 Environmental, Safety and Health Compliance Auditing
OVERVIEW
Introduction
This program describes the auditing policy and procedures to be taken to confirm that site management systems are in place to ensure continuous improvement and compliance with government regulations and company, business unit and subsidiary policies and procedures.
Policy
The company will conduct environmental, safety and health compliance audits to confirm that site management systems are in place to ensure continuous improvement and compliance with both government regulations and company, business unit and subsidiary policies and procedures.
For Further Information
'
When further information or clarification is required, you may contact the following:
ISSUE OWNER: Garth Fort, Leader, ESH Policy & Compliance, F2EI (314)674-8886 .
TECHNICAL CONTACTS: '---- / \ j 1 | | :-----"J j /"^ \
SAFET^AND iPRGP^TprTOOTECTIO^ \ H. D. (Dunriy) ToyrESH Policy Ar&nnpliartce, (314)674-6698
INDUSTRIAL HYGIENE H. D. (Dunny) Toy, ESH Policy & Compliance, F2EI (314)674-6698
OCCUPATIONAL MEDICINE David C. Shepperly, Soluda Medical Director, F2EF (314) 674-7862
ENVIRONMENTAL COMPLIANCE Neil E. Prange, ESH Policy & Compliance, F2EI (314)674-6740
Program Approval
The content of this program was approved by
P17-1
JDSW 122261
COMPANY CONFIDENTIAL
WATER PCB-SD0000021261
PI 7.1 PROCEDURES
P17.1.1 Introduction
P17.1.2 Standard
This section describes the procedures to be used in ESH Compliance Auditing.
Each business unit and subsidiary will be responsible for ensuring that audits are conducted in accordance with criteria shown in the following table:
ESH Compliance _
-
will.
Auditing Programs Auditors
be consistent with the five-step auditing approach as outlined by the outside consulting firm of Arthur D. Little, and
follow protocols approved by the Leader, ESH Policy & Compliance
be appropriately trained, knowledgeable of the subject they
audit, and skilled as compliance auditors, and
-
be independent of the Iocation/site they audit
P17.1.3 Audit Frequency
ESH compliance audits will be performed on a three-to-five year maximum cycle. Frequency for each site will be reviewed by Policy/Planning Team and will depend upon
results ofrhe last Audit] 1 'j } / a \
dje--g---reI eiof1"risk, j complexity,! and-' / compliance issues.
/ l\ \
11 Z/A u
P17.1.4 Audit Reviews
Reports of the actual audit findings and/or recommendations will be reviewed by appropriate legal staff and distributed, at a minimum, to
site managers,
directors of manufacturing (or equivalent for non-manufacturing locations),
legal,
ESH Leader,
.
Leader, ESH Policy & Compliance, and
Operational Excellence Process Leader.
P17.1.5 FoDowup
Audit findings/recommendations followup will be the responsibility of each business unit and subsidiary.
The Leader, ESH Policy & Compliance will request periodic status reports of auditing and followup corrective actions for communication to upper management.
filename:sol 17neo.doc fin Neman M-public) rev. 6/9/98
P17-2
OSW 122282
COMPANY CONFIDENTIAL
WATER PCB-SD0000021262
Program GEN1 INTERNAL GLOBAL ENVIRONMENTAL, SAFETY,
AND HEALTH (ESH) REQUIREMENTS SETTING PROCEDURE (to be written)
j i'a\
filename:reqsetddc (in Nepran M-private) rey.6/9/98
DSW L2228J
WATER PCB-SD0000021263
OVERVIEW
Program GEN2 Chemical Distribution
Introduction
Policy Goals
Measuring Progress For Further Information
This program describes the policies, goals, standards and procedures necessary to implement Solutia's commitment to "... ensure that our operations and distribution systems are safefor our employees, site contractors, communities and the environment. '
The company will reduce the potential risk to its employees, the public, carriers, distributors, contractors, customers' employees and the environment in the distribution of chemicals.
Business units must work toward incident-free performance in the distribution of chemicals, including
raw materials, intermediates, finished products, byproducts, and wastes.
.
Appropriatejneasureinertt systems will ensure continuous improvement toward stated goals and
objectives.''''" I !
Ji j! i
-- ** ! 1i
l/\
/
\
i ---- '
II
"''O>'T-.
When further information or clarification is required, you may contact the following;
ISSUE OWNER David E. Williams, Supply Chain, F2WI (314)674-8644
Program Approval
The content of this program was approved by
In This Program This program contains the following procedures.
Procedures
P5.1 INCIDENT REDUCTION P5.2 SAFETY STANDARDS FOR WAREHOUSES AND
TERMINALS
See Page P5-2 P5-5
OSW 122284
P5-1 COMPANY CONFIDENTIAL
WATER PCB-SD0000021264
P5.1 INCIDENT REDUCTION
P5.1.1 Introduction mil Definition
P5.1J Actions
This section describes procedures used to accomplish the company's specific goals for incident reduction in chemical distribution in order to effect incident-ffee performance.
An incident is defined as any undesirable event occurring during a chemical distribution process over which the company has direct control or influence that results in
aninjury, an unintentional release of a chemical, and/or damage to property or the environment.
'
To achieve the goal of incident-free performance, the company will
improve the carrier selection process to identify and contract transportation services with carriers who consistently demonstrate safe performance in the movement of the company's chemical products,
improve the safety of chemical transportation practices through application of continuous improvement concepts,
develop and apply technological advancements to improve chemical distribution safety and share these with the industry as appropriate.
provide technical advice and'assistance through itsTmergency response system in a
-Auresponsible arid timely [manner for /butside planLgate" incident-involving its chemical
products. l_L u
measure and continuously improve its response capabilities, and
have trained personnel physically present, in an expeditious manner, at the emergency site
- upon request of the local emergency responder or public official, or
--^ --
- when the company feels a qualified emergency team can lessen the severity of an
incident or ease a community's concerns about the company's products.
Continued on next page
-DSW 122285
P5-2 COMPANY CONFIDENTIAL
WATER PCB-SD0000021265
P5.1 INCIDENT REDUCTION, Continued
P5.1.4
The company's effort to effect incident-free performance will include the emphasis areas shown
Emphasis Areas below.
Emphasis Area
Details
Emergency Response Each shipping location will have a current plan for responding to chemical transportation emergencies involving products/materials within its scope.
The locations' emergency responders will receive regular training that meets or exceeds regulatory or industry standards.
Training history for all emergency response personnel will be documented.
Partnerships with local communities & local emergency responders along chemical transportation routes, as well as in those communities where its chemical plants are located, will be encouraged. .
The total emergency response plan will be continuously monitored and improved.
Detailed post-incident reports and preventive action plans will be provided as training aids to all emergency responders.
Community-------- . Awareness^. ;--\N
__ Community-outreach programs will,be supported by offering
plant facilities\and mutualTramngTo,,emergency responders in
^ommunitiesjjeighbonne the compahy&distribution network.
Through routine .conununicationiwith the public, continuous
1-- improvement iirsafexhemical distribution will be emphasized
and public concerns will receive response.
Trained plant employees-will be the company's."ambassadors''
to the community to convey company progress and commitment
to improving the safety of chemical distribution and the
___
effectiveness of its emergency preparedness and response.
Continued on next page
Ds* 122286 P5-3 COMPANY CONFIDENTIAL
WATER PCB-SD0000021266
P5.1 INCIDENT REDUCTION, Continued
P5.1.4
`
Emphasis Areas
Emphasis Area .
Details
Risk Assessment Compliance Adding Value
Distribution accidents/incidents and any resulting loss of
containment will be reduced according to a documented
distribution risk management methodology.
-
An initial qualitative risk assessment methodology will be made
available for use.
Quantitative risk assessment models will be evaluated for
especially sensitive materials.
Regulatory changes that affect the distribution of the company's products will be monitored and changes will be communicated to shipping locations.
Compliance audits and training will be conducted at all company shipping locations as appropriate and reported annually.
The company will recognize, as appropriate, the potential for adding value to it products.
| *--N'\
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i
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OSW . L222a7 P5-4 COMPANY CONFIDENTIAL
WATER PCB-SD0000021267
P5.2 SAFETY STANDARDS FOR WAREHOUSES AND TERMINALS
P5.2.1 Introduction
This section describes the procedures used to accomplish the company's specific goals for incident reduction in chemical distribution in order to effect incident-free performance as related to warehouses and terminals that receive the company's products.
pg j ? Standards
To extend a seamless policy of operating safety results to warehouses and terminals that receive
the company's products, the following standards, comparable to the company's, will be
incorporated.
~
Precontracting requirements will be used to assess firms that can handle the company's products in a manner that is safe for its employees, the public and the environment
Information on the company's policies, procedures and requirements regarding the safe handling and transportation of chemicals will be provided to warehouse and terminal personnel.
Continuous improvement concepts will be applied to all aspects of contract management for improvement in safety and reliability of provided-services.
Agreed-upon performance measurements and periodic reviews will be used as indicators of progress toward zero-incident status.
P5JL3 Emphasis Areas
The recognition of public concerns about emergency preparedness and safe distribution
practices will be-e*tended-te-ail the company's distribution-locations.
^ i - \ \ \ ii i a \ 1 i--
ii
S.\ !
!iI
1 / ___ \ | !
t|
J
The compands efforTtp-cxtend a seamless policy_of operadngjafetjCxesults to warehouses and
terminals that will receive the company's products will include the emphasis areas shown
below.
Emphasis Area
Details
^
Selection Criteria
Documented selection criteria that include appropriate safety measures will be maintained.
Information Flows
Defined flows of information concerning company policies, procedures and requirements on the safe handling of its products will be maintained.
Performance Reviews
Reviews of performance against company requirements will be conducted on a specified review cycle.
Risk Management Risk management and emergency preparedness activities will be supported at all the company's distribution locations.
filenamc:sol5.doc fin Neoran M-publicI rev. 6/9/98
os* 122Z88
P5-5 COMPANY CONFIDENTIAL
WATER_PCB-SD0000021268
OVERVIEW
Program GEN3 Outside Processors
Introduction
This program describes policies, goals, standards and procedures necessary to implement Solutia's commitment to . ensure that our operations and distribution systems are safefor employees, site contractors, communities and the environment. "
Policy
To support its operations, the company will select outside processors that will operate with concern for
worker safety, regulatory compliance, community protection, and protection of the environment
Goal
Measuring Progress
The company will pursue into its outside processor plan the specific goal to manage the
company's exposure to present and future liabilities associated with the use of outside
processors by maintaining currentassessments and written-contracts for each outside processor
used.
^
1
/A\ ! >\ \
Ii
To measunr^ogcesaaghinsuhis grtaf. the company will maintain records that document the
outside processors used, status of assessments, and status of contracts.
For Further Information
.
When further information or clarification is required, you may contact the following:
ISSUE OWNER H. D. (Dunny) Toy, Policy & Compliance, F2EI (314)674-6698
Program Approval
The content of this program was approved by .
Continued on next page
-OSH 122-289
P7-1 COMPANY CONFIDENTIAL
WATER PCB-SD0000021269
OVERVIEW, Continued
In This Program This program contains the following procedures. Procedures
P7.1 OUTSIDE PROCESSORS P7.? TOLL MANUFACTURERS
SeePage
P7-3 P7-4
DSW 122290
P7-2 COMPANY CONFIDENTIAL
WATER PCB-SD0000021270
P7.1 OUTSIDE PROCESSORS
P7.1.1 Introduction
This section describes procedures to be used to accomplish the company's specific goals
regarding outside processors.
.
P7.1J Applicability
This section applies to firms which provide services related to Soiutia chemicals, products or wastes. This includes toll manufacturers, which are a subset of Outside Processors and which are detailed in the next section of this chapter.
P7.1.3 Selection Elements
The company will use only outside processors that have been selected and periodically assessed to ensure their
ability to protect the public, employees and the environment adequately from any adverse effect of the.company's chemicals, products or wastes,
compliance with all applicable laws and regulations,
knowledge of potential hazards and any applicable manufacturing requirements associated with the handling of company materials, and
use of waste disposal methods and locations as specified by contracts, with recordkeeping of all material use and waste disposal.
P7.1.4 Assessments
Before they are usedby^thc-company, outside processors .will-bc-subjcct to
contractor ; ) } IT*' / \ \ on-site^assessments^tnless waived (see-7. I\6, Waivers),
fal'by'tfnrappropriate Directw of Manufacturing orequivafent, and approvals and reviews by others as appropriate.
NOTE: The Leader, ESH Policy & Compliance co-approves selection of waste management
firms, including cleaning firms.
. __,
P7.1.5 Assessment Requirements
Initial assessments are intended to be thorough and multi-disciplinary. Periodic reassessments will concentrate on general performance and deficiencies previously defined.
P7.1.6 Waivers
On-site assessments of outside processors are required unless waived by both the Leader, ESH Policy & Compliance and the Director of Manufacturing and formally documented. Any such waivers must be resolved or re-approved every three years or less.
P7.1.7 Waste Management
For outside processor categories other than toll manufacturing (waste management, cleaning services, etc.), a processor's waste management practices will be reviewed as part of the on-site assessment
P7.1 OUTSIDE PROCESSORS, Continued
Continued on next page L2229LI
P7-3 COMPANY CONFIDENTIAL
WATER PCB-SD0000021271
P7.1.8 Worldwide
Applicability
These elements will be implemented worldwide, with modifications to reflect local conditions
and the extent of the company's operating control.
.
OSH - 1222-92
P7-4 COMPANY CONFIDENTIAL
WATER PCB-SD0000021272
P7.2 TOLL MANUFACTURERS
P7J.1 Introduction
This section describes procedures to be used to accomplish the company's specific goals regarding toll manufacturers.
njj.
Applicability
This section applies to toll manufacturers, which are firms under arrangements where Solutia owns two or more of the following factors:
raw materials, process technology, or some or all of the output.
.
.
Pilot plant operations for process development and/or market introduction are included.
P7.2J Accountability
P7.2.4 Selection Elements
The Director of Manufacturing is the primary person accountable for ensuring that the initial assessments, contracts and other provisions are in place prior to commencing operations.
Approval must be based on the assessment and any waivers (see 7.2.10, Waivers).
The Director ofManufacturing will consult as needed with business and environmental management
The decision to toll will be reviewed and re-approved by the Director of Manufacturing, or
equivalent, at least every three years.
.
^--1
\ \ I : I , / A \ ! I ____
II
In additjcrtCkrthe selection IcIeBRints listed for, outside processors, theemnpany will use only
toll manuihcturersJhaf Ipavebeeni seletted-ancfperiodically atssessetUo^ensure their
'
ability to produce to market demands, producing quality product cost-effectively,
capability to manage key external relations, and
financial condition, which must be able to prevent business interruption and support the
value of indemnifications.
__ .
P7JL5 Initial Assessment
Sites will be assessed against Solutia as the standard.
The initial assessment is intended to be thorough and to cover
environmental compliance,
groundwater history/protection,
safety and IH status and programs,
' .waste management,
knowledge of Solutia technology, and
.
general knowledge/performance against the tenets of Responsible Care or similar programs
worldwide.
Continued on next page
DSW 122293
P7-5 COMPANY CONFIDENTIAL
WATER PCB-SD0000021273
P7.2 TOLL MANUFACTURERS, Continued
VJJ2.6 Reassessment
and Additional Requirements
Periodic reassessment will be conducted at least every three years.
For those operations under contract to Solutia, tollers must also have a
* spill response plan, and Groundwater Protection Plan.
P7.2.7 Waste Management
Toll manufacturers, including bulk terminals and transloading, will
* take title to, adopt and own any wastes generated, and manage than as their own under manifests and contracts.
V1JU& Shipping Operations
Toll manufacturers involved in shipping of hazardous or regulated materials for Solutia will be supported and controls verified to be in place at the same level as such operations at Solutia locations.
VI.13
Where feasible and desired by the Director of Manufacturing, costs of toller assessment,
Cost Accounting oversight and management will be borne by the tolled products at the cost-of-goods level.
P7.2.10 Waivers
The Director ofManufacturingiis^uthorized to
' \ I ^J \1 il A, \\
reduceihe scope of assessments whereVhrrante&_J war. v<ejrequ.i;rement/s/ioci pr1i--or\asses/sm--ents\oricointracts
.imiallnon. naliitttations,.
and
accept, conditionally orotherwisCTajiy deficiencies notedin theassessments.
Any such waivers must be resolved or reapproved every three years or less^Where
improvements are stipulated as a condition of approval, the work plan will be reviewed
annually.
__
VJJ2.11 Exclusions
Vendor equipment tests or bench-scale manufacture ofsmall quantities/samples are conditionally excluded, dependent on
coverage by purchase order or contract, Solutia stipulation of return of materials or disposal method/location of wastes, and exchange of material safety and handling information.
P7.2.12 Termination
A termination plan, put into place when toll operations are initiated, will be executed when
operations are discontinued.
-
filcname:sol7.doc fin Neman M-publicl rev. 6/9/98
DSw 122294
P7-6 COMPANY CONFIDENTIAL
WATER PCB-SD0000021274
Program GEN4 Community Awareness at Manufacturing Sites
OVERVIEW
Introduction Policy
Goals Measuring Progress
i This program describes the policies, goals, standards and procedures necessary to implement Solutia's commitment to "keep our operations open to our communities, andfoster open '
communications with all ofour stakeholders.'
The company will
foster its employees' and the public's right-to-know through openness, involvement and and
be responsive to questions and concerns about human safety, health and the environment at
its manufacturing sites.
~
The company will openly share information on safety and the environment and establish and maintain community advisory panels at manufacturing sites.
The following ii idicatcirsw ill-beused to irieasure progress against tEjte'gpal:
i') /^,\ i r- . | I ^
* Active' communiry-ddvisory panels at manufacturing siteS_i
Participation in training and planning for Risk Management Program communications.
Annual dissemination of data on toxic chemicals and other chemicals of local concern.
Wide distribution of the Environmental Annual Review to report the company's status against stated environmental, safety and health goals.
Progress toward developing routine and convenient ways (such as internet access) for
interested parties to become familiar with the company's
.
> manufacturing sites, operations, - products, and - efforts to protect human safety and health and the environment.
Continued on next page
DSM 12ZZ9S P8-1 COMPANY CONFIDENTIAL
WATER PCB-SD0000021275
OVERVIEW, Continued
For Further Information
When further information or clarification is required, you may contact the following:
ISSUE OWNER
John L. Henshaw, ESH Region 3, F2EP
(314)674-8830
....
TECHNICAL CONTACTS Kevin S. Cahill, Public/Govemment Affairs, G4WA (314)674-7518
Beth L. Rusert, Public/Govemment Affairs, G4WA (314)674-8527
Loren W. Wassell, Public/Govemment Affairs, G4WA (314)674-7002
Program Approval
The content of this program was approved by
In This Program This program contains the following procedures. ...-C 1 ^ ] | Procedure' \ j 1-------- | |
ps. i ""edMMUNror involvementand dialogue P8.2 INFORMATION ON CHEMICAL RELEASES/INCIDENTS
See Page P8-3 P8-5
DSW 1222-96
P8-2 COMPANY CONFIDENTIAL
WATER PCB-SD0000021276
P8.1 COMMUNITY INVOLVEMENT AND DIALOGUE
P8.1.1 Introdaction
This section describes procedures to be used to accomplish the company's specific goals for
community involvement and dialogue.
.
P8.1J
Each manufacturing site will implement a policy of openness that provides convenient ways for
Openness Policy interested individuals to become familiar with the facility and its
operations, products, and efforts to protect human safety, health and the environment.
.
P8.1J Activities
To involve the community plant operations, the following activities, among others, may be
used:
\
community advisory panels, open houses, /\ plant tours, am \ environmental awareness days.
P8.1.4 Community Outreach
Community outreach programs will be implemented at each manufacturing site to inform key
audiences (emergency responders, government officials, the media, employees, other businesses
and the community) about the facility's
.
emergency rIesponsenpro! gram, -j // a \\
chenucaHnyentor^, j => /A\
impacrevalnatian,' ^hd
i ] r.-->.
potendalrisksTOTfie community.--
P8.1.5 Information Details
The information provided will include details on such topics as
waste minimization, emissions reduction, health effects of chemicals, and efforts to ensure safe transport of chemicals.
--'
All information will also include planned improvements in each of these critical areas as well as expansion activity and other projects of general interest to the community.
P8.1.6 Ongoing Communications
An ongoing dialogue with employees and members of the community will be used to
assess and respond to their questions and concerns about environmental, safety and health issues, and
involve them in the community outreach effort.
Continued on next page
J)SW 122*97
P8-3 COMPANY CONFIDENTIAL
WATER PCB-SD0000021277
P8.1 COMMUNITY INVOLVEMENT AND DIALOGUE, Continued
P8.1.7 Assessments
Each manufacturing site will conduct an ongoing assessment of employee and community questions and concents about the site. The effectiveness of the ongoing community communications effort will be evaluated regularly by the site.
P8.1.8 Training
Communications training will be provided for key site and company personnel who communicate with employees and the public concerning human safety, health and the environment
122298
P8-4 COMPANY CONFIDENTIAL
WATER PCB-SD0000021278
P8.2 INFORMATION ON CHEMICAL RELEASES/INCIDENTS
PS %i Introduction
This section describes procedures to be used to accomplish the company's specific goals regarding information on chemical releases and safety.
py ) t
Releases/ Safety Information
Each operating location will make available to appropriate audiences (neighbors in the community, employees and/or the news media), timely information about
* routine or accidental releases of toxic and other chemicals of local concern, and
progress and future plans for achieving the company's stated goals to reduce emissions, prevent pollution and improve safety.
PS lt Personal Communications
When possible, the information on chemical releases/safety should be at a personal, face-toface level and should emphasize listening to others and discussing their concerns and ideas.
1
P8.2.4 Annual Publication
The company will publish and distribute an Environmental Annual Review that articulates the
company's
'
environmental, safety and health policies, and
progress toward achieving stated environmental, safety and health goals.
nienamersois.ac ciiruiNenn n-MDuonc) rev. o/y,
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y
,ii_-____--__
^
OSW . L22293
P8-5 COMPANY CONFIDENTIAL
WATER_PCB-SD0000021279
Program GEN5 Environmental, Safety and Health Reviews of Capital Projects
OVERVIEW
P9 j Introduction
This program describes the policy and procedure to be used for environmental, safety and health reviews of capital projects.
P9.2 Policy
The company's capital projects will
meet Soluda policies, goals, standards and procedures,
be in compliance with existing and anticipated governmental regulatory requirements, and
be reviewed at all levels for environmental, safety and health impact before, and as a condition of, project funding.
P9J Responsibilities
The Vice President, Environmental, Safety and Health or his/her designee will review those projects requiring approval by the Chief Operating Officer (COO), the Chief Executive Officer (CEO) or the Boardof.Directors. (gOD).Jhc ESHRegional Leads will participate in the project Majors ccoontobiUty'ftThemise (MAP) reviews'!.1
A systemjr*.re' iewing o'dler smallerprojects Will be established afjluCsites with ESH Shared
Service. "" 1-------- ' u ^ ^ ^ ^
LJ
P9.4 Procedure
.
P9.5 Exceptions Approval
P9.6 For Further Information
The Company will follow the CPM and New Fixed Investment Management Process. The effects of the public climate of opinion and of existing and future governmental, "" " environmental regulations that may apply also are to be considered. Employees assigned to evaluate a new location for operation will prepare an internal environmental impact assessment addressing potential environmental limitations at the site as a result of the existing socioeconomic and biophysical conditions.
Any exceptions to this document must be approved by the Solutia Leadership Team.
When further information or clarification is required, you may contact the following:
ISSUE OWNER John L. Henshaw, ESH Region 3, F2EP (314)674-8830
` Continued on next page
SW *2*300
P9-1 COMPANY CONFIDENTIAL
WATER PCB-SD0000021280
OVERVIEW, Continued
P9.7
Program Approval
The content of this program was approved by filename:Pldger7.doc (in Nepran M-private) rev. 6/9/98
J
DSM 122301
P9-2 COMPANY CONFIDENTIAL
WATER_PCB-SD0000021281
DSN 122302
WATER PCB-SD0000021282
Program ENV1 Pollution Prevention
OVERVIEW
Introduction Policy
l This program describes the policies, goals, standards and procedures necessary to implement Soluda's commitment to the continuous improvement of our health, safety, and environmental
program.
The company is committed to continuously improve the health, safety, and environmental performance of our products and operations.
We wilt
ensure that our operations and distribution systems are safe for employees, site contractors,
communities and the environment;
'
make products that are safe when used responsibly;
keep our operations open to our communities, and foster open communications with all of
our stakeholders;
/\
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ir i
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continuously improve ourraw'maternPand energy-utilization efficiencies to reduce our
impactoji:the environment and improve the sustainability of ourbusinesses;
encourage active participation in and positive contributions to safety, health, and
environmental stewardship by our employees; and*
~
search worldwide for new technologies that bring environmental, safety and health va2ueJsr all of our stakeholders.
Continued on next page
DSW 122303
Pi-1 COMPANY CONFIDENTIAL
WATER PCB-SD0000021283
OVERVIEW, Continued
Goals
These specific goals must be integrated into raw material yield and energy improvement plans for each business.
Compliance Date
Goal
End of 1998 l
Define major products supported by deep well injection and major energy consuming products for enterprise focus.
P-a<* business will establish baselines for raw material yields, energy utilization and associated five year improvement targets. Businesses will also establish tracking mechanisms to measure continuous improvement consistent with corporate direction issued to ensure consistency.
Measuring Progress
The following indicators will be used to measure progress against these goals:
* Achievement of contingency planning for withdrawal from injection wells, if required.
Annual verification of no new uses of deep well injection.
Reduction df total organicjejeases and"SARA reportahle inorganic releases to deep
u >;jinjectionVvells perpbundLofLproduct manufactured^ Data will be-tcacked for defined major
products making usc/of injection wells^ x
1_: Li U \_A
r-
Reduction in total BTUs required to manufacture defined major energy consuming
products.
Continued on nexi page
DSU 122304
Pl-2 COMPANY CONFIDENTIAL
WATER PCB-SD0000021284
OVERVIEW, Continued
For Farther Information
When further information or clarification is required, you may contact the following:
GENERAL POLICY MATTERS Garth F. Fort (314)674-8886
SECTOR LEAD - WASTE PROGRAMS J. Pat Hyland (314)674-6715
SECTOR LEAD-AIR PROGRAMS David S. Krawczylc (314) 674-3666
.
SECTOR LEAD - WATER PROGRAMS Steven D. Smith (314)674-4660
Program .Approval
The content of this program approved by
In This Program
Procedures
Pl.l Reducing Releases and Emissions from Process and Nonprocess Waste
P1.2 Underground (Deep Well) Injection Waste P13 Handling Land Disposal and Land Application P1.4 Assessing Impact of Air Emissions Pl-5 Assessing Impact of Water Releases
See Page
Pl-4 Pl-5 ~~ PI-6 Pl-8 PI-9
'SW 122305
Pi-3 COMPANY CONFIDENTIAL
WATER PCB-SD0000021285
P1.1 REDUCING RELEASES AND EMISSIONS FROM PROCESS AND NONPROCESS WASTE
PI.1.1 Introduction
This topic describes procedures to be used to accomplish the company's specific goals for improving raw material yields and reducing energy requirements to ensure no negative impact to people and the environment from our products and operations.
pi.1.2 Integration of Corporate Goal into Business Plans
The businesses will integrate this corporate goal into their business plans and will utilize key measures established to ensure consistency of approach to track progress.
.
P1.1J Additional Improvement Measures
Continuing measures to improve raw material yields and reduce energy requirements include:
.
the emphasis of the development and use of new manufacturing and energy conservation
projects and technologies, and
aggressive evaluation and implementation of co-product and product recyclefreuse
opportunities
customer and product user interface to identify recycle/reuse and product modification
opportunities
PI.1.4 Nonprocess Waste Yield and Energy Tracking
The above data will be compiled annually beginning with calendar year 1995. Key raw materials will be selected by the businesses for quarterly tracking using the balanced scorecard approach.
Sw 122306
Pi-4 COMPANY CONFIDENTIAL
WATER PCB-SD0000021286
P1.2 UNDERGROUND (DEEP WELL) INJECTION WASTE
P1JL1 Introduction
This topic describes procedures to be used to accomplish the company's specific goals for deep well injection wastes.
Pl^-2
Contingency Plan for Deep WeU Withdrawal
The company will use the following methods to prepare for the potential of regulations mandating the withdrawal from deep wells.
Perform study-grade estimates to achieve non-brine, treated surface discharge to select optimal technical strategies for total withdrawal from deep wells, and
Continue to challenge the technical impediments to total withdrawal from deep wells.
P1JL3 New Uses of Deep Wells
New internal or external uses of deep wells are not permitted unless prior approval of the Policy/Planning Team is obtained.
A new use ofdeep wells is defined as
injection of streams from new products,
.
the addition of substances not previously injected, at that site
injection of remediation wastes not previously disposed of by deep well injection
SW
Pi-s COMPANY CONFIDENTIAL
WATER_PCB-SD0000021287
P1.3 HANDLING LAND DISPOSAL AND LAND APPLICATION
PU.1 _ Introduction
This topic describes the procedures to be used to accomplish the company's specific goals for
handling land disposal and land application.
.
PUJ
I .andfill
The company will not practice landfill of
acutely hazardous wastes, and incinerables.
NOTES:
Acutely hazardous wastes are those listed in 40CFR261.33(e), plus any mixtures containing
greater than 5 percent of the listed wastes.
-
Incinerables are hazardous wastes or wastes managed as hazardous, with a heat of combustion greater than 6000 BTU/lb.
P1JJ Hazardous Waste and Managing Wastes as
Hazardous
For hazardous wastes and wastes managed as hazardous, fixation of particularly mobile, persistent or bioaccumulative wastes will be accomplished whenever warranted and feasible. When making the decision to manage wastes as hazardous, the company will take into account
public expectations, emerging trends, and worldwide company practice regarding the same or similar wastes.
'
P1J.4
The compiainy. will^ubj^ct contractors4ired-fok land disposal of proc^wastes to contracting
Off>Site Landfills and assessment requirements, as described iriPirogram 7, Outside Processors.
In the United States, the use of off-site hazardous waste landfills will be
approved by the Policy/Planning Team and limited in number.
PIJi Medical Wastes
Company sites will arrange to
* incinerate medical wastes generated at the company's locations, prior to land disposal of residues, and
obtain assurance of incineration of medical wastes via manifests or equivalent documents.
Pl.3.6 Non-Soluda Wastes
The company will discourage use of Soluda facilides to commercially treat, store or dispose of non-Soluda wastes. Any such use orjoint ventures (other than in-site guest/host relationships) . must be reviewed and approved by the Policy/Planning Team.
Continued on next page
OSW 122308
Pi-6 COMPANY CONFIDENTIAL
WATER_PCB-SD0000021288
P1.3 HANDLING LAND DISPOSAL AND LAND APPLICATION, Continued
P1J.7 Land Application of Process Byproducts and Residues
The company will prepare proposals for land application of process byproducts and residues, for beneficial use or disposal, by using as guidance the Monsanto Guidance Document: Land Application ofProcess Byproducts and Residues.
The ESHA discipline (including 5-year reviews) will be followed.
Pljj Land Application Approval
The company will require approval of all new applications by the appropriate [Business General Manager and the ESH Policy Director.]????
The Policy/Planning Team must approve new applications if beneficial use is not included.
P1JJ) Documentation
F-arh company location will maintain a record of the on-site and commercial waste treatment. storage and disposal sites it uses.
/\
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][
-DSW 122309
Pi-7 COMPANY CONFIDENTIAL
WATER PCB-SD0000021289
P1.4 ASSESSING IMPACT OF AIR EMISSIONS
Pl.4.1 Introduction
.The company will assess air emissions from new processes or new businesses or existing businesses as new information on potential hazards might dictate.
DSW 122310
Pl-8 COMPANY CONFIDENTIAL
WATER PCB-SD0000021290
PI.5 ASSESSING IMPACT OF WATER RELEASES
pu.1 Introduction
The company will assess releases of water pollutants from new processes or new businesses or existing businesses as new information on potential hazards might dictate.
I nlename:sol lmwm.doc (in Nepran M-public) rev. 619198
OSH L223LI
Pi-9 COMPANY CONFIDENTIAL
WATER PCB-SD0000021291
OVERVIEW
Program ENV2 Groundwater and Soil Quality
Tntrodurtfr"
Policy
.
This program describes policies, goals, standards and procedures necessary to implement the groundwater and soil quality aspects of Soluda's commitment to "... ensure that our operations. .. are safe for... the environment"
The company will
design and operate facilities to protect groundwater and soil quality,
groundwater and soil quality at its facilities,
pursue remedies for releases that threaten health or the environment, and
address on-site and off-site containment of groundwater and soil attributable to its operating and waste practices to ensure protection of health and the environment
Ensure there are no adverse public health impacts attributable to the company's wastes.
Minimize the financial impact of remedial action and third-party liability attendant to wastj, sites.
* Resolve, as soon as reasonably possible, the company's share of liability and remedial plans for Superfund sites where it has a responsibility, while securing timely and cost-effective resolution.
Measuring Progress
To measure progress against these goals, there will be an annual groundwater assessment at - - - each site..
For Further Information
When further information or clarification is required, you may contact the following:
ISSUE OWNER Bruce S. Yare, ESH Remediation, F2EA (314)674-6370
Program Approval
The content of this program was approved by .
. Continued on next page
P6-1 COMPANY CONFIDENTIAL DSU 122312
WATER PCB-SD0000021292
OVERVIEW, Continued
In This Program This program contains the following procedures.
.
P6.1 ASSESSMENT P6.2 PROTECTION P63 SUPERFUND
Procedures
SeePage
P6-3 P6-4. P6-5
122313
P6-2 COMPANY CONFIDENTIAL
WATER_PCB-SD0000021293
P6.1 ASSESSMENT
P6.1.1 Introduction
This section describes assessment and response procedures used to accomplish the company's
specific goals to
.
establish an active groundwater assessment program in its facilities, and
ensure there are no adverse public health impacts attributable to the company's wastes.
P6.1.2 Assessment Plans
Programs for assessment and tracking of groundwater quality will be organized at
all major locations, and lesser sites that have known groundwater issues.
P6.1-3 Corrective Action
Appropriate assessment of impacts on human health and the environment will be carried out when on-site waste or groundwater and/or soil contamination is discovered.
Corrective action will be taken, as necessary, in a planned, orderly process to remediate soil or groundwater impacts that threaten human health and the environment
P6.1.4
Newly Purchased
Sites
Any newly purchased, existing operation will be subjected to the seven-point protocol for
assessment of possible groundwater contamination. The issue owner of this chapter will supply
a copy of the assessment protocol upon request.
rzr'-N i
/ \ iji
P6-3
SW 12*31*
COMPANY CONFIDENTIAL
WATER_PCB-SD0000021294
P6.2 PROTECTION
P&2.1 Introduction
This section describes operating and design procedures used to accomplish the company's specific goals to ensure there are no adverse public health impacts attributable to the company's wastes.
P63-2
Groundwater Protection Plans
Each location will maintain a Groundwater Protection Plan that includes inspection, testing and maintenance of facilities that could contaminate groundwater, e.g.
I
sewers, process lines, sumps, tanks, and loading/unloading areas.
_
The groundwater protection plans and designs will be commensurable with the risk posed by
the specific situations.
.
P6.2_3 Facility Design
To provide improved assurance against groundwater contamination, new, replacement or expansion facility designs (including sewers and lines) will consider such options'as
aboveground and/or double containment,
improved materials of construction, and/or
cathodic protection.
| :____f~\ i
ii
New, replacement or expanded surface impoundments for wastewatet.treatment or storage must
be approved by the Policy/Planning Team-on an exception basis. '>'j
P6.2.4 Storage Tanks
New storage tanks for materials that could cause contamination will be provided with impervious secondary containment (e.g. dikes, liners, vaults, double wall) unless a clear showing is made on a tank-by-tank basis during project reviews that vessel contents (e.g. dilute wastewaters) or setting (e.g. in-battery containment or other adequate containment systems) do, not warrant such containment.
Existing storage tanks will be reviewed in normal environmental audits.
DSW L223L5
P6-4 COMPANY CONFIDENTIAL
WATER_PCB-SD0000021295
P6.3 SUPERFUND
P63.1 Introduction
`
This topic describes procedures used to accomplish the company's specific goals to
minimise the financial impact of remedial action and third-party liability attendant to waste
sites, and
...
* resolve its share of liability and remedial plans for sites where it has a responsibility while securing timely and cost-effective resolution.*
P6J.2 Action to be Taken
' When the company becomes aware of involvement in "Superfund" sites, it will act to ensure that there are no public health impacts attributable to its wastes, actively participate in potentially responsible parties' efforts to achieve settlement, and
e, when appropriate, to facilitate resolution.
The business units will cooperate to establish responsibility for sites where several units contributed wastes.
P6J_3
The company intends a lessened legalistic approach to site cleanup negotiations through the
Legal Approach following actions:
.
filename.sol6.doc (in Nepran M-public) rev. 6/9/98
DSW 122316
P6-5 COMPANY CONFIDENTIAL
WATER PCB-SD0000021296
OVERVIEW
Program ENV3 Ozone Depleting Chemicals
p!6.1 Introduction
This program describes the policy, scope and site applicability for minimizing the uses and environmental releases of ozone-depleting chemicals (CFCs).
P16J. Policy
The company will
initiate actions at all of its sites worldwide to minimize the uses and environmental releases of the chemicals subject to this program, and
seek out acceptable substitute chemicals, when possible.,on or before applicable compliance date* set by the site's local country laws and regulations.
PI 6.3 Scope
The following chemicals are those listed in the Montreal Protocol and are the minimum number subject to this policy.
CFC-11 CFC-12 CFC-113~H^\ CFC-Tlk i )
^EC-115 - J j
Halort lizCd-' Hal on-1301
Halon-2402 CFC-13 CFC-111
CPC-112
CFC-211
___ s '-CF0212 :--' >CFC-2li
-------------- i|--
!___
.-- \, 'CFCSM J1 ': 1 JCTC-21S-J
CFC-216
CFC-217
Carbon Tetrachloride
Methyl Chloroform
Each company site should add to the list any other chemicals of local country concern and treat them according to this policy in conformance with local country laws and regulations.
P16.4
Company sites subject to this policy include the following sites where the company owns or
Applicable Sites operates facilities that use or contain one of the chemicals subject to this policy:
. plants, offices,
. R&D facilities, sales offices, and
. warehouses.
This coverage includes any subsidiary in which the company is a greater than 30 percent owner.
Continued on next page
P16-1
-0SW 12231?
COMPANY CONFIDENTIAL
WATER PCB-SD0000021297
Ozone Depleting Chemicals, Continued
P1&5 For Farther Information
When further information or clarification is required, you may contact the following:
ISSUE OWNER TPfHNICAL CONTACT: Deborah K. Grissett, Senior Environmental Engineer, 1690 (850)968-8839
P16.6 Program Approval
The content of this program was approved by fi1enamc:sol 16.doc fin Neoran M-oublic) rev, 6/9/98
Pi 6-2
DSW 122318
COMPANY CONFIDENTIAL
WATER PCB-SD0000021298
IV . SAFETY
OSH L223L9
' WATER PCB-SD0000021299
draft
SOLUTIA INC. SAFETY MANAGEMENT PROCESS
1.0 INTRODUCTION
1.1 Solutia Commitment Statement
1.2 Purpose
13 Scope
1.4 - For Further
Information
It is our commitment to ensure our operations and distribution systems are safefor employees, guests, communities and the environment.
These safety requirements support Solutia's ESH Commitments and additional efforts in Solutia's Voluntary Protection Program, Responsible Care, and the Behavior Based Safety Process by defining the safety systems necessary to control risks in Solutia's manufacturing facilities. This document describes, in broad terms, the required elements of these systems and defines the level of hazard that a process/operation offers.
This document applies to worldwide manufacturing operations where Solutia has direct operation control. Application of its concepts is encouraged in all other Solutia relationships.
''
When further information or clarification is required, you may contact the following:
John V. Birtwistle Paul M. Villane Dale E. Dressel
lJ Document Approval
This document was approved bv the Solutia on .
Safety Proc.doc
Page-1
OSH 122320 Rev. 1/15/98
WATER PCB-SD0000021300
DRAFT 1.0 INTRODUCTION, Continued
1.6 la This Document
This document contains the following sections:
.
Section 1.0 Introduction 2.0 General Requirements 3.0 Tiered Requirements/Hazard Levels 4.0 Variance Procedure 3.0 'Safety Guidance Documents
See Page
1 3 4 7 8
| .
Safety Proc.doc
Page-2
J)SW 122321 Rev. 1/15/98
WATER PCB-SD0000021301
draft
2.0 GENERAL REQUIREMENTS
2.1 General ..
Requirements
These are the minimum requirements for all Solutia sites. Where state, federal, or country regulations are more stringent, they take precedence. Programs with tiered requirement levels (Items 2.12 through 2.15) are discussed in Section 3.0 and the individual requirements document.
2.2
Safety Requirements
Document Number Requirement 2.1 Safety Program Management
22 2.3 2.3.1 2.4 2.4.1 2.4.2 2.4.3 2.4.4 2.4.5 2.5 2.6 2.7 2.8 2.9 2.10 2.10.1 2.102 2.10.3 2,11 2.12 .2.13 2.14 2.15 2.16
.
Contractor Guest Safety Incident Investigation
'
Incident Loss Report
Safe Work Practices and Operating Procedures
Lockout/Tagout Program
Hot Work Permit
Confined Space Entry
Breaking Into Pipelines & Equipment
Temporary Connections/Installations/Situations
Security
Emergency Response
Interlock Management
.
Volunteer Protection Program (VPP) Participation
High Hazard Material (HHM) Management Program
Fire Protection
Fire Protection Impairment Control
Fire Protection Equipment Inspections
Acceptance ofNew Fire Protection Installations
ESH Compliance Audits
Training
Mechanical Integrity
Process Hazard Analysis
Management of Change
Solutia Injury/Illness Classifying and Reporting Decision Process
-
Safety Proc.doc
Page - 3
DSW 122322 Rev. 1/15/98
WATER PCB-SD0000021302
draft
3.0 TIERED REQUIREMENTS/HAZARD LEVELS
3.1 Introduction
This section describes the approach of Tiered Requirements and the Hazard Levels involved in the management of Safety programs. Refer to the individual requirement documents for more details.
3.2
Tiered Requirement Programs
.
Tiered Requirements have varying degrees of effort and complexity depending on
the program and hazard level. In general, the higher the hazard, the more diligent
the control measure.
.
'
Tiered requirement programs include: '
ESH Compliance audits Training Mechanical Integrity Process Hazard Analysis, and Management of Change
* .
3.2.1
Auditing
' The intent of the ESH compliance audits are to:
confirm that regulatory and Solutia requirement requirements are being met, provide objective feedback to both the location and management that systems
are in place and functional, assess safety management and control systems are designed to assure
compliance and conformance, and assess Safety conformance with industry accepted standards and good practice.
3.2.1.1 ESH
Compliance Audit
Techniques
The techniques for ESH Compliance Audits are as follows:
Level 1 2 3
Audit Group Safety Regional (Corporate) Safety Plant Process Unit
Safety Proc.doc
Page-4
DSW L22323 Rev. 1/15/98
WATE RPC B S D0000021303
DRAFT
3.0 TIERED REQUIREMENTS/HAZARD LEVELS, Continued
3JL2
Training
The intent of training is to:
inform the employee (functional, awareness, and management levels) of recognized hazards in the workplace,
provide skills so the work can be conducted in a safe and healthy manner for himself, co-workers and the community, and
determine the understanding ofthe material for which the training was conducted.
3.2.2.1 Training
The requirements for training are summarized in the requirement procedure.
3-2-3 Mechanical The intent of mechanical integrity is to have a documented mechanical integrity
Integrity
system which includes the following elements:
. * appropriate design standards,
vessel and piping inspection system,
reliefdevice testing system,
. * tire protection inspection system, and
`
system to control replacement of equipment and parts.
These requirements will be tiered as described in applicable corporate and site ESH Procedures and engineering standards.
3.2.4 Process Hazard Analysis (PHA) Requirements
The intent ofprocess hazard analyses is to:
_
identify, evaluate and control the hazards in the process, assign a priority to the recommendations developed, and provide documentation of the review.
3.2.5 Management of Change .
The intent of management of change is to:
provide a technical basis for the proposed change, assess the impact ofthe change on safety & health, identify required modifications to written documents, identify time period required to incorporate the change, and provide authorization for the change.
Safety Proc.doc
Page - 5
D.SW 122324 Rev. 1/13/98
WATER PCB-SD0000021304
draft
3.0 TIERED REQUIREMENTS/HAZARD LEVELS, Continued
3.3 Hazard Levels
The management of Safety programs is a complex task. In today's environment. elements of Safety are regulated on a number of different levels by national or local laws as well as by internal company requirements and procedures. These requirements
i
provide a holistic view of the Safety programs which provides assurance of external and internal compliance,
provide thorough coverage of all aspects of the Safety programs referred to in this requirement document, and .
optimizes resources needs with the establishment of clear requirements.
are based upon defining the level ofhazard that a process/operation can offer to the employees that work there. .
The following table defines these hazards levels
3.3.1 Hazard Levels
Table
The following table defines these hazard levels:
Level 1
Is a hazard that... can create an immediate life threatening event at the facility fenceline.
-2 3
can create an immediate life threatening event inside the facility or cause health impacts or evacuation outside the facility fenceline. can cause health impacts, personal injury or environmental impact inside a facility.
4 is not beyond those managed by general manufacturing safety practices.
This includes... release of toxic-chenficals,
and vapor cloud explosions release of toxic chemicals,
and . vapor cloud explosions
chemical fires, toxic releases, and vapor cloud explosions transportation, personnel safety, and fire protection
j
Safety Proc.doc
Page - 6
-DSW 122325 Rev. 1/15/98
WATER PCB-SD0000021305
DRAFT 4.0 VARIANCE PROCEDURE
4.1' Purpose
The purpose of a formal variance procedure is to allow deviations from the requirements in this document. It should be recognized that while these requirements are generally applicable to all facilities, circumstances may dictate the best course of action is a formal variance request, reviewed and approved by management.
4.2 Variance Requested Elements
The variance request shall include the following elements:
a statement requesting a variance
a statement of the deviation and its duration, as existing or proposed, referencing the Safety requirement involved.
an assessment ofthe hazards and consequences associated with the deviation, and .
an explanation of the proposed variance request would deal with the above.
Step 1 2 3 4
5
Action
The variance request is submitted to the location's Director of Manufacturing (or equivalent). Director of manufacturer (or equivalent) determines who should review the document. Document is reviewed and comments are gathered. Appropriate disposition of the variance requested is determined* location is notified of results and action plans. All active, approved variances are reviewed during the site's ESH auditing process.
Safety Proc.doc
Page - ^
OSH 1Z2326 Rev. 1/15/98
WATER PCB-SD0000021306
health
DSW LZ232*?
WATER_PCB-SD0000021307
SOLUTIA INC. INDUSTRIAL HYGIENE MANAGEMENT PROCESS
1.0 INTRODUCTION
1.1 Solutia Commitment Statement
1.2 Purpose
1.3 Scope
1.4 For Further Information
It is our commitment to ensure our operations and distribution systems are safefor employees, guests, communities and the environment.
Industrial Hygiene Requirements support Solutia's efforts in Solutia's Voluntary Protection Program, Responsible Care, and the Behavior Based Safety Process by defining the industrial hygiene systems necessary to control health risks at Solutia's locations. This document describes, in broad terms, the required elements ofthese systems.
This document applies to worldwide manufacturing operations where Solutia has direct operation control. Application of its concepts is encouraged in all other Solutia relationships.
When further information or clarificationis required, you may contact the following;
Paul E. Shelton Steven N. Hacker Janet L. Weaver
'*"*
--
1.5 Document Approval
This document was anproved bv the Solutia
- on
.
IH ManPro.doc
Page-1
DSW 122328 Revised: 01/15/98
WATER PCB-SD0000021308
1.0 INTRODUCTIONjContinued
)
1.6 la This Document
* ' This document contains the following sections:
*
Section 1.0 Introduction.. 2.0 General Requirements 3.0 Tiered Requirements/Hazard Levels 4.0 Variance Procedure 3.0 IH Guidance Documents
See Page |
1. 3 .
4 7 8
IH ManPro.doc
Page-2
DSW 122329 Revised: 01/15/98
WATER_PCB-SD0000021309
2.0 GENERAL REQUIREMENTS
2.1 General Requirements
These are the minimum requirements for all Solutia sites and where state, federal, or country regulations are more stringent they take precedence.
2.2 IH Requirement Documents
Document Number 2.1 22 ' 23 2.4 23
2.6 2.7 2.8 2.9 . 2.10 2.11 2.12
Requirement
Hazard Communication
-
Respiratory Protection Hearing Conservation
Ergonomics
.
Occupational Exposure Control to Ionizing Radiation
Local Exhaust Ventilation
Exposure Assessment/Monitoring Frequency
Chemical Control
Monitoring Data Integrity
Automatic Continuous Area Monitors
Chemical Protective Clothing/Gloves
Laser Safety Program
IH ManPro.doc
Page -3
DSW 122330 Revised: 01/15/98
WATER PCB-SD0000021310
3.0 TIERED REQUIREMENTS/HAZARD LEVELS
3.1 Introduction
This section describes the approach ofTiered Requirements and the Hazard Levels involved in the management of Industrial Hygiene programs.
32 Tiered Requirement Programs
Tiered Requirements have varying degrees of effort and complexity depending on the program and hazard level. In general, the higher the hazard, the more diligent the control measure.
Tiered requirement programs include:
Compliance audits Training Routine maintenance/Calibration Monitoring/Assessments
..
3.2.1 Auditing
The intent ofthe audits are to: '
confirm that regulatory and Solutia requirements are being met,
provide objective feedback to both the location and management that systems
are in place and functional,
.
assess IH management and control systems designed to assure compliance and
conformance, and
assess IH conformance with industry accepted standards and good practice.
32.1.1 Audit Techniques
Level 1 2 3
Audit Group IH Regional (Corporate) IH Plant Process Unit
`
IH ManPro.doc
Page -4 r.
DSW LZ233J. Revised: 01/15/98
WATER PCB-SD0000021311
3.0 TIERED REQUIREMENTS/HAZARD LEVELS. Continued
3.2.2 Training
The intent of training is to:
inform the employee (functional, awareness, and management levels) of
recognized hazards in the workplace,
' provide skills so the work can be conducted in a safe and healthy manner for
himself, co-workers and the community, and
..
determine the understanding of the material for which the training was
conducted.
3.2.3 Maintenance/ Calibration
The intern of maintenance/calibration is to:
evaluate systems designed to minimiye employee exposure to hazardous
materials to determine ifthey are operating at design specifications and
ensure that results are a valid determination of the exposure monitoring and to
compare to regulations and guidelines.
'
3.2.4 Monitoring/ Assessments
The intent of monitoring/assessment is to:
document qualitative and quantitative exposure potential determinations for comparison to recognized exposure limits and guidelines, as well as good industry practices.
EH ManPro.doc
Page-5
DW 122332 Revised: 01/15/98
WATER PCB-SD0000021312
3.0 TIERED REQUIREMENTS/HAZARD LEVELS, Continued
33
Hazard Levels
The management ofIndustrial Hygiene programs is a complex task. In today's environment, elements ofIndustrial Hygiene are regulated on a number of different levels by national or local laws as well as by internal company requirements and procedures. These requirements: i
provide a holistic view of the Industrial Hygiene programs which provides assurance of external and internal compliance,
provide thorough coverage of all aspects of the Industrial Hygiene programs
referred to in this requirement document,
--
optimizes resources needs with the establishment of clear requirements, and
are based upon defining the level of hazard that a process/operation can offer to the employees that work there.
The following table defines these hazards levels.
Level 1
2 3
is a hazard that...
can create an immediate life threatening event at the facility fenceline or inside the manufacturing department (e.g., ERPG 3 (Emergency Response Planning Guidelines)), relates to the handling of regulated chemicals and known or suspected human carcinogens in manufacturing processes. is related to any material with a recognized exposure limit, has a IDLH value not previously addressed by ERPG 3 values, is a significant physical hazard.
is considered a hazardous chemical, but has no recognized exposure limit.
This includes...
|
OSHA regulated chemicals. materials with ERPG-3 values, any material with a country specific regulation,
human carcinogens
PEL'S, TLVs, MAK's, etc..
Ergonomics
noise
radiation
dusts NOC,
.
p-nitrophenol,
boric acid,
some consumer products
IH ManPro.doc
Page - 6
DSW 122333 Revised: 01/13/98
WATER PCB-SD0000021313
4.0 VARIANCE PROCEDURE
4.1 Purpose
The purpose of a formal variance procedure is to allow deviations from the requirements in this document. It should be recognized that while these requirements are generally applicable to all facilities, circumstances may dictate the best course of action is a formal variance request, reviewed and approved by management.
4.2 Variance Requested Elements '
The variance request shall include the following elements:
a statement requesting a variance
`'
a statement ofthe deviation and its duration, as existing or proposed, referencing the IH requirement involved.
an assessment of the hazards and consequences associated with the deviation, and
an explanation of the proposed variance request would deal with the above.
43 Procedure
Step 1 2 3 4
5
Action
--
The variance request is submitted to the location's
Director of Manufacturing (or equivalent).
Director of manufacturer (or equivalent) determines who
should review the document
.
Document is reviewed and comments are gathered.
Appropriate disposition of the variance requested is
determined, location is notified of results and action
plans.
All active, approved variances are reviewed during the
site's EHS auditing process.
IH ManPro.doc
Page - 7
DSW 122334 Revised: 01/15/98
WATER PCB-SD0000021314
5.0 IH GUIDANCE DOCUMENTS
5.1 Documents
Available
The following documents are available for additional guidance for Solutia IH issues. Contact your regional IH professional for copies, ifneeded.
1 5.1.1 5.1.2
IH Bulletins IH Audit Protocol
--
IH ManPro.doc
Page-8
OSH 1.22335 Revised: 01/15/98
WATER PCB-SD0000021315
DSW 122336
WATER PCB-SD0000021316
OVERVIEW
Program PS1 Product Stewardship
Introduction Policy
Goals
This program describes the policies, goals, standards and procedures necessary to fulfill the product responsibilities implicit in the Solutia Commitments.
The company will research, develop, design, assess, manufacture, market and dispose of its products so that they
meet ever-increasing societal expectations, and do not pose undue risks to human health or the environment during all stages of their life
cycles.
The company will work with product stakeholders (suppliers, employees, distributors, customers, consumers and disposers) to understand and reduce risks over the life cycle of the company's products.
The following specific goals must be integrated into the company's product stewardship plans.
(MSDSs), to potentially exposed employees, contract employees and product receivers.
NOTE: Materials Safety Data Sheets (MSDSs) and Safety Data Sheets (SDSs) are interchangeable terms and refer to similar requirements in different countries.
* Work toward the goal of no undue risk through systematic risk reduction throughout a product's life cycle.
Incorporate concepts of eco-efficiency into product and process evaluations to improve
their sustainability.
.
Gain a competitive advantage by applying product stewardship principles that add value to the company's product offerings.
Continued on next page
DSW 122337
P4-1 COMPANY CONFIDENTIAL
WATER PCB-SD0000021317
OVERVIEW, Continued
Measuring Progress
To measure progress against these goals, the following indicators will be used:
Demonstrated progress in meeting internal and external requirements for all new product introductions (i.e., NPPD process, ESHA approvals, and governmental approvals);
Demonstrated progress in determining product hazards;
Visible growth in knowledge of the use of company products and the resultant exposures to people and the environment;
Availability of adequate environmental, safety and health data to the ultimate product receiver,
Increased understanding and diminution of the risks and environmental impacts associated with a product throughout its life cycle; and
Differentiation of company products in the marketplace.
For Further * Information
When further information or clarification is required, you may contact the following:
ISSUE OWNER
Jeffrey D. FelderrProdqct Stewardship, F2EC
(314)674-44891
\ I ED ) /a\
Program Approval
The contentof das-pro^ram-was approved by-^ -
In This Program This program contains the following procedures.
- Procedures
P4.1 ESH INFORMATION AND RISK CHARACTERIZATION P4.2 RISK MANAGEMENT SYSTEM P43 PRINCIPLES AND KEY ELEMENTS P4.4 PRODUCT HAZARD EVALUATION
See Page
P4-3 P4-5 P4-6 P4-8
DSW 122338
P4-2 COMPANY CONFIDENTIAL
WATER PCB-SD0000021318
P4.1 ESH INFORMATION AND RISK CHARACTERIZATION
P4.1.1 Introduction
P4.1.2 Definitions
This section describes procedures to be used to accomplish the company's specific goals regarding environmental, safety and health information and risk characterization.
Terms are used in this program as defined in the following table.
Term Product
Product Receiver
Definition
Chemical substances and mixtures, materials and equipment, articles, licensed technology and services related to product use that are sold, distributed in commerce, or otherwise provided.
An entity (not an individual) to whom the company transfers product This includes product receivers such as brokers or transporters who may not fall into the traditional customer category.
P4.1J Product Risk Characterization
A preliminary product risk characterization (ESHA Level 1 to 3, as appropriate, and an R&D
M.beSpDreSp)awreidthfoard.equat^su.pp. ortingen.vironmen, tal.-s, af. ety-tin d-heaHh exposure information will
new-chemical products; . i . / ,------- ^ \\ jj j new isolated process intern)ediatesT and significant new uses for existing chemical products.
>j
An MSDS will be furnished
at the earliest practical stage of R&D, and prior to off-site shipment.
A product risk characterization (including an ESHA Level 4 or equivalent, a final MSDS and a shipping classification) will be completed before new product commercialization.
P4.1.4 MSDS Program
The company's process for generating, reviewing, and maintaining an MSDS is comprehensive and, when coupled with human experience and professional judgment, fulfills the requirement far a product risk characterization for most products. For products with significant inherent hazafd, an ESHA Level 5 is required.
Significant new information will be reviewed in a timely fashion as part of the MSDS program to satisfy regulatory and product risk characterization requirements.
An MSDS review/product risk characterization or an ESHA Level 5 is periodically performed commensurate with product risk. Revisions are performed, at a minimum, every five years, unless waived by the VP, ESH based on a consideration of lack of inherent hazard.
Continued on next page
P4-3 COMPANY CONFIDENTIAL
DSW L22339
WATER PCB-SD0000021319
P4.1 ESH INFORMATION AND RISK CHARACTERIZATION, Continued
P4.1.5 ` Product Files or
Information
Systems
Product files or information systems will be maintained for all products or product families, and
will contain the data necessary to fulfill regulatory requirements and perform product risk
characterizations and assessments as appropriate. The data need not be in a single file or
system but must be readily available to all likely users (e.g. Product Stewardship and other ESH
staff). The'data will include:
.
Relevant information on composition, CAS name and number, common name and synonyms, physical properties, raw materials, manufacturing processes, principal byproducts, protective measures, exposure information, energy requirements, wastes and disposal practices,
References to relevant literature or internal reports dealing with health and safety (toxicology, epidemiology, industrial hygiene, flammability, reactivity, etc.),
Material Safety Data Sheets,
.
Information on product use, including handling, transport, packaging and storage, which will either be
- estimated (typically for new products), or - obtained by visits or reviews of customer, distributor and consumer practices,
A critical review of health and environmental effects and exposure information, such as
DC
ESH Level l\tci 3, asjpjnprjhte\ \
rESHA Level 4i j . ; ! / CL. \ , ,
ESHAlLeicB/ _J Li LJ uL!
> ;i rL
- Solutia Workplace Permissible Exposure Guideline (SWPEG) Reviews,
- Health Effect Reviews, and
- Toxicology Reviews,
Technology Risk Reviews, and
Allegations of health concerns of customers, employees or the public.
O.SW 122340
P4-4 COMPANY CONFIDENTIAL
WATER PCB-SD0000021320
P4.2 RISK MANAGEMENT SYSTEM
P4J.1 Introduction
This section describes procedures to be used to accomplish the company's specific goals regarding systematic risk reduction.
P4.2J, Approach
A systematic approach to risk management will be implemented and maintained for new products. Existing products will be managed on a case-by-case basis.
P4.23 Options
Risk management options, where needed, will be an integral part of the follow-up to each phase of aproduct risk characterization (as detailed in section 4.1, ESHInformation and Risk Characteraation).
P4.Z4
All products will be appropriately labeled for hazard or risk and will conform at a minimum to
Product Labeling pertinent governmental requirements and appropriate consensus standards (e.g. OSHA, EU,
ANSI, ISO, etc.).
P4.25 Documented Actions
Documented risk management actions will be recorded in product files. (Examples of specific risk management actions are detailed in section P4.3, Principles and Key Elements.)
u
osw 122341
P4-5 COMPANY CONFIDENTIAL
WATER PCB-SD0000021321
P4.3 PRINCIPLES AND KEY ELEMENTS
P4J.1 Introduction
This section describes procedures used to accomplish the company's specific goals regarding the principles and key elements of Product Stewardship, including
product and process design and improvement, employee education, product use feedback, information provided to contract manufacturers, distributors, customers and other direct
product receivers, information received from suppliers, and responsibilities involved.
P4.3.2 Productand Process Design and Improvement
R&D materials used in the laboratory will be handled under Prudent Laboratory Practices (as outlined in TSCA Section 5) or equivalent guidance.
Pollution prevention principles (see Program 1, Pollution Prevention) will be included as review criteria in technology risk reviews for new and existing chemicals and will be incorporated into the ESHA, NPPD and equivalent assessments. This includes opportunities for improving energy and resource (e.g. water) efficiency of our products and processes and seeking to replace existing products with those that are more environmentally friendly, as measured by scientifically valid indices that are developed.
P4jJ
Employee Education
P43.4 Product Use Feedback
Employee education in the safe handling and use of chemicals is addressed in Program 2,
Employee and C `SrfSfttmitySafetytmd Health.
j ! 5 --V /a\
<=TrW!------ I
: ! i / !-----V \ j j
M fO""
Employees with significant ~custouiei` uileiacUun will be trained to recognize and feed back to
the company's ESH network, information about product use and misuse.
Feedback systems are appropriate to listen to stakeholders, including commercial and technical
service liaisons with customers, product hotlines, poison control centers, etc.
__ ,
P4J.5 Information Provided to Contract Manufacturers
In addition to items covered in Program 7, Outside Processors, the company will provide
guidance and information to contractor personnel on the safe handling and transportation of
company products.
-
Continued on next page
DSM 122342
P4-6 COMPANY CONFIDENTIAL
WATER PCB-SD0000021322
P4.3 PRINCIPLES AND KEY ELEMENTS, Continued
P4J.6 Information
Provided to Direct Product
Receivers
As appropriate, the company will
ensure that MSDSs and other appropriate safety documents are provided to all direct product receivers,
actively involve product receivers in dialogue and outreach regarding appropriate risk characterization, management and reduction,
i
work with the product receiver, when improper practices involving company products are identified, to improve the practices,
take appropriate action, including termination of sale if necessary, to obtain adequate improvement, and
actively seek product receiver involvement in the continuous improvement of company {noducts and as a means of differentiating those products in the marketplace on the basis of ESH stewardship.
P4J.7 Information Received From . Suppliers
P4.3.8 Responsibilities
Up-to-date product information, sufficient to allow risk management decisions including, as appropriate, composition data and MSDSs, will be obtained from suppliers for all new materials.
In addition, suppliers-wjll be-engaged asmecessaryrin-assessing environmental, safety and
health impacts of raw'materials, commensurate with raw materiaTrisks.
|
!?| --
/ /\ \ i
it
____________________
Product steiranish>p^ef]x>nsibilities are shared^among ESH IboduerS^wardship staff and
product stewards in each business and world area..
DSW L22343
P4-7 COMPANY CONFIDENTIAL
WATER PCB-SD0000021323
P4.4 PRODUCT HAZARD EVALUATION
P4.4.1 Introduction
Solutia's products will not present an unreasonable risk of harm to human life or health or the environment when they are properly handled, transported or used.
P4.4J2 Responsibility
ESH Product Stewardship has the responsibility for assessing hazards, if any, of chemicals that
Sohitia produces or imports. This includes evaluating the adequacy of data developed to assure
the safety and environmental aspects of products and intermediates produced in Solutia
workplaces and shipped to Solutia customers.
.'
P4.4.3 Safety and Environmental Compatibility Assessment
Each new chemical or proposed new use of an existing chemical will undergo a safety and environmental compatibility assessment Established products will be periodically reviewed to assure that their characteristics have been adequately assessed and classified and that a Material Safety Data Sheet (MSDS) exists with health and safety information. Final approval of physical and health hazard assessments will be rendered by the Leader, Product Stewardship (UPS) or designee. The L,PS will inform the Leader, Medical & Epidemiology of all assessments.
P4.4.4 Hazard Assessment
Solutia products and chemicals will be carefully evaluated for potential for human injury and environmental damage. As appropriate, ESH Product Stewardship will consider the following in performing hazard assessments:
Product and-Chcmical Name.
"\ *
*
CAS number (ifayailable)--'.
.... ,
. , ____ i
1
Common names and.synonyms
_.
--
lA\ / j_ \ \
Tradenames --- ' 5 1 ' ----- '
Molecular wetghf
Physical propeny data
Composition including known or expected impurities
--
Expected major areas of use and volume
Toxicity known
--'
Expected environmental impact from manufacturing process wastes and from product use
' and disposal
Molecular and structural formula
Countries of production and sales
P4.4.5 Hazard Determination
The Hazard Assessment will be used to make the hazard determination required by the appropriate Hazard Communication Standard and regulations (Table I). Professional judgement will be required in defining the scope of the assessment review. Computer data bases such as MSHI.MSDSARIEL Query will be used to determine the applicable regulatory requirements for Solutia products and components of Solutia products.
Continued on next page
DSW 12214*4
P4-8 COMPANY CONFIDENTIAL
WATER PCB-SD0000021324
P4A6 Material Safety Data Sheets (MSDSs)
Product Stewardship will update Solutia product and intermediate MSDSs when it becomes aware of significant new information. Supplier-provided MSDSs will be accepted as factual and will be used for employee training and for developing MSDSs for products containing these materials.
P4.4.7 Other Existing
Legal Requirements
In addition to the MSDS effort described above, some products may also be evaluated under other applicable laws such as FIFRA, TSCA, FFDCA, CEPA, EU Dangerous Substances Directives, EU Existing Substances Regulations, etc. These may require different approaches to support regulatory approval and compliance.
Table 1
Country or Region /MSDS standard or regulation
USA / OSHA Hazard Communication Standard (29 CFR 1910.1200)
EU / Commission Directive 93/112/EC
.
/ a\
1 =-V /A
filenameSoMl .doc (in;NeprahM-publicT~Tev\ 6/9/98
"^'
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Requirement Appendices A and B Annex
J)SW 1223^5
P4-9 COMPANY CONFIDENTIAL
WATER PCB-SD0000021325
Procedure PS2 Premanufacture Notification to United States Environmental Protection Agency Under The
Toxic Substances Control Act
OVERVIEW
Introduction
This section describes the company's procedure for development of premanufacture notification (PMN) to the United States Environmental Protection Agency (USEPA) as required under Section 5 of the Toxic Substances Control Act (TSCA).
Requirements Abstract
A PMN is required to be submitted to USEPA for all new < before the substance can be manufactured for commercial purposes.
NOTE: A number of substances are exempted from these requirements including, but not limited to.
drugs, food and food additives, pesticides, |-------- -N i--------
R&D substancesT\ \ | ' ) ) j \
nonisolated intermediates, and. /^\ substances on IhcTScX inventory. /-----< \
For Further Information
When further information or clarification is required, you may contact the following:
ISSUE OWNER & TECHNICAL CONTACT; Jeffrey D. Felder, Product Stewardship, F2EC (314)674-4489
Procedure Approval
This procedure was approved by
Continued on next page
CP4-1
OSW 122346
COMPANY CONFIDENTIAL
WATER PCB-SD0000021326
OVERVIEW, Continued
In This Procedure
The following areas are covered in this procedure:
Areas CP4.1 PMN REQUIREMENTS CP4.2 PMN PROCESS CP4J FOLLOWUP ON A PMN CP4.4 RESPONSIBILITIES
SeePage
CP4-3 CP4-5 CP4-S CP4-10
CP4-2
OSH L22342
COMPANY CONFIDENTIAL
WATER PCB-SD0000021327
CP4.1 PMN REQUIREMENTS
CP4.L1 Introduction
This section describes the various requirements for the development of premanufacture notifications.
CP4.1.2 PMN Determination
Checks
At a very early stage of new product development, including isolated intermediates and new imports, several checks should be made to determine if a PMN will be required for the product These checks include determining if the product is
exempt under TSCA, or
.
'new" under TSCA.
CP4.U Exemptions
CP4.1.4 Exemption ( References '
Section 2(b) of.TSCA exempts broad classes of substances such as pesticides, food, food additives, mixtures and others.
The PMN rule exempts
small quantities for R&D purposes,
substances for test marketing low volume and polymer manufacture,
impurities,
some byproducts,
.
some articles, and
nonisolated intermediates. .
I ' \|
) ! /A\ i f
j | r\
Refer to-TSCA law and regulations'onhc company's PMN manuaTfbtdctails or contact
the brainesimiirPtoduct Stewardship Manager, or ^ ^
the Leader, Product Stewardship (UPS).
-
.-
CP4.1.5 TSCA NonConfidendai Inventory
To determine if the substance is "new" under TSCA, the Product Stewardship ManagefsSbulT' search the TSCA nonconfidential inventory for the substance.
If the substance is on the TSCA nonconfidential inventory, it is not new under TSCA definition and a PMN is not required.
CP4.1.6 TSCA Confidential Inventory
If the substance in question is not on the nonconfidential inventory, the confidential inventory must be searched.
To Search the confidential inventory, a Bom Fide Intent to Manufacture (BIM) notice must be submitted to USEPA. A copy of the instruction for submitting a BIM can be found in 40CFR720.25. Send a copy of the BIM to the L,PS for corporate recordkeeping purposes.
CP4.1.7 New Substances
If USEPA reports that the substance is not on the confidential inventory, then the substance is a new substance under TSCA and a PMN is required unless the material is exempt under Section 4.1.3.
CP4-3
. Continued on next page OSH .122348
COMPANY CONFIDENTIAL
WATER PCB-SD0000021328
CP4.1 PMN REQUIREMENTS, Continued
CP4.1J Contacts Listed
Each PMN will identify a technical contact in addition to an authorized official. The technical contact will typically be
a commercial development representative,
an R&D contact, or
l*
. the business unit's Product Stewardship Manager.
CP4.1.9 Submission Timing
The PMN must be submitted to USEPA at least 90 days before the product can be manufactured for commercial purposes, including test marketing.
c
CP4-4
J>SW 122349
COMPANY CONFIDENTIAL
WATER PCB-SD0000021329
CP42 PMN PROCESS
CP4.2J Introduction
This section details the process necessary to develop a PMN.
CP4.T2 Procedure Details
The PMN process should be integrated into the development scheme of a new project. In most cases, the PMN development will be initiated during the earliest phases of commercialization of a product
CP4.23
The following table lists the steps necessary to initiate a PMN.
Initiating a PMN
Step
Action
Business unit Product Stewardship Manager submits an ESHA document, if one has not already been submitted, to the Toxicology Group.
NOTE: See ESHA Procedures.
Business unit Product Stewardship Manager drafts a PMN using USEPA form.
Business unit Product Stewardship Manager calls a scoping meeting,
consisting of, at a minimum,
the business unit contact/Product Stewardship Manager,
. the business unit technical contact,
j--an aquatic toxicologist^-. ----------j,----------- -
aTnammaliamoxicolbgist, and i L
theLP,S. ---V //\ \ i 1
>t
Copies'of tlMrPMNrirafts, along* with approved~ESHA for the substance are supplied to the participants in advance.
NOTE: The scoping meeting can be bypassed at the discretion of the business
unit Product Stewardship Manager.
_
A scoping meeting is held with decisions made by the business unit Product Stewardship Manager regarding the scope and detail of optional information to supply, the need for an optional risk analysis and, if desired, assignments to
toxicology, industrial hygiene, etc, and the need for an ESHA before PMN submission.
NOTE: It is appropriate at this stage of product development to initiate a Material Safety Data Sheet (MSDS) and a TF-837 for label and freight classification. -iv-
Continued on next page
CP4-5
DSW 122350
COMPANY CONFIDENTIAL
WATER PCB-SD0000021330
CP4.2 PMN PROCESS, Continued
CP4.2.4
The following table lists the steps involved in finalizing a PMN:
Finalizing a PMN
Step .
Responsible Person(s)
Action
1 Business unit Product Prepares final draft using input from the scoping Stewardship Manager meeting as well as followup input from Toxicology.
2 Business unit Product Reviews final draft for confidential information,
Stewardship Manager
and
with patent department Develops appropriate confidentiality claims with
representative
substantiation, where necessary. --
3 Scoping meeting participants
Circulate final draft for review.
4 Business unit Product Calls meeting for final comments/approvals, if Stewardship Manager needed.
CP4^5
PMN Information Required
The required PMN information falls into the category of either Genera] Information or Risk
Assessment Data. USEPA will accept additional data. To assist USEPA with their
assessment, in manycases irirdesirabie,orsubmit
rQJTl ^;* /A\ I
rideanalysis, ' j j j -- ^ /
pollutiohprcvcntlondata, ort
/^
L LJ
other information.
if
>0
Since the company performs a risk analysis on all new products via the Commitment Manual
and the ESHA procedures, the information is available for this purpose.
CP4J.6 PMN Information References
Final rules detailing PMN requirements can be found in 40CFR720. All PMNs must be
submitted on USEPA Form 7710-25 (5/95). Copies of this form and instructions for its use are
available from the L.PS.
.
CP4.2.7
After final review/approval, the business unit Product Stewardship Manager forwards the PMN
PMN
to the business unit Director of Technology (authorized official) for submission.
Submissions
'' The submission will include both confidential and nonconfidential PMNs using applicable
USEPA requirements. A copy ofeach will be provided to the L^PS for recordkeeping
purposes.
Continued on next page
CP4-6
DSW L2Z35.1
COMPANY CONFIDENTIAL
WATER PCB-SD0000021331
CP4.2 PMN PROCESS, Continued
CP4.2J PMN Fees
A $2500 fee, sent to a separate USEPA office from where the PMN is sent, is required for all
PMNs. Exceptions are
.
intermediates filed at the same time as the final product ($1,000 fee), or
exemptions (zero cost).
I
A unique six-digit TS-user fee identification must
be assigned to each PMN, and
appear on the check.
CP4-7
DSW .122352
COMPANY CONFIDENTIAL
WATER PCB-SD0000021332
CP43 FOLLOWUP ON A PMN
CP4J.1 Introduction
This section describes how PMN followup is handled.
CP4J3
The USEPA may
USEPA Followup
extend the review period by an additional 90 days,
ask for more information under Section 5(e),
issue a jointly agreed upon consent order which can include restrictions on manufacture or use in lieu of information, and
restrict manufacture or use under Section 5(f).
CP4.3-3 Company Followup
CP43.4 Notice of Commence to Manufacture (NCM)
The company may
request USEPA to stop the clock on PMN reviews at any time during the review period, and
commence manufacturing at any time after the USEPA review period expires, subject to any 5(e) or 5(f) restrictions.
A NoticeafCpmmemxh)Uam^dcturepjlCM) musrbe'submittedj(o USEPA within 30days of
the first-manufacture for commercial purposes. I ____;
'--J\ I i i//--. \! i
^
The informatiomoixrincluded iirtherrotice brdetaiJed in 40CFR720.
Confidential claims must be made again at this time, as appropriate.
Send a copy of the NCM to the LJPS for corporate recordkeeping purposes.
_
Once an NCM is filed with the USEPA, the PMN substance is placed on the TSCA inventory.
Continued on next page
CP4-8
XISW 122353
COMPANY CONFIDENTIAL
WATER..PCB-SD0000021333
CP43 FOLLOWUP ON A PMN, Continued
CP4-3-5 Phone Contact
All calls from the USEPA will be handled as follows: '
Call Content
Response/Action
Non-confrdential inquiries Confidential inquiries
All verbal responses
Discuss at time of call, or defer to obtain answer if unknown or if unsure of USEPA's authority in asking question.
Follow up with written response when deemed appropriate.
Discuss at discretion of techniral contact if inquiry was
previously discussed with USEPA or claimed confidential in
the PMN.
Address all other verbal confidential inquiries by written
response only.
'
.
Follow up, at technical contact's discretion, with written
letter documenting conversation and indicating areas of
confidentiality.
Give copy to L*PS.
--
CP4-9
DSW 122354
COMPANY CONFIDENTIAL
WATER PCB-SD0000021334
CP4.4 RESPONSIBILITIES
CP4.4.1 Introduction
This section describes responsible parties and responsibilities involved in the PMN process.
CP4.4.2 Responsible
Parties and Responsibilities
The following table describes persons involved in the PMN process and their responsibilities.
Responsible Party
Responsibilities
.
Business Unit Product . Stewardship Manager
Determines if product is - exempt under TSCA, - on TSCA non-confidential inventory, or - on TSCA confidential inventory.
Receives information regarding PMN, Drafts a PMN, Calls and makes decisions at scoping meetings, Prepares and reviews PMN final drafts, Forwards PMN to the DRM, TSCA, and Follows up on the PMN submission.
'
Business Unit Director, Technology
Serves as company's authorized official, and __ -x Submits-PMNs to USEPX:---- !1----------- !
j j ! Revjgws ancf approves all PMNs, | j
- * J Servesias reference for details regardingPMNs;
ReceivercSpies of BIMs for corporate recordkeeping, Serves on scoping committee, Provides PMN submission forms, Maintains copies of PMNs submitted to USEPA, and Receives copies ofNCMs for. recordkeeping.
Technical
.
Contact (as
described in
Section P4.1.S)
Receives calls from USEPA on technical matters,
Documents conversations with USEPA and forwards copies to
L,PS, and
Determines if written responses to USEPA conversations are
necessary.
-
fiicname:Pcom4.doc fin Neman M-orivatel rev. 6/9/98
CP4-I0
OSH L22353
COMPANY CONFIDENTIAL
WATER PCB-SD0000021335
Procedure PS3 Recording Allegations of Significant Adverse Reactions
Under the Toxic Substances Control Act
OVERVIEW
Introduction
This section describes the company's procedure for handling the Recordkeeping Requirements of the United States Environmental Protection Agency's (USEPA) Final Rule Under Section 8(c) of the Toxic Substances Control Act (TSCA). Similar requirements in other nations are referenced.
Abstract of 40 CFR Part 717
Manufacturers And certain processors of chemical substances and mixtures must maintain records of significant adverse reactions to health or the environment alleged to have been caused by a substance, mixture, article, process, effluent or emission. These records are subject to USEPA inspection. (Reference: 40 CFR Part 717-48 FR 38178August 22,1983)
NOTE: The Rule does not apply to pesticides, food, food additives, drugs or cosmetics when manufactured, processed or distributed only for these uses.
For Further Information
When further information or clarification is required, you may contact the following:
p
ISSUE OWNER. it technical Contact
JeffreynCFelder, Product Stewardship^ E2EG
(314)674^89 j_
Lj \Au u
u
Procedure Approval
This procedure was revised and approved by
Continued on next page
CP3-1
OSH 122356
COMPANY CONFIDENTIAL
WATER PCB-SD0000021336
OVERVIEW, Continued .
In This Procedure
The following procedures are covered in this section:
Procedures
CP3.1 ADVERSE REACTION ALLEGATIONS HANDLING CP3.2 HEALTH AND ENVIRONMENTAL ALLEGATIONS
HANDLING CP3.3 LITIGATION CLAIMS APPENDIX CP3-A - Reporting Form for Allegations of Significant Adverse Reaction to Health APPENDIX CP3.B - Flow Diagram of Solutia Procedure for Handling Allegations Subject to TSCA 8(c) APPENDIX CP3.C - TSCA 8(c) Review Procedure ofLitigation Claims
See Page CP3-3 CP3-6
CP3-9 CP3-10
CP3-11
CP3-12
CP3-2
OSW 12235?
COMPANY CONFIDENTIAL
WATER PCB-SD0000021337
CP3.1 ADVERSE REACTION ALLEGATIONS HANDLING
CP3.1.1 Introduction
CP3.L2 Definitions
This section describes the procedure for handling allegations of adverse reactions under TSCA.
The table below defines terms used in this procedure. (See Section 717.3 of the Rule for a complete listing of definitions.)
Term
Definition
Allegation
Known human effect
A statement made without formal proof or regard for evidence.
NOTE: In this instance, the alienation infers that a chemical substance or mixture has caused a significant adverse reaction to health or the environment.
A commonly recognized human health effect of a particular substance
or mixture described in:
*
scientific articles or publications abstracted in standard reference
sources, or
the firm's product labeling or material safety data sheets (MSDS).
Significant adverse reaction
NOTE: An effect is not a "known human effect" if it meets anv of the
following criteria:
significantly more severe toxic effect than previously described,
_ manifestation ofa toxiceffect aftcr-aaignificantly shorter exposure
nN period'or exposure level,thamiescriberf,,, or
; manifestation ofa toxic effect by an expbsureroute different from
j that described,--, \ j |
jj
Reactions that may indicate a substantia] impairment ofjiormal activities, or_ long lasting or irreversible damage to health or the environment
CP3.1J Rule Exemptions
The following are exemptions from the Rule that relate to the company: Activities involving solely mining or other extractive functions,
* Significant adverse reactions that are known human effects, and
Significant adverse reactions to the environment directly attributable to incidents of environmental contamination that have been reported to the United States federal government under any applicable authority.
Continued on next page
CP3-3
DSW 122358
COMPANY CONFIDENTIAL
WATER PCB-SD0000021338
CP3.1 ADVERSE REACTION ALLEGATIONS HANDUNG, Continued
CP3.1.4 Allegation Receptors
Because allegations cancome from a variety of sources including employees, contractors,
customers and neighbors, the company's receiving network must be broad. Initial receptors
include
.
plant, laboratory and other company location supervision,
plant and other company location managers,
the company's medical community at all locations, %
the business unit ESH liaisons,
'
sales and marketing contacts,
switchboard operators at all locations, and
environmental network contacts.
CP3.1.5 Key Contacts
Each domestic plant or other company-designated domestic location or laboratory will have at least one identified and trained TSCA Section 8(c) key contact Key contacts for the general offices will be
the business unit Product Stewardship liaison, and
Qro>~V
* the director of gradual iStawuuljliip (DPS), ar-designee.------- : -
/inMn! / a \ h--h re.
.
J 'The busmesstimt Product Stcwards'hipiiaisoh has thejcsponsibilityunder this procedure for
free-standingdiyisions^hd subsidiaries efwhichithe company
owns 50 percent or more of the voting stock or other equity rights, or
* has power to control the management and policies of the firm.
CP3.1.6 Recordkeeping
The TSCA Section 8(c) file will be kept in the Office of the Director, Product Stewardship. The file structure will conform to requirements of Section 717.15 of the Rule.
CP3.1.7
Hies pertaining to adverse reactions to health of employees will be retained for 30 years.
Record Retention
Hies pertaining to other adverse reactions will be maintained for five years. .
Continued on next page
CP3-4
DSW 1.2235S
COMPANY CONFIDENTIAL
WATER.P CBS60000021339
CP3.1 ADVERSE REACTION ALLEGATIONS HANDLING, Continued
CP3.1JJ
Disposition of written allegations will be communicated back to the individual making the
Communications allegation. The key contact will facilitate the communication.
A summary of the TSCA Section 8(c) procedure will be periodically
communicated to all affected employees, and
updated as appropriate.
CP3.1.9 Recording Oral Allegations
Solutia Form 8(c)A (shown as Appendix CP3-A) is available to be used for all employee related oral allegations of health effects and can be used at the discretion of the business unit Product Stewardship Liaison for external oral health allegations.
All key contacts must note the date of receipt on a written allegation.
CP3-5
OSH 122360
COMPANY CONFIDENTIAL
WATER PCB-SD0000021340
CP3-2 HEALTH AND ENVIRONMENTAL ALLEGATIONS HANDLING
CP3^.1 Introduction
This section describes the procedure for handling health or environmental allegations. This procedure is further shown on a flowchart in Appendix CP3.B.
rpX'Ll Review and Decision Process
The company's Toxic Substances Control Act (TSCA) Section 8(c) procedure consists of a four-step review and decision process as detailed in the following table.
NOTE: A determination that an allegation is not recordable under the Rule can be made at any step in the process.
Step
Action
.
1 Initial receptors will transfer to the key contact at their location * persons making oral allegations, and * 'Written allegations.
Decisions regarding the disposition of allegations are made according to the following table:
If_ and ~
then _
the initial receptors are the members of either the allegation Occupational Medicine is oral
group-(physiciaiis)-Qc the business unit:--n \ M ** < 'Product Stewardship' / /ii\ -Liaison_/y | ; j ;
!
these individuals may judge at Step One if the allegation is excluded.
i! -
/ft
U^
_U _
the decision is made that the allegation is excluded
the allegation is oral or written
it will not be acted on under this
procedure.
the allegation is not excluded
the allegation is oral
the key contact will inform the alleger that such allegation may be recordable under the Rule, and request that the alleger submit a written and signed allegation to the key contact.
Continued on next page
CP3-6
DSW 122361
COMPANY CONFIDENTIAL
WATER PCB-SD0000021341
CP3.2 HEALTH AND. ENVIRONMENTAL ALLEGATIONS HANDLING,
Continued
CP3^2
Review and Decision Process (con't)
Step
Action
2 The key contact at a location or the appropriate business unit Product Stewardship Liaison or DPS for the general offices will provide company employees with Form 8(c)A for oral allegations. The written allegations will then be reviewed by a key contact who will make a decision according to the following table:
. If-
and --
then --
the allegation is written
the allegation is exempt from it will be discarded. the Rule
the allegation is not exempt
it will be sent to the appropriate business unit Product Stewardship Liaison for review.
3 The business unit Product Stewardship Liaison will review allegations received from location key contacts and general office key contacts. If the allegation is not recordablff upder the Rule, it.wiU be discarded" ;
Continued on next page
CP3-7
0sw 122362
COMPANY CONFIDENTIAL
WATER PCB-SD0000021342
CP3.2 HEALTH AND ENVIRONMENTAL ALLEGATIONS HANDLING,
Continued
CP322 Review and Decision Process
Step `
Action
4 The Director, Product Stewardship (DPS), will form a committee to make decisions with respect to allegations that must be recorded under the Rule.
This committee will be chaired by the DPS and consist of the appropriate members of OM director for human effects, -Toxicologists for human effects, Environmental scientists for environmental effects, and Environmental Law.
Step 4 decisions will be made according to the following table:
If- then._
and --
the allegation is not
recordable under
the Rule
^
the allegation will be discarded
"< /.\ ! !L-
the business unit Product Stewardship Liaison will .provide feedback to the - -location key contact..
"the aillegation;^ -- 'thcDPSiwill place-the j
recordable wider
allegationand documents[_j
the Rule
mandated by the Rule in the
TSCA Section 8(c) file and
will notify the ESH staff at
Louvain-La-Neuve (LLN)
and LaSalle
>>'
CP3.23 Wear-Dated Hotline
Allegations received by the Wear-Dated hotline will be handled as follows:
Step
Action
______
.
*1 Allegations received by the Wear-Dated hotline will be documented by the phone operator on a standard form.
2 The documented call will be reviewed by the Product Stewardship Liaison for TSCA 8(c) relevance.
3 The hotline allegations that are judged by the Product Stewardship Liaison as meeting TSCA 8(c) recordkeeping requirements will be forwarded to the DPS for filing. .
CP3-8
DSW 122363 COMPANY CONFIDENTIAL
WATER PCB-SD0000021343
CP33 LITIGATION CLAIMS
CP3-B.1 Introduction
CP333 Detailed Procedure
This section describes the procedure necessary to process litigation claims.
The steps for handling litigation claims are detailed below.
_________ _________________________________________
Step
Action
1 (a) Litigation complaints will be reviewed by the law department asking the following questions for relevance to TSCA 8(c) recordkeeping: * Is the claim against a Soluda product or process? * Is the produces) in question one that is covered by TSCA, i.e., other than pesticide, herbicide, food, food additive or pharmaceutical?
. Is the claim a health or environmental claim?
(b) If all criteria are met, the claim will be sent to the OM director.
2 (a) Litigation claims forwarded to the law department will be reviewed by OM
based on EPA's definitions of
,
known human effects, and
.
significant adverse reactions (40 CFR 717).
(b) OM may need to contact the environmental scientist for assistance with environmental effects or toxicologists for assistance as to human effects.
(c) Claims meeting TSCA 8(c) aiteria'Will'beTorwafded to the DPS for filing.
c<
"id)
!1 :;
t
J
i
i
||
Claims^hat
---------^V / do not meet
Ai \\ 1i `-t-----------; this^cntcria will
be
jj i1 'CX dropped'fromfurther
TSCA
review of this stepr1 " --1 !--1
1 u'
3 The DPS will request from the Law Department a copy of the complaint, abstract and answer.
4 The Law Department will forward a copy of the complaint, abstract and ansWEr to'' the DPS for filing in the TSCA 8(c) file and notify the ESH staff at LLN and LaSalle.
The complaint, abstract and answer will constitute the TSCA 8(c) recordable allegation and followup for all litigation filings.
CP333 Flow Diagram#
A flow diagram of the TSCA 8(c) process for litigation complaints appears as Appendix CP3.C.
filcnamc:Pcom3.doc fin Nepran M-private) rev. 6/9/98____________________
CP3-9
' 122164
COMPANY CONFIDENTIAL
WATER PCB-SD0000021344
TO: SITE KEY CONTACT.
Form 8(c)A 10/97
APPENDIX CP3A
REPORTING FORM FOR ALLEGATIONS OF SIGNIFICANT ADVERSE REACTION TO HEALTH
Toxic Substances Control Act, Section 8(c) 40 CFR Part 717
Name of Allegen_____________________________
Address: (If not employee)
'
_____________________________________________
Date:
/ /(mc/date/yr)
Site Location:
Site Loc. Code:
(If health effect only): M___ F_____ (check one)
Year of Birth: _
Employer (if other than Solatia): ______________________________________
DESCRIPTION
OF
ALLEGED.-**A* DYERA\SEV1 1
HEALTH ~D)
EFFECT:
/A\
------------- If--------- 1
1
1.
What
is
the
health
effect'beiirijfci Ss*\Ss-
aim__edi ?/
/
:
! i / <--\ \ 1 !
1
2. How long did it last?.
3. How often have you experienced effect? __________________________________________
4. In what way did it affect your normal activities? ___________________________________
5. How were you exposed?
What substance, mixture, process or operation do you think caused the effect you described:
Signature________________________________________________________________________________ __________ For company use only:
Received on:_______________
By:__________________________
-OSW 122365
CP3-10
COMPANY CONFIDENTIAL
WATER PCB-SD0000021345
APPENDIX CP3.B
Flow Diagram of Solutia Procedure for Handling Allegations Subject to TSCA 8 (c)
CP3-11
DSV4 122366
COMPANY CONFIDENTIAL
WATER PCB-SD0000021346
APPENDIX CP3.C TSCA 8 (c) Review Procedure of Litigation Claims
Complaint, abstrac TSCA 8(c) fila
Notify ESH staff at * LLN A LaSalla plan r
'
'' DPS
CP3-J2
DSW L2236J
COMPANY CONFIDENTIAL
WATER PCB-SD0000021347
Procedure PS4 Transmittal to the United States Environmental Protection Agency
of Substantial Risk Information Under The Toxic Substances Control Act
OVERVIEW
Introduction
This section describes the company's procedure for handling the reporting of information to the United States Environmental Protection Agency (USEPA) under the 8(e) substantia] risk section of the Toxic Substances Control Act (TSCA). Similar requirements that may exist in other nations are referenced.
Abstract of TSCA 8(e) Requirements
TSCA Section 8(e) requires that the EPA be immediately informed of any person (company) who .
* manufactures, processes or distributes in commerce a chemical substance or mixture, and
* obtains information which reasonably supports the conclusion that such substance or mixture presents a substantial risk of injury to health or the environment
For Further Information
Jeffrey D. Felder, Product Stewardship, F2EC (314)674-4489
Procedure Approval
The content of this procedure was approved by '
CP2-1
DSW 1223-68
COMPANY CONFIDENTIAL
WATER PCB-SD0000021348
CP2.1 DETAILS
CP2.1.1 Introduction
This section gives details on the company's method for handling the reporting of information to the USEPA under TSCA 8(e) and for transmitting information to other world areas that may now or in the future have similar requirements.
CP2.1.2 Reporting Responsibility
The requirements of Section8(e) of the TSCA apply to ".jmy person who manufactures, processes or distributes in commerce. * It is the company's position that the "person ' who engages in the commercial activity is only the business organization, whether a sole proprietorship, corporation, partnership or association.
CP2.1.3 Designated Company TSCA 8(e) Individuals
Company organizations that might receive TSCA 8(e) information will have a designated individual to whom such information shall be communicated. At least annually, the Leader, Product Stewardship, will publish a list of the designated individuals.
CP2.1.4 Employee Notification of 8(e)
All exempt company employees throughout the world and others so designated by their organizational unit (plant nurses, contract physicians, scientists and engineers, etc.) within organizations that might receive or have access to TSCA 8(e) information, shall
be informed of the provisions of Section 8(e), and
CP2.1.5 Information Transmittal Chain
Information of the type given in the requirements abstract and detailed by EPA in their TSCA Section 8(e) Reporting Guide dated June 1991, should follow the following information transmittal chain:
Employee submits information to supervisor,
Supervisor immediately relays information to the location or department manager,
whichever is applicable,
.
Location or department manager transmits information to the proper designated individual in the organization, and
Designated individual transmits information directly to the Leader, Product Stewardship.
CP2.1.6
It is imperative that the flow of information through this transmittal chain be rapid. In the event
Timing of
of non-availability of a member of the communication network at the time information is first
Information Flow obtained, such member should be bypassed in the interest of speed.
Continued on next page
CP2-2
-DSW 122369
COMPANY CONFIDENTIAL
WATER PCB-SD0000021349
CP2.1 DETAILS, Continued
CP2.1.7 Records of Information
All individuals involved in submission of substantial risk information to the Leader, Product Stewardship should keep a record of date ofreceipt and pertinent identifying details.
CP2.1A 8(e) Committee
The designated official 8(e) committee will make decisions with respect to information that must be reported to the EPA under Section 8(e) of the TSCA. This committee will be comprised of the following;
the Senior Medical Officer,
Lead, Product Stewardship Risk Assessment & Risk Management,
Environmental Counsel,
Leader, Product Stewardship,
'
the appropriate business unit ESH Business Liaison and/or Product Stewardship Manager, and
Additional ad hoc members may be asked to participate as circumstances may require.
CP2.1.9 Committee Decisions
Appropriate senioHnanhgement-wil] be informed ofeommittee-decisions.
, ^=1; `1 ]! --V //\\ | =: 11 ^
-
In the evfcnt that a committec oecisipnis not unanimous, the next appropriate level of managemehvshati-bc-cOnsulted andkhemattCr^will-be resolved'at tnerlughest level, if necessary.
Minutes of the meeting will be retained by the Leader, Product Stewardship who will arrange for notification of action to the submittor.
In the event that the committee decides information must be reported to EPA, ESH staff at Louvain-La-Neuve and LaSalle plant will also be informed so that they may comply with similar requirements that may exist in their world areas. The Leader, Product Stewardship will make notifications that may be required by other world areas.
CP2.1 DETAILS, Continued
CP2-3
DSM 122370
COMPANY CONFIDENTIAL
WATER PCB-SD0000021350
CP2.1 DETAILS, Continued
CP2.1.10
Employee Notification of Committee Action
Information submitted by employees will be handled according to the following table:
.
,_________
If-
and-- -
then--
.
An employee submits information
An employee submits information directly to the EPA without the company's prior knowledge
the information is submitted through company channels
the employee will be notified of action taken by the 8(e) committee and the reasons for such action.
the company has evaluated
and determined the
information is not reportable
under 8(e)
'
the company should review the situation to determine what action, if any, it should take with the EPA.
filenameiPcomZdoc (in Nepran M-privte) rev. 6/9/98
CP2-4
DSW L2237JL
COMPANY CONFIDENTIAL
WATER_PCB-SD0000021351
Procedure PS5 Transmittal of Toxicology and Health-Related Data
To United States Regulatory Agencies
OVERVIEW
CP6.1 Introduction
CP(L2 Policy
CP6-3 Test Data Submission
This section describes the policy and procedure for supplying health-related information to regulatory agencies.
Health-related information should be submitted through ESH Stewardship.
All toxicology or health-related data will be reviewed with ESH Stewardship prior to submission to any regulatory agency.
CP6.4 Homan Health Effects Data
CP6.5 Human Health Effects Data
If the submission include data on human health effects, it is preferable that the information be submitted to the regulatoryragency by theESH Toxicology Tram ,
) / A \......................................................................................Tc;
The letter Of transmiSah'foiLany toxicology ochealJth-related data musrinclude a list of the
materials being transmitted, including sufficient bibliographic information for subsequent retrieval of the original data.
Any such information transmitted must be recorded and the copy of the final submission
retained by both
--
the Leader, Product Stewardship, and
* the involved business unit.
Continued on next page
CP6-1
OSH 122372
COMPANY CONFIDENTIAL
WATER PCB-SD0000021352
Transmittal of Toxicology and Health-Related Data to United States . Regulatory Agencies, Continued
CP6.6 Regulatory Agency Agreements
CP6.7
-
Exceptions
CP6.8 For Further Information
CP6.9 Procedure Approval
Agreements with a regulatory agency that commit the company to the future transmittal of toxicology or health-related data must
' * be reviewed and approved in advance by ESH Leader, Product Stewardship,
have concurrence of ESH Leader, Product Stewardship regarding the feasibility of meeting
commitment dates, and
have appropriate records of such commitments maintained by both the involved business unit and ESH Leader, Product Stewardship in order to ensure future compliance with such agreements/
Any exceptions to the above must be approved by the Leader, Product Stewardship.
When further information or clarification is required, you may contact the following:
ISSUE OWNER: Jeffrey D. Felder, Product Stewardship, F2EC (314)674-4489
_ ..TECHNICAL CONTACT: jj / a \ i cz:
; (J LiFrederidtJtTohannsen, Product Stewardship, F2EC--'
(314)674^15 | --V |
LT~\\
The content of this procedure was approved by
filenirae:Pcon>6.doc (in Ncprcn M-private) rev. 6/9/98
CP6-2
J3SW 122373
COMPANY CONFIDENTIAL
WATER PCB-SD0000021353
OVERVIEW
Program PS6 Use of Animals in Research Facilities
Introduction Policy
For More Information
Program Approval
This program contains details of the company's policy and practices regarding the use of' animals in research facilities.
The company will ensure that all animals used on its behalf in its research programs are involved in projects of importance to society, and receive humane and professionally competent care and treatment
When further information or clarification is required, you may contact the following;
ISSUE OWNER: Frederick R. Johannsen, ESH, F2EC (314)674-8815.
___^
:------^ >, / . \
The contcnt-df t lisprograi i was-approvcd fay.
i ) i i Il//--\\ y
1---------il-- ____;
1-------1
PiS-i
OSW 122374
COMPANY CONFIDENTIAL
WATER PCB-SD0000021354
P15.1 DETAILS
P15.1.1 Introduction
This section describes the details of the company's practices regarding the use of animals in
contract research facilities.
.
P15.1.2 Background
The company
develops industrial products that are used to better the quality of human life throughout the
` world, and
.
* works to ensure that these products - provide valuable benefits to society, and - are safe to use.
P15.1J Need for Use of Laboratory Animals
In conducting research to ensure product efficacy and safety, company scientists use a variety
of new technologies, such as
'
computer models, cell culture systems, and other processes.
These technologies are used to
* identify effective products duty in the process, and
* detectpoten tiaThealth problem^ or nncleWat leiside.effects!! r~\ -
i i--1 ]l
These systems arclinyted, however, because they do not fullyjepreisenfthe complex processes of the human body. For this reason, product research and evaluation requires the use of laboratory animals.
P15.1.4 Information Requirement
The company requires all scientists, technicians and managers associated with animal rcsfi^rciL^- . programs to be fully cognizant and supportive of the specifics and spirit of this chapter.
Continued on next page
P15-2
DSW L22375
COMPANY CONFIDENTIAL
WATER PCB-SD0000021355
P15.1 DETAILS, Continued
P15.1.5 Program Supervision
The facilities contracted to support company animal research are
directed and monitored by an attending doctor of veterinary medicine, and
fully accredited by the American Association for the Accreditation of Laboratory Animal Care (AAALAQ.
P15.1.6 Research Animals Used
Since rodents account for over 90% of all research subjects, the vast majority of animals used are rabbits, rats and mice. The remainder includes dogs, pigs, sheep, cattle, goats and occasionally monkeys.
NOTE: The company does 2! contract with laboratories that buy animals from pounds or shelters.
P15.1.7 Animal Use Protocol
Since the company's goal is to give the highest consideration to the well-being of all animals used in research, it requires that contract laboratories follow these steps:
1 STEP
ACTION
`
1 Assien aircompany research animals to a snecihc orotocol under the direction of
-^'principal investigator. / A \ | i------ , j |
i / {i
\ / "' \ j =
;j
|
^Reriew-eaph protocol according to procedures prescribaLbygovernmental
regulations amTadhercd to'by the~ACUC.
NOTE: This must be done before research can commence.
3 Review and approve each protocol by an attending veterinarian and the ACUC.
4 Maintain records of research use and routine care for each animal.
Continued on next page
Pi 5-3
OSH 1223.7<*
COMPANY CONFIDENTIAL
WATER PCB-SD0000021356
P15.1 DETAILS, Continued
P1S.1J Research Facilities
The company requires that its contractors conduct all animal research in modem, wellmaintained facilities that meet or exceed all regulatory standards.
P15.1.9 Information Requests
General information on the company's policy and procedures regarding animals used in - research may be requested from Solutia ESH Communications, 10300 Olive Boulevard, P.O. Box 66760, St. Louis, Missouri 63166-6760. The telephone number is (314) 674-8552.
filename:sol15jdf.doc (in Nepran M-public) rev. 6/9/98
P15-4
osw 122377
COMPANY CONFIDENTIAL
WATER PCB-SDO000021357
DSW 122378
WATER_PCB-SDOo6o021 358
WATER PCB-SD0000021359
CROSS-REFERENCE: COMMITMENTS MANUAL AND RESPONSIBLE CARE(R) (to be written)
filename:crsref.doc (in Nepran M-private)
OSH 122380
WATER_PCB-SD0000021360
SPONSIBLE CARE
DSW 122381
WATER PCB-SD0000021361
&
W:RESPONSIBLE CARE
A Public Commitment
Guiding Principles
As a member of the Chemical Manufacturers Association, this company is committed to support a continuing effort to improve the industry's responsible management of chemicals. We pledge to manage our business according to these principles:
.
To recognize and respond to community concerns about chemicals and our operations.
To develop and produce chemicals that can be manufactured, transported, used and disposed of safely.
To make health, safety and environmental considerations a priority in our planning
for all existing and new products and processes.
.
To report promptly to officials, employees, customers and the public, information on chemical-related health or environmental hazards and to recommend protective measures.
To counsel customers on the safe use, transportation and disposal of chemical products.
To operate our plants and facilities in a manner that protects the environment and the health and safety of our employees and the public.
To extend knowledge by conducting or supporting research on the health, safety and environmental effects of our products, processes and waste materials.
To work with others to resolve problems created by past handling and disposal of hazardous substances.
To participate with government and others in creating responsible laws, regulations and standards to safeguard the community, workplace and environment.
To promote the principles and practices ofResponsible Care* by sharing experiences and offering assistance to others who produce, handle, use, transport or dispose of chemicals.
OSW 122382
WATER_PCB-SD0000021362
v
W:Responsible Care
A Public Commitment
10 Elements of Responsible Care
Guiding Principles
-
These statements ofthe philosophy ofResponsible Care outline each CMA member and
Partner's commitment to environmental, health, and safety responsibility in managing
chemicals. Members and Partners pledge to manage their businesses according to these
principles.
*
Codes of Management Practices At the heart ofthe Responsible Care initiative are the six codes of management' practices. The Codes focus on management practices in specific areas of chemical operations. Members and Partners must make continuous progress in attaining the goals of each Code.
The Community Awareness and Emergency Response (CAER) Code promotes emergency response planning and calls for ongoing dialogue with local communities.
The Pollution Prevention Code commits industry to the safe management and reduction of wastes.
The Process Safety Code is designed to prevent fires, explosions, and accidental chemical releases.
The Distribution Code focuses on reducing employee and public risks from the shipment of chemicals and applies to the transportation, storage, handling, transfer and repackaging of chemicals.
The Employee Health and Safety Code protects employees and visitors at company sites.
The Product Stewardship Code makes health, safety and environmental protection an integral part ofdesigning, manufacturing, marketing, distributing, using, recycling and disposal of products.
Public Advisory Panel A group of environmental, health and safety thought leaders assists the industry in identifying and developing programs and actions that are responsive to public concerns.
DSW 122383
WATER PCB-SD0000021363
Self-Evaluations
.
Members and Partners submit reports annually on their progress in implementing each of
the Codes. These self-evaluations provide a measure of company progress and are a
valuable management tool for CMA and individual companies in directing assistance
efforts.
Measures of Performance Recognizing the need for measurement that goes beyond self-evaluations, performance measures are being developed for each ofthe Codes. Through these measures, the industry and the public will gain a better appreciation for the progress CMA members and Partners are making in carrying out Responsible Care.
Management Systems Verification The Management Systems Verification process assists members and Partners in their management and implementation ofResponsible Care . The process provides participating companies with an external view ofthe effectiveness oftheir management systems for carrying out Responsible Care and helps demonstrate the integrity of the initiative to key audiences.
Executive Leadership Groups Senior level support for Responsible Care continues to be an essential ingredient ofthe initiative's success. Regular regional meetings provide a forum for senior executives to share experiences and take action on advancing the implementation ofResponsible Care.
Mutual Assistance
Direct company-to-company mutual assistance has surfaced as one ofthe most effective
methods for advancing Responsible Care. Members and Partners at the executive
contact. Responsible Care Coordinator, and practitioner levels regularly share
information through the mutual assistance network, often through state chemical
--
associations, which are vital to the success ofthe network.
Partnership Program The Partnership Program provides an opportunity for those who otherwise may not be eligible for membership in CMA to participate directly in the Responsible Care initiative. Companies that take ownership or possession of chemicals and chemical-related associations are eligible for membership in the Responsible Care Partnership program.
Obligation of Membership CMA Bylaws obligate member companies to participate in Responsible Care as defined by the Board. This includes ascribing to the Guiding Principles, participating in the development of the initiative and making good faith efforts to implement the program elements of the Responsible Care initiative.
OSW 122384 WATER PCB-SD0000021364
Responsible Care A Public Commitment
Community Awareness and Emergency Response Code of Management Practices
Purpose:
The goal of the Community Awareness and Emergency Response (CAER) Code of Management Practices is to assure emergency preparedness and to foster community right-to-know. It demands a commitment to openness and community dialogue. The code has two major components: first, to assure that member facilities that manufacture, process, use, distribute or store hazardous materials initiate and maintain a community outreach program to openly communicate relevant, useful information responsive to the public's questions and concerns about safety, health, and the environment; and second, to help protect employees and communities by assuring that each facility has an emergency response program to respond rapidly and effectively to emergencies.
The community outreach component will communicate program activities and performance under all codes of management practices and will promote an open, ongoing dialogue with employees and the community. Information should be provided about such activities as waste minimization, emission reduction, health effects of chemicals, and efforts to ensure the safe transport of chemicals.
The CAER Code ofManagement Practices is supported by, and will build on, CMA's CAER process. CAER supports the community's right to know about chemical industry operations and their effect on safety, health, and the environment. CAER originally was a voluntary initiative focused on emergency response issues. The new CAER Code of Management Practices broadens the facility-community dialogue to cover the full range of safety, health and environmental issues.
Relationship to Guiding Principles:
__
The Code helps achieve several ofthe Responsible Care(r) Guiding Principles:
To recognize and respond to community concerns about chemicals and our operations.
To report promptly to officials, employees, customers, and the public, information on chemical-related health or environmental hazards and recommend protective measures.
4 DSW 122385
WATER PCB-SD0000021365
To participate with government and others in creating responsible laws, regulations, and standards to safeguard the community, workplace and environment.
To promote the principles and practices ofResponsible Care(r) by sharing experiences and offering assistance to others who produce, handle, use, transport, or dispose of chemicals.
Management Practices;
A. Community Awareness and Outreach
*
Member facilities that manufacture, process, use, distribute or store hazardous materials shall have a community outreach program that includes:
For Employees:
1. An ongoing assessment of employee questions and concerns about the facility.
2. Communications training for key facility and company personnel who communicate with employees and the public concerning safety, health, and environmental issues.
3. Education of employees about the facility's emergency response plan and safety, health, and environmental programs.
4. An ongoing dialogue with employees to respond to their questions and concerns
and involve them in community outreach efforts. -
-
5. A regular evaluation of the effectiveness of the ongoing employee communications efforts.
For Community:
6. An ongoing assessment of community questions and concerns about the facility.
7. An outreach program to educate responders, government officials, the media,
other businesses and the community about the facility's emergency response
.
program and risks to the community associated with the facility.
8. A continuing dialogue with local citizens to respond to questions and concerns about safety, health, and the environment, and to address other issues of interest to the community.
3
DSW 122386 WATER PCB-SD0000021366
9. A policy of openness that provides convenient ways for interested persons to become familiar with the facility, its operations, and products, and its efforts to protect safety, health, and the environment.
10. A regular evaluation ofthe effectiveness ofthe ongoing community communications efforts.
B.Emergency Response and Preparedness
Member facilities that manufacture, process, use, distribute or store hazardous materials shall have an emergency response program that includes:
1. An ongoing assessment of potential risks to employees and local communities resulting from accidents or other emergencies.
2. A current, written facility emergency response plan which address, among other things, communications and the recovery needs of the community after an emergency.
3. An ongoing training program for those employees who have response or communications responsibilities in the event of an emergency.
4. Emergency exercises, at least annually, to test operability ofthe written emergency response plan.
5. Communication ofrelevant and useful emergency response planning information to the Local Emergency Planning Committee.
6. Facility tours for emergency responders to promote emergency preparedness and* to provide current knowledge offacility operations.
7. Coordination of the written facility emergency response plan with the comprehensive community emergency response plan and other facilities. Ifno plan exists, the facility should initiate community efforts to create a plan.
8. Participation in the community emergency response planning process to develop and periodically test the comprehensive community emergency response plan developed by the Local Emergency Planning Committee.
9. Sharing ofinformation and experience relating to emergency response planning, exercises, and the handling of incidents with other facilities in the community.
6 0SW U238J
WATER PCB-SD0000021367
Responsible Care A Public Commitment
Pollution Prevention Code of Management Practices
Purpose:
This Code is designed to achieve ongoing reductions in the amount of all contaminants and pollutants released to the air, water, and land from member company facilities. These reductions are intended to respond to public concerns with the existence of such releases, and to further increase the margin of safety for public health and the environment.
The Code is also designed to achieve ongoing reductions in the amount ofwastes generated at facilities. These reductions are intended to help relieve the burden on industry and society ofmanaging such wastes in future years.
In implementing the Code, each company should strive for annual reductions, recognizing
that production rates, new operadpns, and other factors may result in increases. Despite
these fluctuations, however, the goal is to establish a long-term, substantial downward
trend in the amount ofwastes generated and contaminants and pollutants released.
Quantitative reduction goals will be established for giving priority to those pollutants,
contaminants and wastes ofhighest health and environmental concern.
_
This code also includes practices that address the broader waste management issues ^ beyond source reduction and other waste and release reduction efforts. Each member company must manage remaining wastes and releases in a manner that protects the environment and the health and safety of employees and the public.
This Code complements, and should be implemented in conjunction with current and future Codes ofManagement Practices. Key terms are defined in the Glossary, which should be consulted for assistance in interpreting the provisions of this Code.
Relationship to Guiding Principles:
Implementation ofthis Code helps achieve the following Guiding Principles:
To recognize and respond to community concerns about chemicals and our operations.
To develop and produce chemicals that can be manufactured, transported, used and
disposed of safely.
.
7 DSW 122338
WATER PCB-SD0000021368
To make health, safety, and environment considerations a priority in our planning for all existing and new products and processes.
To report promptly to officials, employees, customers and the public, information on chemical-related health or environmental hazards and to recommend protective measures.
To operate our plants and facilities in a manner that protects the environment and the health and safety of our employees and the public.
To extend knowledge by conducting or supporting research on the health, safety, and environmental effects of our products, processes, and waste materials.
To promote the principles and practices ofResponsible Care by sharing experiences and offering assistance to others who produce, handle, use, transport, or dispose of chemicals.
To work with others to resolve problems created by past handling and disposal of hazardous substances.
To participate with government and others in creating responsible laws, regulations and standards to safeguard the community, workplace and environment.
To promote the principles and practices ofResponsible Care by sharing experiences and offering assistance to others who produce, handle, use, transport or dispose of chemicals.
Management Practices:
Each member company shall have a pollution prevention program which shall include:
1. A clear commitment by senior management through policy, communications, and resources, to ongoing reductions at each ofthe company's facilities, in releases to the air, water, and land and in the generation ofwastes.
2. A quantitative inventory at each facility ofwastes generated and releases to the air, water, and land, measured or estimated at the point ofgeneration or release.
3. Evaluation, sufficient to assist in establishing reduction priorities, ofthe potential impact ofreleases on the environment and the health and safety of employees and the public.
4. Education of and dialogue with, employees and members of the public about the inventory, impact evaluation, and risks to the community.
X)SW 122389
WATER_PCB-SD0000021369
Establishment ofpriorities, goals and plans for waste and release reduction, taking into account both community concerns and the potential health, safety, and environmental impacts as determined under Practices 3 and 4.
Ongoing reduction ofwastes and releases, giving preference first to source reduction, second to recycle/reuse, and third to treatment. These techniques may be used separately or in combination with one another.
Measurement ofprogress at each facility in reducing the generation ofwastes and in reducing releases to the air, water, and land, by updating the quantitative inventory at least annually.
Ongoing dialogue With employees and members ofthe public regarding waste and release information, progress in achieving reductions, and future plans. This dialogue should be at a personal, face-to-face level, where possible, and should emphasize listening to others and discussing their concerns and ideas.
Inclusion ofwaste and release prevention objectives in research and in design of new or modified facilities, processes, and products.
An ongoing program for promotion and support ofwaste and release reduction by
others, which may, for example, include:
.
a. Sharing of technical information and experience with customers and suppliers;
b. Support of efforts to develop improved waste and release reduction techniques;
c. Assisting in establishment of regional air monitoring networks;
d. Participation in efforts to develop consensus approaches to the evaluation of environmental, health, and safety impacts of releases;
e. Providing educational workshops and training materials;
.
f. Assisting local governments and others in establishment ofwaste reduction programs benefiting the general public.
Periodic evaluation ofwaste management practices associated with operations and equipment at each member company facility, taking into account community concerns and health, safety, and environmental impacts and implementation of ongoing improvements.
9 OSH 122390
WATER PCB-SD0000021370
12. Implementation of a process for selecting, retaining, and reviewing contractors and toll manufacturers taking into account sound waste management practices that protect the environment and the health and safety of employees and the public.
13. Implementation of engineering and operating controls at each member company facility to improve prevention of and early detection ofreleases that may contaminate groundwater. -
i
14. Implementation ofan ongoing program for addressing past operating and waste management practices and for working with others to resolve identified problems at each active or inactive facility owned by a member company taking into account community concerns and health, safety, and environmental impacts.
Industry Trend Data:
To develop and maintain statistical industry trends, CMA will collect currently available data. Each company shall report annually to CMA, or its designated agent, for each facility: Releases of substances as reported under SARA Section 313; and Wastes generated, as defined and reported in CMA's annual waste survey.
10 su L239li
WATER PCB-SD0000021371
responsible Care A Public Commitment
Process Safety Code of Management Practices
Purpose:
The Process Safety Code is designed to prevent fires, explosions and accidental chemical releases. The Code is comprised ofa series ofmanagement practices that reflect this goal, with the expectation of continuous performance improvement for each management practice. The practices are based on the principle that facilities will be safe ifthey are designed according to sound engineering practices, built, operated and maintained properly and periodically reviewed for conformance.
Process safety is an interdisciplinary effort. Consequently, the Code is divided into the
following four elements: management leadership, technology, facilities and personnel.
Each element is composed ofManagement Practices. Individually, each Practice describes
an activity or approach important to preventing fires, explosions and accidental chemical
releases. Collectively, the Practices encompass process safety from the design stage
through operation, maintenance and training. The scope ofthis Code includes
manufacturing, processing, handling and on-site storage of chemicals. This Code must be
implemented with full recognition of the community's interest, expectations and
participation in achieving safe operations.
.
The process safety management program in each facility is complemented by workplace health and safety programs, as well as waste and release reduction programs which address and minimize releases and waste generation. These three programs, and others, will help assure that CMA member facilities are operated in a manner that protects the environment and the health and safety of personnel and the public.
Relationship to Guiding Principles:
The Code helps achieve several ofthe Responsible Care Guiding Principles:
To recognize and respond to community concerns about chemicals and our operations.
To make health, safety and environmental considerations a priority in our planning for
all existing and new plants and processes.
.
11 DSW 122392
WATER PCB-SD0000021372
To operate our plants and processes in a manner that protects the environment and the health and safety of our employees and the public.
Management Practices:
Each member company shall have an ongoing process safety program that includes:
Management Leadership
1. Leadership by senior management through policy, participation, communications and resource commitments in achieving continuous improvement of performance.
2. Clear accountability for performance against specific goals for continuous improvement
3. Measurement ofperformance, audits for compliance and implementation of . corrective actions.
4. Investigation, reporting, appropriate corrective action and follow-up of each incident that results or could have resulted in a fire, explosion or accidental chemical release. -
5. Sharing of relevant safety knowledge and lessons learned from such incidents with industry, government and the community.
6. Use ofthe Community Awareness and Emergency Response (CAER) process to assure public comments and concerns are considered in design and implementation of the facility's process safety systems.
Technology:
.
7. Current, complete documentation ofprocess design and operating parameters and
procedures.
.
8. Current, complete documentation ofinformation relating to the hazards of materials and process technology.
9. Periodic assessment and documentation ofprocess hazards, and implementation of actions to minimize risks associated with chemical operations, including the possibility ofhuman error.
10. Management of changes to chemical operations to maintain or enhance the safety originally designed into the facility.
12 JDSW 122393
WATER PCB-SD0000021373
Facilities:
11. Consideration and mitigation of the potential safety effects of expansions, modifications and new sites on the community, environment, and employees.
12. Facility design, construction and maintenance using sound engineering practices consistent with recognized codes and standards.
13. Safety reviews on all new and modified facilities during design and prior to start -up.
14. Documented maintenance and inspection programs that ensure facility integrity.
15. Sufficient layers of protection through technology, facilities and employees to prevent escalation from a single failure to a catastrophic event.
16. Provision for control ofprocesses and equipment during emergencies resulting from natural events, utility disruptions and other external conditions.
Personnel:
.
17. Identification ofthe skills and knowledge necessary to perform each job.
18. Establishment ofprocedures and work practices for safe operating and maintenance activities.
19. Training for all employees to reach and maintain proficiency in safe work practices and the skills and knowledge necessary to perform their job.
20. Demonstrations and documentation of skill proficiency prior to assignment to independent work, and periodically thereafter.
21. Programs designed to assure that employees in safety critical jobs are fit for duty and are not compromised by external influences, including alcohol and drug abuse.
22. Provisions that contractors either have programs for their own employees consistent*with applicable sections ofthis Code or be included in the member company's program, or some combination ofthe two.
13
DSW 122394
WATER PCB-SD0000021374
Glossary
This Code uses key terms in a context that may be broader than their associated regulatory definitions. However, adherence to this Code does not relieve a company ofthe obligation to meet Federal, state and local regulatory requirements.
Process Safety - The application ofmanagement and engineering principles to prevent fires, explosions and accidental chemical releases at chemical process facilities.
Sound Engineering Practice - The application ofmandatory codes and standards
supplemented by the use ofvoluntary codes, standards and guidelines, tempered by
professional judgment.
.
Safety Critical Jobs - Jobs, activities and tasks, if improperly performed, that have the
potential to significantly increase the risk ofa fire, explosion or accidental chemical
release.
.
Accidental Chemical Release - Unplanned, sudden releases ofchemicals from manufacturing, processing, handling and on-site storage facilities to the air, water or land. It does not include permitted or other releases.
14
DSW 1223*5
WATER_PCB-SD0000021375
Responsible Care A Public Commitment
Distribution Code of Management Practices
Purpose;
The purpose ofthe Distribution Code ofManagement Practices is to reduce the risk of harm posed by the distribution of chemicals to the general public; to carrier, distributor, contractor and chemical industry employees; and to the environment. Adherence to the code will lead to continually safer chemical distribution and help member companies to: evaluate the risks associated with chemical distribution and methods to reduce those
risks; meet or exceed all regulations and industry standards governing chemical distribution; provide emergency advice and/or assistance to people on the scene in the event of a
chemical distribution emergency, develop new technologies and methods to improve chemical distribution safety. The code will also promote improvements in: employee preparedness and awareness in preventing distribution emergencies; the safety performance of carriers and other providers of distribution services; the public's preparedness in responding to chemical distribution emergencies; the public's understanding of and confidence in, industry efforts to improve chemical
distribution safety.
15 DSW 1223-96
WATER PCB-SD0000021376
The Distribution Code ofManagement Practices applies to all modes oftransportation (highway, rail, marine, air and pipeline) and to the shipment of all chemicals, including chemical waste. The code also applies to distribution activities (storage, handling, transfer and repackaging) while chemicals are in transit between member companies and their suppliers and customers. The implementation of a number of practices ofthe code will vary according to the characteristics ofthe chemical being distributed, the mode of transportation and the type of distribution activity involved.
Relationship to Guiding Principles:
This code helps achieve several Responsible Care Guiding Principles:
To recognize and respond to community concerns about chemicals and our operations;
To make health, safety and environmental considerations a priority in our planning for all existing and new products and processes;
To counsel customers on the safe use, transportation, and disposal of chemicals;
To operate our plants and facilities in a manner that protects the environment and the health and safety of our employees and the public;
To participate with government and others in creating responsible laws, regulations and standards to safeguard the community, workplace and environment; and ???????
To promote the principles and practices ofResponsible Care by sharing experiences
and offering assistance to others who produce, handle, use, transport or dispose of
chemicals.
.
Management Practices:
Each member company shall have an ongoing chemical distribution safety program that includes senior management commitment through policy, communications and resources to improvements in chemical distribution safety. The program should include the following elements:
1. Risk Management
1.1 Regular evaluations of chemical distribution risks which consider the hazards of the material, the likelihood of accidents/incidents and the potential for human and environmental exposure from release ofthe material over the route oftransport.
1.2 Implementation of chemical distribution risk reduction measures that are appropriate to the risk level.
.
16 122397
WATER_PCB-SD0000021377
1.3 Internal reporting and investigation of chemical distribution accidents/incidents, and implementation ofpreventive measures.
2. Compliance Review and Training
2.1 A process for monitoring changes and interpretations ofnew and existing regulations and industry standards for their applicability to the company's chemical distribution activities, and for implementing those regulations and standards.
2.2 Training for all affected company employees in the proper implementation of' applicable regulations and company requirements.
2.3 A program for providing guidance and information to carriers, distributors and
contractors who perform distribution activities for the company on the company's
training and compliance requirements for the activities.
'
2.4 Regular reviews of company employee, carrier, distributor and contractor compliance with applicable regulations and company requirements.
3. Carrier Safety
'
3.1 A process for qualifying carriers ofall modes and types (common, contract, private and customer controlled) that transport chemicals to and from company facilities that emphasizes carrier safety fitness and regulatory compliance, and includes regular reviews of their performance and compliance.
3.2 Feedback to carriers on their safety performance and suggestions for improvement.
4. Handling and Storage
--* .
4.1 Documented procedures for the selection and use of containers that are appropriate for the chemical being shipped, in compliance with testing and certification requirements, and free ofleaks and visible defects.
4.2 Documented procedures for loading chemicals at company facilities that will reduce emissions to the environment, protect personnel and provide securement of the ladinglduring transit.
4.3 Documented procedures for unloading chemicals at the company's facilities that will reduce emissions to the environment, protect personnel, and provide for safe unloading into proper storage facilities.
4.4 Defined criteria for the cleaning and return of tank cars, tank trucks, marine
vessels, and retumable/refillable bulk and semi-bulk containers, and for the proper
disposal of cleaning residues.
.
17
DSW 122398
WATER PCB-SD0000021378
4.5 A program for providing guidance and information to customers, distributors, and
other receivers on proper procedures for unloading and storing the company's
chemicals.
-
4.6 A process for selecting distributors and other facilities that store or handle the company's chemicals in transit that emphasizes safety fitness and regulatory compliance and includes regular reviews oftheir performance and compliance.
4.7 Feedback to distributors and operators of other facilities that store or handle . chemicals in transit on their safety performance and suggestions for improvement.
5. Emergency Preparedness
5.1 A process for responding to chemical distribution accident/incidents involving the
company's chemicals.
.
5.2 Documented procedures for making information about the company's chemicals in distribution available to response agencies.
5.3 A program for making facilities and/or training materials available to emergency
response agencies. .
.
5.4 Dialogue with state and local emergency planning organizations on the distribution
and hazards ofthe company's chemicals to improve community preparedness to
respond to chemical distribution emergencies.
'
5.5 Dialogue with the public on their concerns about chemical distribution safety, actions taken by the industry and the company to improve the safety of chemical distribution, and the effectiveness of emergency preparedness and emergency --< response assistance.
18 DSW L2239U9
WATER PCB-SD0000021379
wsi, Responsible Care A Public Commitment
Employee Health and Safety Code of Management Practices
Purpose:
The goal of the Employee Health and Safety Code ofManagement Practices is to protect and promote the health and safety of people working at or visiting member company work sites.
To achieve this goal, the Code provides Management Practices designed to continuously improve work she health and safety. These practices provide a multidisciplinary means to identify and assess hazards, prevent unsafe acts and conditions, maintain and improve employee health, and foster communication on health and safety issues.
Implementation ofthe Employee Health and Safety Code, together with other Codes of Management Practices, can enable member companies to operate in a manner that further protects and promotes the health and safety of employees, contractors, and the public, and protects the environment.
Relationship to Guiding Principles:
_
_
Implementation ofthe Code helps achieve several ofthe Responsible Care Guiding --* Principles:
To recognize and respond to community concerns about chemicals and our operations.
To make health, safety, and environmental considerations a priority in our planning for all existing and new products and processes.
To operate our plants and facilities in a manner that protects the environment and the health and safety ofour employees and the public.
To extend knowledge by conducting or supporting research on the health, safety, and environmental effects of our products, processes, and waste materials.
05w 122400
WATER PCB-SD0000021380
Management Practices:
Each member company shall have an ongoing occupational health and safety program that includes:
Program Management
1. Commitment by all levels of management to protecting and promoting the health and safety of people working at or visiting member company work sites, through: published policies; accountability for implementation; and provision of sufficient resources, including qualified health and safety personnel.
2. Opportunities for employees to participate in developing, implementing, and reviewing health and safety programs.
3. Provisions, including selection criteria, to confirm that on-site contractors* programs are consistent with applicable Management Practices of this Code.
4. Written, up-to-date health and safety programs and procedures appropriate to the facility.
5. Means to verify that health and safety programs and procedures are effective and that actual practices are consistent with these programs and procedures.
6. Systems for maintaining records and analyzing data to evaluate health and safety performance, determine trends, and identify areas for improvement.
Identification and Evaluation:
7. Methods to identify and evaluate potential health and safety hazards in planned or ~ existing facilities, including facilities to be modified.
8. Exposure assessments and safety analyses to evaluate health and safety hazards to employees from processes; equipment; potentially hazardous chemical, physical, or biological agents; or other work site conditions.
9. Health assessments to determine employee medical fitness for specific job tasks.
10. Employee occupational medical surveillance programs tailored to work site
hazards.
.
.OSW 122401
WATER PCB-SD0000021381
Prevention and Control:
11. Mechanisms for reviewing the design and modification offacilities and job tasks, taking into account the following hierarchy of controls: inherent safe design, material substitution, engineering controls, administrative controls, and personal
protective equipment
12. Systems to verify that health and safety equipment is properly selected, maintained, and used.
13. Preventive maintenance and housekeeping programs to maintain the safety of facilities, tools, and equipment
14. Timely investigation ofwork site illnesses, injuries, and incidents; corrective actions to prevent recurrence; and evaluation ofthe effectiveness ofcorrective actions taken.
15. Security procedures and systems to control entry and exit ofpersonnel and materials at the work site and restricted areas.
16. Provisions for emergency medical assistance for people at work sites.
Communications and Training:
17. Communication ofhealth and safety information that is relevant to specific job tasks and the work rite.
18. Health and safety training programs, including documentation of these"programs, and methods to evaluate the effectiveness ofboth training and communications ^ activities.
Trend Industry Data:
To identify industry trends, each company shall report to CMA, or its designated agent, occupational injuries and illnesses, as specified in CMA's Occupational Injury and Illness Reporting Program.
Relationship to Other Codes of Management Practices:
This Code complements, and should be implemented in conjunction with, current and future Codes ofManagement Practices, especially those elements ofthe CAER Code involving emergency response, the Process Safety Code involving training ofemployees in their job functions, and the Product Stewardship Code involving health, safety, and environmental information, and employee education and product use feedback.
21 OSW 122402
WATER PCB-SD0000021382
W:Responsible Care
A Public Commitment
Product Stewardship Code of Management Practices
Purpose and Scope:
The purpose ofthe Product Stewardship Code ofManagement Practices is to make health, safety and environmental protection an integral part of designing, manufacturing, marketing, distributing, using, recycling and disposing ofour products. The Code provides guidance as well as a means to measure continuous improvement in the practice of product stewardship.
The scope ofthe Code covers all stages of a product's life. Successful implementation is a shared responsibility. Everyone involved with the product has responsibilities to address society's interest in a healthy environment and in products that can be used safely. All employers are responsible for providing a safe workplace, and all who use and handle products must follow safe and environmentally sound practices.
The Code recognizes that each company must exercise independent judgment and discretion to successfully apply the Code to its products, customers and business.
Relationship to Guiding Principles:
Implementation ofthe Code promotes achievement of several ofthe Responsible Care Guiding Principles:
To make health, safety and environmental considerations a priority in our planning for all existing and new products and processes;
To develop and produce chemicals that can be manufactured, transported, used and
disposed of safely;
~
To extend knowledge by conducting or supporting research on the health, safety and
environmental effects of our products, processes and waste materials;
-
To counsel customers on the safe use, transportation and disposal of chemical products;
To report promptly to officials, employees, customers and the public, information on chemical-related health or environmental hazards and to recommend protective measures;
22 L22403
WATER PCB-SD0000021383
To promote the principles and practices ofResponsible Care by sharing experiences and offering assistance to others who produce, handle, use, transport or dispose of chemicals.
Management Practices:
Each company shall have an ongoing product stewardship process that:
Management Leadership and Commitment:
1. LEADERSHIP: Demonstrates senior management leadership through written policy, active participation and communication.
2. ACCOUNTABILITY and PERFORMANCE MEASUREMENT: Establishes goals and responsibilities for implementing product stewardship throughout the organization. Measures performance against these goals.
3. RESOURCES: Commits resources necessary to implement and maintain product stewardship practices.
Information and Characterization:
4. HEALTH, SAFETY and ENVIRONMENTAL INFORMATION: Establishes and
maintains information on health, safety, and environmental hazards and reasonably
foreseeable exposures from new and existing products.
.
5. PRODUCT RISK CHARACTERIZATION: Characterizes new and existing products with respect to their risk using information'about health, safety, and environmental hazards and reasonably foreseeable exposures. Establishes a system that initiates re-evaluation.
Risk Management:
6. RISK-MANAGEMENT SYSTEM: Establishes a system to identify, document, and implement health, safety and environmental risk-management actions appropriate to the product risk.
7. PRODUCT and PROCESS DESIGN and IMPROVEMENT: Establishes and maintains a system that makes health, safety and environmental impacts--including the use of energy and natural resources--key considerations in designing, developing and improving products and processes.
23 OSH 122404
WATER PCB-SD0000021384
8. EMPLOYEE EDUCATION and PRODUCT USE FEEDBACK: Educates and trains employees, based on job function, on the proper handling, recycling, use, and disposal of products and known product uses. Implements a system that encourages employees to feed back information on new uses, identified misuses or adverse effects for use in product risk characterization.
9. CONTRACT MANUFACTURERS: Selects contract manufacturers who employ appropriate practices for health, safety and environmental protection for the operations under contract, or works with contract manufacturers to help them implement such practices. Provides information and guidance appropriate to the product and process risk to foster proper handling, use, recycling and disposal. Periodically reviews performance of contract manufacturers.
10. SUPPLIERS: Requires suppliers to provide appropriate health, safety and
environmental information and guidance on their products. Factors adherence to
sound health, safety, and environmental principles, such as those contained in
Responsible Care, into procurement decisions.
.
11. DISTRIBUTORS: Provides health, safety and environmental information to distributors. Commensurate with product risk, selects, works with and periodically reviews distributors to foster proper use, handling, recycling, disposal and transmittal of appropriate information to downstream users. When a company identifies improper practices involving a product, it will work with the distributor to improve those practices. If in the company's independent judgment, improvement is not evident, then the company should take further measures -- up to and including termination of the business relationship. This Management Practice should be implemented in conjunction with the Distribution Code of Management Practices.
12. CUSTOMERS AND OTHER DIRECT PRODUCT RECEIVERS: Provides health, safety and environmental information to direct product receivers. Commensurate with product risk, works with them to foster proper use, handling, recycling, disposal, and transmittal of appropriate information to downstream users. When a company identifies improper practices involving a product, it will work with the product receiver to improve those practices. If in the company's independent judgment, improvement is not evident, then the company should take further measures -- up to and including termination of product sale.
Relationship to Other Codes of Management Practices:
This code complements, and should be implemented in conjunction with, current and future Codes ofManagement Practices.
24 DSW 122405
WATER PCB-SD0000021385
T
Monsanto
DSW 117549
WATER PCB-SD0000021386
' Adams, L. - 1155 Allen, R. L. - 1580 Anderson, C. P. - 1560 Anderson, J. D. - F2WA Andrea, I. - 5090 Auxeafans, B. P - G3SA
Cahoon, C. - 1580 Camacho, L. - 5300 Campbell, W. J. - 02H Canaster, F. D. - 1880 Carpenter^ W.- D. - 03E Caruthers, R. R. - 1087
Easterday, P. A. - A3HL Edwards, D. B. -'G5NT'-> Edwards, R. J. - R3B Eley, B. W. - C2SB . Elias, J. - Medvy KentUK ; Ellis, J. - Edmntn.AlbCAK^
rL. Ceyanes, R.
1200
Baier, M. E. - 1820/00-7
Chamberlain, D.-BrlngtnOntCan
Balan, C. A. - 1500
Chan, S. - Hong Kong
Barnett, A. G. - C2SB
Chandra, Dr. U.-BrazilCBE
Barnett, J. W. - A3ND
Chavez, A. - 5300
'
Barrett, R. J. - 1260i
Cheever, R. L. - 1060
Beaver, E. R. - 1752
Choi, B. D. - 5280
Becker, R. P. - 1700
Clark, R. - Malvern PA
Begin, M. - CambrdgeOntCA Clarke, P. - I26QuV_ ^ '
Ellsworth, G. M. - 1775
Elmer, C. - A3NB
'
Eltz, R. W. - GG3K
English, H. B. - G5WA
Ereaut, G. A. - 5020 (5)
Erndle, J. F. - G5EA
ES&H Library - A3NH
Evans, T. F. - A3NA
.
Belle, R. J. - G5NL
Clayton, R. A.'ri.jjE2A-'
.
Farr, C. H/ - A2HE -$v' * t\. **
Benoit, J. P. - 5090
Clegg, G. Sr. tmSZ70V
' Farris, R.- H.. - T70
Berendt, R. T. - E2MF
'Colbert, W. Fwjrs 1700.-.
Fay, E. A. - 1290
Berger, R. - LaPorte, TXif- Collier, C. B. - 1690
Felder, J. D. - GAWE - : .
Bingham, J. B. - B2NA
' Collier, J. Rjj^. 1220 y;
Ferguson, J. J..'-vSOtfO
Bisbee, J. - 1880 .
.. Condray, J. R.-w- A3NA t:?{*i . Fields, R. L. - C2NF' : "'OS
Bishop, D. R. - G4WA. ' . Conner, P. R. -,>A3NB
* Fiorelli ,-A. C. - 1870 v `
Bishop, J. E. - 1900
Cook, C. W. - 5270
' Fissmer, R. J. - G5EA
Blackerby, D. - 1835
` Corbett, H. J. - DID
Fitzgerald, A. F. - ^G4EH
Blank, T. L. - 1740 '
" Corey, Jr. A. G. - 1775
Flynn, R. E. ~ 1729*
Blase, W. A. - G4EM
; Corley, T. L. - 1560
Folk, R. M. - EHL
:/
Blaylock, M. E. - B3NA
' Corser, M.,L. - 1260
Foppe", D. R.*:- EHL *
-
Board, W. J. - 1690
' Crone Jr., R. F. - 1690 '
.Ford, A. M. U4E . v
Boesch, L. J. - G5NV
Crowe, W.R. - 5010
... .. Foresma^i*; IT.: R. - GAWi?.^: '
Bohl, C. D. - A3NL
' Curtis, H. ;W. - CZNK
.Foart,
G4WD#^iT:
Boland, R. F. - 1760
Cushing, R. J. -. 1410 ' .
Bourget, R. L. - 1870
Boyd, P. M. - A2NG Boyen, V. E. - A2NB
Dahlen, R. G. - G4EM Dahlman,. I. - 1580
Boyle, W. J. Jr. - 1740
Dayton, F. H. - G5WA
Brackett, R. G. - 1825
`Debus, E. E. t C2SF
Brandon, R. A. - B3NA - DeFer, W.rrL. ^'}120Q-.i
Brasfield, E. N. - G5WA Braun, R. 0. - 5090
' Denner, D. K. - 1060 ' DePagter, J. G. - 1410
Brenner, H. R. - C2ND
Desroches, R. - 5090
Franchetti^!-' V. M. - 1870 . Freeman, X. - T060 T \
'.r.^French, ArJX.^ '1729. v;; . ::
Frie'dlandehf, B.*R. &3NA * " Fuhj~emann, T. WV C2SE - .
Fukiichi, R. 'M. .- 1525 : ' v. Fuller, yG.v.. - C2SC/ , . Funke; R. - Mansfield,OH
* /. ' Gaetan, J. - WoodstckOntCAK .
Bresovec, P. - 1050 Bright, J. O. - F4WA
, DeVet, G. - 1580 r4`
.
'Dieterich, D. C. - 1150
...Gaffey, W. R... -'A3HK;.:f ' Galloway, J. - Glen.-;ELu'rne MD
Brodsky, P. H. - 02A Brooks, J. J. - BB2E
DiGiovanni, M. P. - 1090 Di Luca, P. - 1410
Ganatra, B. - 1585 -`.:V .
Gaul, J. M. - 1560
p >'.
Brouwers, J. - 5035 Brown, J. L. - 1060 Brown, R. L. - 1850 Bryant, F. J. - 1200 Bucknell, R. W. - 02A Burch, J. F. - 1440 Burns, M. D. - B3SB
Dixon, W. D. - 03C Dowdy, S. E. - C3NK Downes, J. E. - G4WR Driscoll, H. B. - G4NA Dubleman, S. - BB5F Duesenberg, R. W. - DIP Dushney, J. P... - 1410
Geddes, R. - 1850 Gibbs, M. E. - R4B Gilhousen, B. J. E2NK Gledhill, W. E. - U4G Graham, R. W.-Sweetwater Grattan, E. P. - A3SA Gray, M. B. - 1200
Butler, D.-Paramount, CA Buzbee, T. D. - 1580
Dutra, G. A. - 03F
Griffin, G. H. - G4EK Grigg, R. G. - 1850
_
Guarraia,_L. J. - 03G
LIST 304
OSH 117550
WATER PCB-SD0000021387
Guerra, J. - Toluca HEX Guilliams, R. E. - 1200
Jos1in, R. H. - G4VS Jurevic, E. J. - C2NJ
Hachey, G. A. - A3NL Hacker, S. N. - 1690 Haechrel, P. - 1740 Hagood, J. A. - 1200 Hammond, B. G. - B2SC Harbison, E. H. - D1T Harness, R. L. - C2SB Hart, J. F. - 1418 Hartlen, E. D. - 1087 Harvey, T. - B2SC ` Hathaway, C. E. - R3B Hauser, G. L.-RchsterKeat Hawk, E. J. - B2NA Healy, C. E. - A3ND Hebert, L. F. - 1670 Heininger, S. A. - DIR Helms, L. T. - 1160 Helscher, T. M. - 1920 Hendrikse, E. E. -G4NC Henshaw, J. L. - A3NL Herron, E. - GonzlaLA Higley, L. W. - E1NH Hill, B. J. - G4WR Hiller, F. I. - 1080 Hirsch, J. C. - 5000 Hoard, R. S. - E2NA Hoegel, D. C. - 1290 Hoogheem, T. J- - C2SD Huff, H. R. - G5WA Hume, J- C. - B3NA Hundley, C. - 1900 Hunt, P. E. - A3NB Hunt, W. M. - F3WA Hunter III, J. C. - G5NG Hwang, Y. C. 5280 Hyland, J. P. - G4WT
Ingenthron, G. D. - C2SB Irwin, G. H. - B3NA Iversen, T. G. t G5HV
Jackson, J. B. - 5040 . Jamro, E. S. - 1290 Janssen, E. P. - F2EA Jansson, R. E. - G3NE Jaworski, E. G. - AA4A Jeannot, P. M. - 1825 Jenkins, R. D. - 1250 Jervis, J. D. - 1690 Johaansen, F. R. - A3ND Jones, R. N. - G5WA Jones, W. H. - 1700
Kaimin, J. J. - 1250 Kayahara, Y. - 5265 Kearney, F. E. - G4WT Keffer, C. W. - C2SB Keigler, W. - GlnBumeMD Keliher, J. F. - G5HV Kennar, G. A. - 1870 Kennedy, K. H. - 1760 Kerr, J.-Rchestr,KentENG Kilby - J. L. - B3NA Kilkenny, J. E. - G5EK King, T. M. - 04C Klieve, J. R. - C2SB Knight, J. E. - 1260 Knoop, H. E. - 1918 Kocurkovic, J. V. - F1WG Koenst, J. W. - 1752 Koh, N. T. - Singapore Kraemer, C. B.-LeicesterUK Kramer, R. M. - 03A Krawczyk, D. S. - 1700 Kronenber, J. M. - C2SK Kucera, R. J. - 1260 (3) Kulig, M. A. - 1870 Kunes, W. R. - G5WB
Labanosky, J. A. - 1080 Lafferre, T- H. - G4NU Lamkin, R.E.L. - G4NA Landholt, W. - 1087 Lange, V. - 03A Lane, J. H. - 1020 Lange, V. J. - 03A Lannert, K. P. - 04C LaPlante, G. L. - 5090 Larsen, C. J. - 5040 (50 No Covers) Lawton, R. P. Jr. - G5EB Lawyer, R. E. - 1260 Leach, J. - 1835 Ledgely, L. J.-WdstckOntCAN Lemos, G. A. - 1870 Lepriol, R. - Vichy, FRA Levinskas, G. J. - A3NB Lewington, C. -SidneyAUS Light, D. M. - 1670 Liademann, Jr. R. E. - C2NJ Lingam, S. K. - 5295 Littlejohn, S. E. - B2ND Logie, I. -LeicesterUK Longfield, S. J. - 1720
Lougin, P. - 5040 (2) Lott, K. V. - 1850 Love, J. R. ~ A2SJ
Hackie, E. J. - G5WA
MacMillan, K. A. - 5080
Madden, J. G. - 1410
Magin, R. W. - 03C
Mahler, M. E. - 1670
Mahoney, R. J. - D1V
Malfitano, D. M. - 1720
Malik, J. M. - BB5F
Malloch, C. D. - A3NA
Maniscalco, R.-BrlngtnNJ
Marchi, E. L. - 5000
Marquez, R. - 1200
Marschall, M. V. - 1870
Martin, F. -CemayFR
Mason, R. J. - G4N0
Matteucci, V. T. - G5NR
Matthews, F. B. - 1760
Matyus, D. M. - 1850
Matzner, E. A. - G5NV
Mauldin, G.-A. - 1087
McCarville, W. J. - A3NA
McComb.C. H. - 1090
McCombs, M. W. - 1740
McCullough, C. M. - 1850
McCune, L. C. - 1010
McDannold, J. E B2SB
McGavock, M. - 1760
McGrath, A. M. - B3SA
McGuire, J. N. - G4WM
McIntyre, E. - 1410
McKee, G. L. - G4NC
McKenna, L. W. - G4NL
McMakin, J. E. - 1290
Meitner, P. R. - F1WE
Mertens, M. - 1683
Michalski, B. A. - 1793
Mickelson, D. D. - C2NA
Mieure, J. P. " G4WR
Miles, J. A. - B2ND
.
'
l
v ?-
Miles, M. G. - C1ND Miller, K. S. - 1670 Miller, L. A. - B2SA Miller, M. E. - G5NA Minarich, D. - 1815 Molloy, J. W. - G4NJ Montague, M. J. " BB3B Moore, E. L. - F2WB Morgan, F. W. - BB2E Morganthaler, W. H.-04B Muhs, J- H. - 1010
-
LIST 304
DSW 11755J.
WATER PCB-SD0000021388
IT
Mullias, M. L. - 1920 Mullis, J. 0. - 1690 Munier, J. C. - VichyFR Murphy, M. J. - A3NX Murphy, R. J. - 1740 Murrell, C. R. - 1155 Musch, D. D. - 1918
Nair, R. S. - A3ND
.
Navarrette, C. F. - 5050
Nelson, K. N. - 1580
Nisbet, J. H. - 5050.
Norlander, C. D. - G5NV
Nurenberg, D.-1820/0011-6
Occupational Medicine Director - A3NB
Ochsner, J. - 1540 O'Connor, G. E. - F1WF Oliver, T. B. - 1585 Osborne, - G. A. - 1410
Paget, E. - 1820/007-1 Panasiewicz, R. P. - 1500 Paradis, L. P. - G4WS Parthasarthi, M - Bombay Patel, M, N. - 1418 Paton, C. - 5510 Paul, R. - Posen, IX Peirce, M. - 1900 Perdue, W. S. - 1220 Perica, K. M. - 1290 Petersen, D. X. - 1683 Peterson, G. X. - 1650 Pflederer, R. X. - 5210 Pier, R. G. - G5NX Pierle, M. A. - G4WT Plant hanager - 5330 Plecia, F.' H. - C2SB Plotnick, M. - 5090 Politte, A. J. - 1720 Potter, R. G. - G4NH Price, D. B. - G5NG _ Pridham, G.-ZEKSMalvrnPA Privott, W. J. - B2SA Proctor, S. I. - F2WK
Quick, A. J. - 1815
Rademaker, J. C. - 1050 Ransaw, I. - 1560 Rapko, J. N. - G5NS Rathmer, E. - AhausFRG Ratts, K. W. - 03C Reding, N. X. - C2NA
Redington, D. B. - A3NA Redmond, T. B. Jr. - 1775 Reiners, S. D. - F3WA Reining, F. E. - G4N0 Reynard, F. - AA3A Reynolds, R. W. - C3NA Rhoades, R. E. - 1630 Rhodes, V. X. - G4WR Rhyne, R. H. - 1260 Richey, W. S. - 1220 Riek, R. F. - 1010 Rivers, A. S. - F2EA Roarty, J. P. - 1290 Robinson, E. C. - A3ND Robinson, S. J. - G5NA Rodriquez, F. - Madrid . Rogers Jr., C.J. - 1440 Rogers, P. E. - 03C Rohr, J. F. - 1150 Rose, R. X. - XansngMI Roth, C. R. - A3SD Rozelle, G. D. - 1080 Rusczek, R. A. - 1870 Rutledge, X. R. - 1793 Ryan, J. P. - G5NX
Sabet, A. S. - 1010 Saito, S. - Tokyo JPN Sandberg, J. M. - 1670 Sandfort, R, M. - 5425 Sarvono, B. - 5325 Saunders, X.V.J. - B3SF Schafbuch, J. S.- A2SF Schannon, M. X. - B2ND Schelcher, P. -CemayFRANCE Schneiderman, H. A. - DlV Schroeder, A. R. - 1900 Schroeder, M. - 1740 Schultz, R. G. - 04B Scott, M. A. - 1700 Scott, R. M. - A2SK Sellew, R. F. - G5NV Senger, J. H. - A3NA Serdy, F. S. - C2SC Shayer, X. D. - F4EA Shelton, P. E. - 1630 Sherman, Jr. H. C. - 1670 Shimada, K. - 5270 Short, R. D. - A3ND Silva, E. - 1200 Sliney, D. X. - G4NJ Slocum, T. J. - B2ND Slowikowski, W. H. - G4NA Smid, M. J. - F2EC Smith, C. A. - 1793
XIST 304
-3-
Smith, P. - E2NK Smith, S. D. - 1740 Solley, X. W. - 1580 Son, M. - Incheon, Korea Spies, G. J. - A3NX Spiller, R. W. - G5NA S&PP - A2NB Starr, M. S. - 1870 Stegen, D. W. - G4NA Stevens, M. W. - A3NG Stocker, D. C. - G5NG Stohr, R. A. - G5WB Storms, K. E. - A3NX Stout, X. D. - EHX Street, R. W. - C2SC Stroble, F. A. - DIF Stroup, M. A. - G4N0 Suba, X. A. - C2SE Suk, D. - Columbia, SC Sumner, W. - 1580 Sweerman, J. - Cernay, FR Sweets, C. A. - F4EA
Tatum, V. W.-- 1585 Tennison, S. - 5295 Thake, D. - EHX Thorne, J. G. - 1729 Thurman, C. H. - G5NT Tolloczko, A.W. - 5000 Tominack, R. X. - A3NB Toy, H. D. - 1900 Tuk, A. C. - 1670 Tuley, J. X. - G5EA
Uelner, A. F. - A3NF Uible, Jr., F. R. - F2EN Uihlein, Jr., J. J. - G5EC Unland, M: X. - 04B
Vaca, A. - 5300 Vanderstall, H. - 1683 Varnado, W. W. - G5WM Verfaillie, H. A. - C3SJVermeire, J. - 5280 Vezzetti, D. M. - 1720
Waldbeser, J. H. - F2WJ
Wallen, N. - 1835
Walter, R. X. - A2SC
Warborg, T. E. - 1020
Ward, D. P. - C2SK
Ward, P. K. -
1690'
Ward, T. J. - 1630
Ward, W.--C. - 1630
Wasson, R. X. - 04B
OSW 117552
'!
WATER PCB-SD0000021389
Watson, K. - MedwyKentUK Weaver, G. K. - 1440 Weingartner, C. F. - G5EC
Weishaar, M. F. - G5WM Welch, H. - Exac Welter, J. P. - F3WG
Wesley, G. J. - C2SB
Wildsmith, G. - G5WB
Wiley, J. G. - 1690
.
Wilkens, M. P. - C3SE
Wilkinson, W. A. - R2B
Williams, A. E. - 5425.
Williams, D. E. - F2EK .
Williams, G. - Fisher
Williams, H. L. - G4NL
Williams, L. S.-1825/A1E
Wilson, T. -BurlngtnOntCAN Wind, D. R. - 1850
Winkelmann, J. R. - 1760
Withers, W. W. - C2SA Wojick, R. B. - 1870 .
Wollenberger, J. B. - E1NG
Wong, C. T.-Pasir Gudang Woods, t. - 1250 Woods, R. L. - 1580
# *
Yanne, E. - 1870 Young, D. A. - MelbourneAUS Young, G. A. - G4WF
Zalba, J. - 5000 Zendejas, R. -TolucaHEX Ziemann, T. E. - C3ND Zurlinden, Jr., P. R. - 1010
LIST 304
DSW 117553
WATER PCB-SD0000021390
.>-L. H-J. Corbett, D-l-D
Hay 22, 1989
Worldwide Environmental Guidelines
Distribution List
Following the practice of the past several years, Monsanto's six worldwide environmental guidelines have once again been revised and updated.
These guidelines have been approved by the Corporate Environmental, Safety and Health Committee and represent our "rules of the road" for environmental, safety and health programs across the corporation. While requirements vary across different units of the corporation and worldwide guidelines require some compromise to permit application to all operating units, compliance with the spirit of the guidelines is not optional. Modifications which achieve the spirit of the guideline and are more appropriate to a local condition are permitted, but not in any case where the level of protection, quality assurance or safety is less than the intent of the guideline.
As an additional aid to performance in environmental, safety and health issues -- we are including an environmental, safety and health vision for the corporation. This vision statement together with premises and indicators has been widely reviewed by operating units within and outside the U.S. It represents a vision of the company we would like to become and should be working toward. Actions taken by all employees of Monsanto should be consistent with the tone and direction of this vision. Further, where current performance does not measure up to the longer term expectations as described in the vision, the heed for more aggressive improvement plans should be self-evident.
This vision statement is intended to complement the worldwide guidelines as we proceed toward achieving "great company" status in environmental, safety and health performance.
While elements of the vision and guidelines may be discussed with individuals outside the company as appropriate -- copies of the guidelines should be considered "company confidential".
attachment
OSW 117554
WATER_PCB-SD0000021391
MONSANTO'S VISION ENVIRONMENTAL, SAFETY AND HEALTH PERSPECTIVE
A company which develops and markets only products which benefit society without unaccept able risks to any group.
A company where major environmental, safety, or health incidents do not occur.
A company with recognized and demonstrated concern for our neighbors, our employees, and both local and worldwide environments.
A company which is viewed by its publics, regula tory agencies, and stakeholders as responsible, ' open, and honest -- a constructive component of society and the communities in which we do business.
A company which encourages outside peer review of its decision making processes and proposed actions in environmental, safety and health matters.
A company which as a matter of policy, separates the issue of the "right thing to do" from the issue of cost or affordability.
A ccjpany which monitors employee health on a continuing basis and investigates possible health issues affecting current and former employees.
A company which knows first whether its products, processes, plants, or people may be causing potential problems.
A company which maintains a continuing multi media toxic waste minimization program empha sizing source reduction and recycle with an ultimate goal of achieving a de minimis emissions level.
A company which achieves its ESH objectives at capital and operating costs which do not signifi cantly impair growth and profitability.
OSH 1J.7555
WATER PCB-SD0000021392
2- -
A company which turns its exemplary practices into a competitive advantage.
PREMISES
We will organize to achieve maximum effective results.at the lowest cost.
We will organize to assign primary execution responsibility to operating entities.
We will organize to provide analysis, interpret ation, strategic planning, oversight and quality assurance by groups which are independent of short term profit considerations.
We will organize to provide state of the art
scientific capability to ensure ESH results
without the need for each entity to maintain
fully proficient and complete professional skill
bases.
-
We will take a leadership role in a variety of industry and academic initiatives to influence public opinion, stay abreast of trends, and achieve our goal.of public approval. This includes active participation with environmental groups, trade associations, professional groups and academic institutions which have goals compatible with Monsanto's objectives.
PREDICTORS AND INDICATORS OF SUCCESS IN ACHIEVING OPR VISION
As a minimum, full compliance with all laws, regulations, and permits on a worldwide basis.
Continuing reduction in injuries to employees and reduction of unexpected incidents and spills.
Continuing reduction of overall waste production with emphasis on toxic and hazardous air emissions. Waste minimization at the source is preferred over waste treatment.
Rapid approval of new products, at least equal to the best in our industry.
Participation in the public debate on ESH issues
via active membership in relevant organizations,
trade associations, environmental groups, -
professional associations, etc. *.
*
DSW 117556
WATER_PCB-SD0000021393
-3Positive employee and community acceptance of our performance. Maintenance of strong relationships with Federal, State, and Regional institutions, in all countries in which we operate or do business. Maintenance of management skill and knowledge bases to achieve most effective legislation and regulations, interpretation and implementation of regulations. Maintenance of professional skill bases in toxicology, occupational medicine, epidemiology, industrial hygiene, safety and property protect ion, quality assurance, analytical capability, risk assessment, and others as required by future events. Rigid multi-discipline .quality assurance review of new products, new processes, existing pro cesses, products and facilities.
DSW 117557
WATER_PCB-SD0000021394
MIn. WORLDWIDE GUIDELINE
EFFLUENT AND EMISSION CONTROL
Reduce pollutants in effluents and emissions from Monsanto operations to meet corporate targets, going beyond those levels either required for regulatory compliance or necessary to protect health and the environment.
PROGRAM
EFFLUENT CONTROL: Control options for both direct
and indirect (i.e., to Publicly Owned Treatment Works -
POTW) liquid discharges from Monsanto operations will
be developed consistent with compliance dates in permits or
other enforceable instruments aiyj. to meet internal Monsanto
needs. Substances subject to such controls will include those
listed pursuant to Section 307(a) of the U.S. Clean Water
Act, those substances known to be present in proposed or
promulgated effluent limitation guidelines, or.other site-
specific pollutants identified by the. plant which appear to
warrant consideration, including those reported via SARA
Tide m. Section 313. For ex-U.S, locations, use a site-
specific list which is equivalent to flie.U.S.-EPA lists.
r '!
.
For each location where any of these substances are used or
produced, address the following: .
1. Regulatory compliance -- Develop specific information necessary to identify control options to ensure compliance with regulatory-driven limitations in permits or other enforceable instruments. Such information should include substance quantification profiles at .reasonable levels of confidence and could include factors such as variations due to seasonal effects, product mix, hydraulic loading, production capacity, waste treatment variables, or other site-specific parameters. Timetables for this effort should be developed on a site-specific basis, consistent with needs to meet legally enforceable compliance.
2. SARA Section 313 substances.^ Conduct a site-
specific substance-by-substance review of significantly
reported SARA Section 313 releases (for both direct and
indirect discharges) for those substances not addressed by
limitations in permits or other enforceable instruments. '
Within the framework of the corporate waste minimization
program, reduce the quantities ot suen releases.
'
3. Water quality -- Conduct an aquatic safety assessment to determine the measurable impacts, if any, of Monsanto's effluents on receptor water quality. This should cover both direct and indirect discharges (if appropriate), with the latter impacts based on POTW effluent, where pos sible, including judging Monsanto's contribution to
MONSANTO COMPANY
the POTW's effluent. Details for this assessment and appropriate response actions should be developed based on individual site-specific needs.
Operating units will annually review, and adjust as neces sary, the priorities and timetables for the above programs.
EMISSION CONTROL: Monsanto intends, by the end of 1992, to reduce air emissions, worldwide, by 90% for the chemicals reported on the SARA Section 313 reports for 1987. Beyond 1992, Monsanto will work toward an ultimate goal of zero emissions for these same chemicals. The baseline in the U.S. for this reduction will be the chemicals and quanti ties on the 1987 SARA Section 313 emissions report, with comparable programs being developed for the ex-U.S. opera tions. Operating units will establish and implement plans to achieve these reductions and will issue annual progress reports.
Conduct an assessment of potential human health impacts for selected routinely emined air pollutants and develop appropriate control strategies to reduce identified potential unreasonable risk of harm to human health in surrounding communities. In addition to providing additional under standing of the potential human health impact from Monsanto plant operations, this information .will facilitate Monsanto responses to regulatory proposals and future permit needs.
The list of air pollutants to be studied include: (a) those listed and regulated under Section 112 of the U.S. Clean Air Act; (b) those currently being reviewed as candidates for listing by EPA as Section 112 pollutants; (c) those for which EPA has established cancer unit risk values; (d) those con tained on the International Agency for Research on Cancer (IARQ groups 1 and 2A lists; and (e) other site-specific pollutants identified by the plant which appear to warrant consideration (including those in significant quantities reportable via SARA Section 313>_ For ex-U.S. locations, use any local regulatory lists which are equivalent to the U.S. EPA lists.
Each Monsanto location will cany out the following program: ^
OSW 117558
SECTION 1
WATER PCB-SD0000021395
EFFLUENT AND EMISSION CONTROL (continued)
1. Identify, for each air pollutant selected for review, all emission point sources (ongoing, continuous, and intermittent), as well as area and volume sources where the substances are released into the atmosphere.
2. Estimate for the selected air pollutants, their emission rates from each source.
3. Rank each of the selected air pollutants to determine their relative priorities for further evaluation using a chemical prioritization protocol established by the Monsanto Air Steering Committee which utilizes workplace exposure guides and estimated emission rates.
4. Develop work plans to complete the detailed assessment of priority 1 and major 2 pollutants by 7/1/89 (by date consistent with local needs for ex-U.S. locations). For remaining prioritized pollutants, work plans and further evaluation will be conducted within the confines of. existing resources.
5. Estimate the potential maximum downwind concentra tion for each pollutant at receptors representative of the exposed population, utilizing appropriate dispersion modeling techniques incorporating refined quantification of emissions based upon relative priorities (i.e., ranging from point source measurements for priority 1 to best estimates for priority 4).
6. Assess the potential for human health impacts at com munity receptor points using the results of the dispersion analysis, and determine if there is, or is not, a potential for unreasonable risk of harm to human health.
7. Define appropriate, cost effective controls to reduce risks to acceptable levels where a potential human health concern exists and take actions to implement such reductions.
For U.S. locations, complete the fust six steps above for priority 1 and major priority 2 pollutants by 7/1/89, complete step seven on a timetable consistent with local needs, and for the remaining prioritized pollutants by a date consistent with resource availabilities. For all ex-U.S. locations, complete the seven steps for all priorities by dates consistent with local needs.
GENERAL: The following program elements will be imple mented as required.
1. Sample the significant emission and effluent release points of each new or modified process after startup to confirm that no pollutant, in an amount having potential to endanger health or the environment, exceeds those
- levels specified by the design and/or contained within any applicable permits.
2. Operating Companies will periodically report data on permit exceedances and reportable releases (including those reportable under CERCLA), with performance to be reviewed annually. During 1989, develop uniform corporate reporting criteria and obtain ESH Committee approval.
(Revised and Approved by Environmental, Safety & Health Committee April 25, 1989.)
SECTION 1 Page 2
DSW 11755.9
WATER_PCB-SD0000021396
MIru
i
WORLDWIDE GUIDELINE #2
WASTE MANAGEMENT
Design and operate facilities to minimize in waste streams the routine and accidental release of pollutants to
the environment. Over the long term, work toward the ultimate goal of zero releases to ail media. For
wastes that remain, use waste disposal practices that achieve compliance with regulations and which achieve
acceptable environmental impact, no health effects, minimum long-term liability and cost effectiveness.
Continue waste management programs that establish Monsanto control of disposal and that favor alternatives
to land disposal.
.
PROGRAM
Except as modified by item S. below, this guideline applies to all worldwide Monsanto facilities.
. ... T\
' -
. -:'j
1. Release Reduction
a) Routine Releases
Each operating unit will establish a program which targets multi-media reduction of releases in waste streams to the environment, establish ing numerical reduction goals. Units will report progress annually.
In the selection of alternatives for pollutant release reduction from processes, the following order of preference will be used:
Reduction of source generation through process design and modification.
Reuse, recycle or co-product sale.
Incineration or other treatment to reduce the volume or toxicity of pollutant streams.
Responsible disposal of treatment residuals or wastes not amenable to the above.
The operating unit programs will integrate into release reduction plans a corporate goal to achieve a 90% reduction, worldwide, of 1987 SARA Section 313 reported air emissions by the end of 1992.
Releases to air, water or the land which continue in spite of reductions will be assessed as applicable through the programs outlined in Guideline # 1 and in #2 (below) to assure no danger to health and the environment.
'Ai listed m 40 CFR 261.33(c). plus anjr mixtures containing greater than 5%.
Wastes with heat of combustion of greater than 6.000 BTU/#.
MONSANTO COMPANY
b) Accidental Releases
Accidental releases that are reportable to regulatory or response agencies, or that involve evacuation, significant community response or media coverage, will also be reported internally together with an action plan to prevent recurrence. The operating units will establish programs as necessary to eliminate such occurrences, working toward a goal of zero events. Progress against this goal will be repotted annually through the Manufacturing Management Council to the ESH Committee.
c) WasteDatgbases
Operating units will develop and utilize multi media databases on releases to the environment to enable repotting against operating unit goals and against the 90% SARA Section 313 air emission reduction target. A waste-stream based U.S. database will also be maintained to facilitate external reporting and as another internal measure of release reduction progress.
2. Waste Management
'
Landfill of "acutely hazardous" wastes' and "incinerables", will not be practiced. Fixation of particularly mobile, persistent or bio-accumulative wastes will be accomplished wherever warranted and feasible, or where required by regulations.
Land disposed wastes which are not subjected to management as "hazardous" waste will be evaluated for present and future environmental risk and managed
_
OSW 1L75A0
SECTION 2 ^
.
Page 1
~
WATER PCB-SD0000021397
2. Waste Management tcontinued)
in an appropriate manner which has been reviewed by the unit Director of Environmental Operations. (To be completed by 12/31/90.)
Waste contractors will be subject to contracting and assessment requirements (See Guideline #3). The number of off-site hazardous waste incinerators used will be minimized. In the U.S., off-site Class 1 . . landfills used will be approved by the ESH Committee and limited in number.
Medical wastes generated at Monsanto locations will be disposed of via incineration. Assurance of destruction will be obtained via manifest, or other equivalent approaches if manifest is not available. ' (For the purposes of Guideline #5, outside processors used will be considered Secondary Services.)
An evergreen record of both on-site and commercial waste treatment, storage and disposal sites will be maintained by each plant.
Monsanto will retain ownership of all property known to contain wastes with the potential to cause injury to health or the environment unless otherwise approved by the ESH committeqjfhe use of company facilities to treat, store or dispose of non-Monsanto wastes is normally discouraged. Any such use or joint ventures for waste manage ment must be reviewed and approved by the. ' ESH Committee.
3. Deepwell Injection Program
Monsanto will continue to operate its deepwell disposal systems in a sound manner protective of public health and the environment. Each plant using on-site or off-site deepwell disposal will have and maintain contingency plans for exiting deepwells. There will be no new use of deepwells except as approved by the ESH Committee on an exception basis. All new project appropriation requests will be based on the economics of disposal technology other than deepwells.
4. Corrective and Remedial Action
When on-site abandoned waste or groundwater contamination is discovered, appropriate assessment and corrective action will be carried out. Any ' necessary projects will be scheduled to expedite remediation in a planned, orderly process.
When we become aware of possible involvement in "Superfund" sites, we will actively participate in generator group efforts to achieve settlement and
expedite cleanup. At sites where we are a/the major contributor, we will seek a leadership role when appropriate to facilitate resolution. The operating units will cooperate to establish responsibility for sites where several units contributed wastes. A goal of the corporation is to resolve as soon as reasonably possible our liability and remedial plans for sites where we have major responsibility.
We intend a lessened legalistic approach to site cleanup negotiations. Where our responsibility is fairly established, we will not delay cleanup unnecessarily by legal, yet negatively perceived litigious steps. We will pursue fair legislation and regulations on the general issues in the public arena, but minimizing legal risk will not be the determining factor in site-specific decisions.
3) Ex-U.S. locations
The above program elements and timing will be implemented at ex-U.S. locations, but with modi fications as necessary to reflect local limitations, restraints to compliance, and the extent of Monsanto's operating control. Status and direction of local programs will be reviewed in planned environmental audits of these facilities.
%
0
(Revised and Approved by Environmental, Safety & Health Committee April 25, 1989.)
i)SW 1J.7561
SECTION 2 Pace 2
WATER PCB-SD0000021398
1 1 1991
Monsanto
FROM (NAME, LOCATION, PHONE)
N. L. Reding DIR 4-2106
DATE: SUBJECT: REFERENCE: TO:
May 30, 1991
cc: Env. Policy Committee
Deep Wells
!)
(
ES&H Guidelines Manual Holders
#
r'-" " '
Please place the attached, revised deep well policy statement in your manuals as an adjunct to Worldwide Guideline 92, The Guideline itself will be revised in the future to incorporate this initiative.
The revised policy reflects the deliberations of the Environmental Policy Committee and the Advisory Councils of MCC and MAC, and will guide the ' corporation's programs through the year 2000. It is supplementary to current operating unit waste elimination goals and, when implemented, will signifi cantly improve the corporation's progress toward reaching the goal of zero effect on the environment.
Every individual affected by this policy can help the attainment of this goal by focusing technology on reducing the creation of these wastes and converting such actions into a competitive advantage for their business.
NLR/jm/AOlMEMO.NLR Attachment
sw 117562
WATER_PCB-SD0000021399
APPROVED DEEPWELL POLICY
June 1, 1991
STATEMENT
`
Project programs within the operating units will be coordinated to discontinue, by the end of 1999, the deepwell injection of waste streams except for dean brines or treated wastewaters which are best managed environmentally in deep injection wells.
By the end of 1995, the optimal technical strategy(ies) for total withdrawal from wells will be selected as a contingency for possible earlier mandatory action. At Luling, only, this action indudes an ARDT estimate to achieve non-brine, treated surface discharge. Before 1995 and thereafter, the operating units will continue where possible to challenge the technical impediments to total withdrawal, based on surface discharge of nori-brine treated wastewater.
New or expanded internal or external uses of deepwells are discouraged and will be considered by the EPC only on an exception basis and within the constraints of this policy; the economics of any project appropriation request for such use must be based on disposal technology other than deepwells.
OBJECTIVES
1. Substantially reduce SARA reported releases to deepwells by 87% by the end of 1995.
2. Achieve 70% reduction of Priority 1 pollutants (organics and toxic inorganics) to wells via Waste Himination/Waste Minimization efforts, by the end of 1995.
3. Substantially eliminate SARA and Priority 1 releases to deepwells by the end of 1999.
4. Achieve surface discharge of treated effluent at Chocolate Bayou. At Luling, provide that only dean brine is injected, brine that is otherwise .treated to meet Effluent Guidelines (CWA). At Pensacola, achieve treated effluent wastewater suitable for discharge under Effluent Guidelines but plan to continue injection due to regulatory issues.
OSW 117563
WATER_PC B-SD0000021400
INDICATORS
The following indicators are identified for tracking of progress:
Completion of targeted projects.
End-of-1995 and end'-of-1999 releases of SARA chemicals and Priority 1 substances to injection wells.
t
1995 completion of contingency project definition.
ahd3
Approved by EPC Committee, 4/16/91
DSW 117564
WATER_PCB-SD0000021401
PROJECT TIMETABLES
Chocolate Bayou
Project
Spent Acid Recovery (SAR servicing AN, MHBA, NTA. Includes limited in battery wastewater ' treatment for DSIDA
New Biotreatment unit and Sludge Handling Facility.
. TOTALS
YEAR On-Line
1995
1999
Capital SM
75(1)
Operating Expense,SM
8
30 105
7 ~15
idditio^trSAR^1^1 fr miscellaneous Waste Elimination projects in
Pensacola Project
Liquid Waste Incinerator for concentrated organics, including HMD Ion Exchange
Year On-Line
1995
Capital ____SM____
10-25(1)
Operating Expense.$M
2-6(1)
3-Staqe Biotreatment including Sludge Disposal and Teritiary Filter. Also provide Spare ODW Evaporator for KA and Copper Ion Exchange for Adipic.
1999
37-22
9-5
TOTALS
47 11
(l)Larger values assume some biological treatment installed early to achieve 1995 Waste Elimination goal.
Lulinq
Project
Catalytic Chemical Oxidation Process for essentially complete organic removal, GI Wastewater. Achieve clean brine.
Organic Removal and Ammonia stripping of ACL/CYA Wastewater. Achieve clean brine.
Year On-Line
1995
1995
Capital SM 35
8
Operating Expense,SM
13
2
OSw 117565
TOTALS TOTALS. ALL PLANTS
43 195
15 41
WATER_PCB-SD0000021402
PRn.TECTinN OF RELEASE REDUCTION
w*<;re Elimination/Waste Minimization Proarams, Prioritv 1 Release to Iniection Wells:
Base Year 1987
Actual 1989-
Projected End-of-1995
Projected End-of-1999
Lulino MCC & MAC Programs
`
4.0
17.3
2.6
Nil
Pensacola
70.7
86.7
37-201 .
4.3
Chocolate Bavou MCC fit MAC Programs
47.8
59.8
9.7
None
TOTALS %Red'n vs. 1987
122.5
163.8
49.3-32.3l 60-74Z
4.3 96Z
xLower value assumes some biological treatment installed early to achieve 1995 Waste Elimination goal.
SARA 313 RELEASES TO DEEPWELLS. M LBS
Plant Luling Pensacola
Chemical
All
NH NO, Otner
Choc. Bayou
NH S04 Otner
TOTAL SARA 313 % RED * N VS. 1987*
1987
15
22
-
. 22
171 8
179
216
1989
4
23 1
24
196 6
. 202
230
Projected End '95
0.4
4 0.5 4.5
20 4
24
29
87%
Projected End '99
Nil
Nil Nil
0 0 0
Nil
"100%
DSW 117566
WATER PCB-SD0000021403
fUl
InJ
WORLDWIDE GUIDELINE
#3
PLANT ENVIRONMENTAL ASSESSMENTS
A program of environmental assessments and audits of all plant sites will be maintained in order to assure regulatory compliance and the protection of the surrounding environment.
PROGRAM
1. Environmental assessment documents (information such as local air and water quality, relationships with regulatory agencies, and the effects of our presence on the surrounding environment) will be prepared for each operating location. Documentation of subsequent changes or additions to assessment contents will be filed with assessments at die plant site so that an update can readily be prepared should the need arise. Executive summary sections reflecting .
.. long-range plans and highlighting key environmental issues will be updated annually and transmitted as information to Environmental Managers.
2. Compliance audits for large and environmentally sensitive sites will be conducted on a three-year maximum cycle with other sites to be audited at least every five years. Audit follow-up plans will be reviewed semi-annually.
3. Groundwater assessments will be maintained for all major locations and for lesser sites with known groundwater issues. The assessment status and plans will be updated in the second quarter of each year.
4. Each location shall maintain a groundwater protection plan to include inspection, testing and maintenance of facilities with the potential of contaminating groundwater (i.e., sewers, process lines, sumps, tanks, loading/unloading areas, etc.). The ground water protection plans and designs shall be commen surate with the risk posed by the specific situation.
5. New, replacement or expansion facility designs (including sewers and lines) should consider aboveground and/or double containment, improved materials of construction and/or cathodic protection to provide improved assurance against groundwater contamination. New, replacement or expanded surface impoundments for wastewater treatment or storage will be approved by the ESH Committee on an exception basis.
6. . New storage tanks for materials that could potentially cause contamination will be provided with impervious secondary containment (dikes, liners, vaults, double wall, etc.) unless a clear showing is made on a tank-by-tank basis during project reviews that vessel contents (e.g. dilute wastewaters) or setting (e.g. in-battery containment, other adequate containment systems) do not warrant such containment. Existing storage tanks will be addressed and reviewed through normal environmental audits.
(Revised and Approved by Environmental, Safety and Health Committee April 25, 1989.)
MONSANTO COMPANY
'
DSW 11756.7
if
SECTION 3 Pace 1
WATER PCB-SD0000021404
WORLDWIDE GUIDELINE
#4
EMPLOYEE AND COMMUNITY SAFETY AND HEALTH
Monsanto will provide a healthful and safe environment for its employees and community neighbors and will monitor and evaluate employee health status, determine and monitor workplace factors affecting employee safety and health, comply with Monsanto workplace exposure guidelines and with governmental safety and health regulations, review major capital projects to protect the health ofpeople at work and in the community.
PROGRAM
1. Continue to perform periodic on-site surveys of worldwide operations to evaluate total safety, occupational health, and industrial hygiene status. Utilize observations and
. recommendations to achieve and maintain regulatory and code compliance, attain appropriate technological sophisti cation, reduce the probabtiity of accidents of all types, and further employee safety and health education. Generally assist sites in attaining year-to-year reductions in employee injuries and property losses. Optimize
' health surveillance programs to identify and prevent occupational illnesses.
2. Achieve and maintain compliance with governmental regulations and Monsanto guidelines as they relate to facility design, safe work practices, workplace exposures, health surveillance, and community safety and health in each country in which a Monsanto facility is located. If regulatory guidelines are unavailable or inadeqtiate to protect worker health, Monsanto will establish guidelines where appropriate.
3. Monitor and evaluate the effect of work exposures on employee health by providing health surveillance in all locations, with a goal of offering periodic examinations for all employees. Special emphasis must be given to implementing scheduled health surveillance examina tions for those employees routinely exposed to hazardous chemicals in the workplace. These examinations will be conducted by Monsanto or contract health professionals in accordance with the Occupational Medicine Program . defined by the Department of Medical and Health Sciences.
4. Collect and enter workplace materials, worker exposure, work history and employee health assessment data into the MEHI/MARS data base which will be used to perform epidemiological and other appropriate studies evaluating worker health to enhance worker protection.
5. Continue workplace surveillance to identify potential health risks, evaluate risks based on current toxico logical information and initiate appropriate safeguards to protect the health of employees.
6. Establish guidelines for use in classifying and recording injuries and illnesses to monitor company-wide perfor mance and adherence to federal regulations regarding recordkeeping. Issue monthly summaries of appropriate statistics, and various publications designed to improve
. awareness and to communicate relevant technologies to the workplace. Develop understanding of the causation of accidents and the techniques of accident prevention.
7. Provide corporate safety and industrial hygiene reviews
on design, startup, and operational issues for major new
installations and expansions.
8. Participate relative to safety and health through trade associations, other cooperative endeavors of the chemical and manufacturing industries and professional associations.
9. Provide employee training, orientation and education in safety and health.
10. Contract employees should receive any required surveil lance and safety and industrial hygiene indoctrination in accordance with Monsanto's Contractor Health and Safety Guideline.
(Revised and Approved by Environmental, Safety & Health Committee April 25, 1989.)
OSW 117S68
MONSANTO COMPANY
SECTION 4
Pace I
WATER PCB-SD0000021405
M
uu
WORLDWIDE GUIDELINE
#5
OUTSIDE PROCESSORS
Select companies for support of Monsanto operations -- through product conversions, custom manufacture, formulating, by-product sales, waste management, and other services supporting Monsanto businesses -- which will operate with concern for worker safety, regulatory compliance, community protection and protection of the environment.
PROGRAM
1. Monsanto will utilize only outside processors which have been selected and periodically assessed to assure:
(a) Their ability to adequately protect the public, employees and environment from any effect of Monsanto chemicals, products or wastes.
(b) Their compliance with all applicable laws and
regulations.
.
(c) Their knowledge of potential hazards and any applicable manufacturing requirements associated with Monsanto materials handled.
(d) Their use of approved waste disposal methods and locations, with recordkeeping of all material use and waste disposal.
2. Selections and assessments shall be documented and approved by the Operating Unit Director of Environmental Operations and an appropriate contractual arrangement shall be established with each firm prior to startup of operations.
3. Outside "processors" include firms which provide services related to Monsanto chemicals, products or wastes. "Primary" firms will receive an on-site assessment, management approval, and a written contract.
Secondary firms should be'assessed and be subject to
approval and contracts when high hazard materials or
Class B poisons are involved, or whenever the
situation involves a significant risk.
-
Primary services include:
Conversions Processing Blending Formulations Material Recovery/
Reclaiming
Tank Car Cleaning1 Barge Cleaning' Drum Cleaning/Reclaiming' Waste Material Sales Waste Hauling (including oil) Hazardous Waste Disposal
Material Purification Packing or Repacking Bulk Truck Geaning1
Waste Oil Disposal Waste Oil Reclaiming Transformer Retrofill
'Applicable w kaxardous products or Monsanto owned or teased vehicles.
Secondary services include:
Bulk Terminals Transloading Fulfillment Houses Packaged Goods Warehousing Non-hazardous Waste Disposal Vessel and Equipment Geaning
Excepted are services performed by established major chemical firms (approved by the Unit Director of Environmental Operations),.publicly owned treatment works, sales of wastes which are equivalent to virgin chemicals in commerce and transformer retrofill where wastes are retained under Monsanto control.
4. Assessments are to be performed prior to initial use and at a frequency recommended in the prior assessment (normally one to three years).
5. MCC Environmental Engineering maintains a corporate-wide database of all outside processors to avoid redundant assessments and contracts and to facilitate use of approved contractors.
6. The above program elements will be implemented at ex-U.S. locations, but with modifications as necessary to reflect local limitations, restraints to compliance, and the extent of Monsanto's operating control. Status and direction of the local program will be reviewed in planned environmental audits of these facilities.
(Reviewed and Approved without change by Environmental Safety <fc Health Committee April 25. 1989.)
MONSANTO COMPANY
DSW 117569
SECTION 5 Page I
WATER PCB-SD0000021406
MONSANTO
From (Name-Location-Phone) M. A. Pierle - G4WT/J. D. Anderson - F2WA
Date:
Subj: Ref: To:
March 22, 1990
i
Management of Outside Processors
.
See Attached Distribution
cc: E. N. Brasfieid R. G. Dahlen A. F. Fitzgerald G. M. Francx J. C. Hunter III T. H. Laffere R. G. Potter D. B. Price Jr. F. E. Reining D. L. Sliney W. H. Slowikowski C. A. Sweets J. L Tuley H. L. Williams M. W. Winkel
G5WA G4EM G5NV
5040 G4EA G4NJ G4NH G5NG G4NR G4NJ G4NA G4EA G5EA G4NI G5NA
In order to bring focus and strength to Monsanto's management of the use of outside processor services, we are making certain organizational changes within the MCC Operations group.
Monsanto environmental guidelines (attached) call for an effective program to assure that those providing outside services do so in a manner similar to that which Monsanto would employ if it chose to conduct the service itself.
To date, management of Monsanto's effort to assure compliance has been substantially decentralized with responsibility for conformance placed with the requestor of the service. Progress, when measured against the performance criteria within Monsanto's worldwide guideline, has not been at the desired
level.
In light of the need.to Improve the overall results of the program, a total quality team was established in 1989 to determine ways of improving the system. All functions were represented. The group extended its analysis by conducting a Business Process Management review. Deficiencies were examined and recommendations were made. These recommendations have been reviewed
and approved by MCC management.
To enable conformance with the guideline, three positions within MCC
Operations will provide coordination and services in concert with all .those
requesting outside processor services.
DSW 117570
WATER PCB-SD0000021407
2
1. Manager. Toll Manufacturing (Ed Moore)
This on-going position is responsible for the selection of toll (custom) manufacturing suppliers and the negotiation, monitoring and maintenance of contracts associated with these toll manufacturing arrangements. Included in the responsibilities of this position and most pertinent to this summary is the "providing of environmental and safety audits'* for all outside tolling arrangements.
2. Manager. Eouipment Disposal and Waste Disposal Contracting
(John Nolle)
.
This is not a new position, but rather an expansion of responsibilities of the prior position of manager, Equipment Disposal. This position will include the following responsibilities associated with waste disposal:
a) Defines and negotiates national waste contracts with firms that ' provide such services, to reduce and minimize costs through . corporate volume leverage to control Monsanto's off-site disposal costs. Primary areas include waste disposal services (incineration, landfill, medical, waste oil, etc.).
b) Serves as functional manager and corporate focal point for all national environmental service contracts Including day-to-day problem solving.
c) Develops opportunities to reduce waste disposal costs through prudent contract management.
d) Develops and negotiates master terms and conditions agreements with waste processing firms to insure Monsanto has appropriate contractual/legal protection.
e) Maintains strong functional ties with outside processor auditing manager to ensure audits and reaudits of outside processors are current lor all existing or proposed contract vendors.
3. Manager. Environmental Auditing (Gerald Rinaldi)
This is a new position In MCC Environmental Operations. The position
will ensure that outside processors meet Monsanto requirements for
financial responsibility, insurance, environmental compliance, industrial
hygiene, and worker health and safety as defined In ESH #5 by
coordinating the overall compliance system while relying predominantly
on existing plant resources to conduct the actual audits.
~
OSH 1.175 7J.
WATER PCB-SD0000021408
3
It should be obvious that .these three managers, plus appropriate resources In environmental and manufacturing assignments, will need to work closely together for Monsanto to meet its obligations and responsibilities in these most important areas. Your cooperation will be most appreciated.
Jamds D. Anderson Director, Purchasing
_____________ Michael A. Pierle
Director, Environmental Operations
A
OSH 1175.72
WATER PCB-SD0000021409
S. Abdou-Sabet
L. Adams J. W. Adams C. A. Balan L_ Beach R. J. Belle H. W. BerTy J. E. Bishop W. J. Board L. J. Boesch J. R. Bohrer W. J. Boyle P. Brezovec E. S. Brimer 0. R. Caldwell R. W. Ceyanes R. L Cheever J. J. Christian P. Clarke J. E. Crick R. J. Cushing . N. L Davis J. K. Davis D. K. Denner D. C. Dieterich M. P. DiGiovanni B. Dmuchovsky H. B. Driscoll . J. P. Dushney R. D. Ellis G. M. Ellsworth H. B. English E. A. Fay R. L Fields R. J. Fissmer M. R. Foresman V. M. Franchettl W. L Friehs R. C. Gary R. Geddes W. H. Ghetti M. E. Gibbs R. W. Graham M. B. Gray C. M. Grice M. N. Hanson T. S. Hardy H. P. Harris L F. Hebert B. D. Heckenberg F. L Hiller D. C. Hoegel S. A. Holmes C. C. Holzwarth K. S. Hood D. 0. Hummel
1010 1155 1690 1500 1260 G5NL 1410 1900 . 1690 G5NV F2WA 1740 1050 1760 1418 * 1200 1760 1760 1260 F2WA 1410 F2WB Fovil-Foley 1060 1150: 1090 F2WB G4NA 1410 1010 1775 G5WA 1290 C2NJ G5EA G4WT 1870 F2EE Fovil-Foley 1850 1080 R4B
Rock Springs 1200
- 1440
1918 1050 G4NA 1690 F1WE 1080 1290 1090 1090 1793 1290
DISTRIBUTION
W. M. Hunt J. P. Hyland T. G. Iversen E. S. Jamro G.L Johnson R. Jones R. N. Jones R. H. Joslin D. M. Kalbfteisch M. J. Kausch C. K. Keffer J. F. Keliher T. M. King 0. A. KJingler H. E. Knoop J. V. Kocurkovic D. S. Krawczyk M. A. Kulig J. A. Labanosky R. E. L Lamkin J. H. Lane M. D. Lauman R. E. Lawyer M. C. Lewis J. D. Leyerle D. M. Light S. J. Longfield K. J. Lott E. J. Mackie J. C. Marshall V. T. Matteucci M. D. McClendon M. W. McCombs C. M. McCullough J. T. McKean G. L. McKee T. R. McNeely N. B. Miller E. L Moore E. L Moore C. R. Murrell D. D. Musch G. S. Narsh R. J. Nichols J. S. Noble J. W. O'Brien G. E. O'Connor J. C. Ochsner . W. A. Ott R. P. Panasiewicz L P. Paradis W. W. Perdue K. M. Perica D. L. Petersen R. G. Pier A. L Pighin
; '
J L
M3G G4WT G5WA 1870 1440 1060 G5WA G4WS 1740 N2G C2SB G5NV 04C F2WD 1918 F1WG 1700 1870 1080 G5NV 1020 1850 1260 1870 F2WA 1670 1720 1850 G5WA 1670 G5NR 1560 1740 1850 1670 G4NC 1060 1250 F2WB F2WB 1155 1918 1900 1630 U4C 1260 F1WF 1540 1020
1500 G4WS 1220 1200 1683 &5NA 1540
-DSW 117573
WATER PCB-SD0000021410
A. J. Politte C. A. Pratte J. C. Rademaker
D. C. Ranson J. M. Ray S. D. Reiners W. S. Richey R. F. Riek G. M. Rinaldi
A. Ristic S. J. Robinson
C. J. Rogers J. F. Rohr L R. Rutledge R. F. Sackett D. E. Schoeffel A. R. Schroeder J. E. Schweitzer
M. A. Scott R. V. Sharp C. A. Smith J. 0. Smith D. E. Snowbarger R. W. Spiller M. A. State D. W. Stegan D. C. Stocker D. H. Stockton R. H. Talbert P. Thigpen J. L Thomas J. M. Tissue J. C. Trube A. C. Tuk C. Vance T. E. Warborg F. C. Weaver C. F. Weingartner
G. Wildsmith J. G. Wiley D. Wood
1720 F2WA 1050 1020 F2WA M3G 1220 1010 G4WT
1500 t G5NA
1440 1150 1793 1760 F2WD 1900' 1720 1700 1200 1793 1740 1683 G5NA 1900 G4NA G5NG 1220 1700 1150 1690 1200 F2WA 1670 1752 1010 1010 G5EC G5WA
1690 G5NL
OSH 117574
' WATER_PCB-SD0000021411
n_n InJ
WORLDWIDE GUIDELINE
#6
PRODUCT STEWARDSHIP
Monsanto products and intermediates will not present an unreasonable risk of barm to human life or health, or to the environment when they are properly handled, transported, used or disposed. Stakeholders will be provided information regarding handling, storage, use and disposal of Monsanto products.
INTRODUCTION '
Employees, customers and the community are all important stakeholders that are directly afTected by Monsanto's product stewardship programs. Inherent in these programs is the responsibility for assessing, managing, and communicating the risks associated with the products and intermediates Monsanto manufactures or markets or plans to manufacture or market.
Product assessments are at the heart of this process and involve judgments by specialists about the level of risk borne by stakeholders as a result of manufacture, 1 processing, distribution, use and disposal of a product. They integrate data on effects, (such as toxicology, epidemiology, and medical observations), with product composition and exposure information (such as industrial hygiene monitoring, and environmental fate). For each Monsanto product or intermediate, we need enough data or information to reach a supportable conclusion that under reasonably anticipated conditions of handling and use, the product does not pose an unreasonable risk to those who may be exposed or the environment. We must recognize that our stakeholders have a voice in this decision process. It is our responsibility to provide stakeholders with information such as labels and Material Safety Data Sheets, which will permit them to have knowledgeable input into the process. Our risk management actions must reflecj.stakeholder input.
i'
PROGRAM
1. All new product candidates and new process inter mediate candidates will be assessed and managed as detailed below. Note: in view of the unique charac teristics of articles, they will be handled separately from this program.
a) All local, national and international product regulatory requirements will be satisfied in a timely fashion during project development.
MONSANTO COMPANY
b) R&D materials utilized in the laboratory will be handled according to Prudent Laboratory Practices (e.g.. National Research Council Guidance, Monsanto Research Center Policies and Procedures, or similar).
c) New R&D products and process intermediates, that are either,
i) shipped to customers, non-laboratory facilities or laboratories covered by the OSHA Hazard Communications Standard or,
ii) produced in significant quantities (e.g., U.S. regulations define significant quantities as "quantities in excess of I00Kg/ycar") or,
iii) manufactured or handled in non-laboratory facilities,
will have a completed product safety review (i.e., one or more of the following: ER-200, EC-201, pilot plant safety audit or equivalent. Institutional Biosafety Committee Review) an appropriate label, and a Materia] Safety Data Sheet, or R&D equivalent.
d) New products, new process intermediates, and significant new uses of existing products will have a product assessment (EC-202 or equivalent), a Material Safety Data Sheet and a shipping classification (TF-837 or equivalent) completed before commercialization.
e) Material Safety Data Sheets for new products and process intermediates will be made available to all persons engaged in R&D commercialization of these materials.
2. All commercial products, process intermediates or product families comprised ofthese materials, will have ongoing product assessments, risk management and hazard and risk communications.
DSW 117575
SECTION 6
WATER PCB-SD0000021412
PROGRAM (continued)
a) Material Safety Data Sheets or equivalent will be
developed for all Monsanto products and process
intermediates. Material Safety Data Sheets will be
provided to employees and customers and made
available to other stakeholders in an appropriate
language. All issued Material Safety Data Sheets
will be reviewed when significant new information
affecting the product or intermediate becomes
available. At a minimum, reviews will be
.
performed every five years. Material Safety Data
Sheets will be updated as appropriate as a result of
these reviews. Records of Material Safety Data
Sheet recipients will be maintained, where
practical.
b) Product files for all products or product families . will be maintained. The product file may include
the following:
Appropriate Materia] Safety Data Sheets, references to relevant literature or internal reports, relevant information on composition, physical properties, manufacturing processes, principal by-products, protective measures and exposure information.
A critical review of health and environmental effects and exposure information, such as
' EC-201, EC-202, Monsanto Work-Place
Permissible Exposure Guideline (MWPEG) Reviews, Health Effect Reviews and Toxicology Reviews.
c) Information contained in product files will be used for business decisions, government interactions, public communications and other product management activities.
3. Product Stewardship is the responsibility of the business units. Each operating company, free-standing division or world area will assign an individual(s) the responsibility for assuring that this Guideline program is met.
Guideline oversight is the responsibility of the Corporate Environmental Policy Staff.
Units of the corporate staff (Environmental Policy Staff, Safety and Environmental Health, and others) and business units are jointly responsible for developing information needed for product ' assessments. This includes regular periodic reevaluation of data available in light of new information relevant to the product.
(Revised and Approved by Environmental, Safety & Health Committee April 25, 1989)
SECTION 6 Pace 2
OSW 1175.76
WATER_PCB-SD0000021413
DISTRIBUTION
R. E. Ackerman I. Andrer
U4C 5040
R. M. Bannister J. W. Barnett
D. Barrett
A3ND A3ND
U4C
N. C. Boggs II E. J. Bollanas D. P. Brown J. R. Condray J. E. Downes K. E.. Storm P. A. Easterday
C- Elmer T. F. Evans J. D. Felder
J. J. Ferguson
M. R. Foresman
,
E2NK ' 5300
F2EC A3NA G4WR A3NL A3NL A3NA A3NA G4WR 5000 G4WT
B. R. Friedlander
A3NA
B. J. Gilhousen J. S. Harding
E2NK 5040
R. L. Harness
C2SB
A. D. Hatten
G4WR
C. E. Healy
A3ND
J. L. Henshaw
A3NL
B. J. Hill J. P. Hyland
G4WR G4WT
J. R. Jackson
5040
E. P. Jannsen -
5270
A. J. Janusz
U4C
F. R. Johannsen
A3ND
G. M. Johnson
A3NL
R. H. Joslin
G4WS
S. P. Krchma
E2NG
C. J. Larsen
5040
R. I. Lennox
A2NA
G J f Levinskas
A3ND
C. D. Mailoch
A3NA
J. N. McGuire
G4WM
D. E. McKinney
A3NG
J. P. Mieure D. G. Montgomery
G4WR G4WR
M. J. Murphy
A3NL
R. S. Nair
- A3ND
J. H. Nisbet
5050
J. S. Noble
U4C
E. F. Ogu
A3NL
L. P. Paradis
G4WS
C. Paton/D. Abresch 5510
C. O. Patterson
F2EA
C. R. Perry
5040
M- A. Pierle
G4WT
M. Plotnick
5090
D. J. Randall D. B. Redington
A3NG A3NA
M. D. Rhine-Jones V. L. Rhodes
G4WR G4WR
K. T. Richardson G- M. Rinaldi E. C. Robinson R. D. Short P. H. Smith W. L. Smull G. S. Spies M. W. Stevens
C. Strang R. L. Walter M. F. Weishaar C. A. Wiltshire P. C. Wright
5040 G4WT A3ND A3ND E2NK G4WM A3NL A3NG A3NL A2NA G4WM 5040 E2NK
XISH 117577
WATER PCB-SD0000021414
Monsanto
FROM (mahe-iocatiow-phoke)
OCT i s ?99G
F. E. Kearney - St. Louis, G4WT - 4-314 6
DATE: SUBJ: REF: to:
October 12, 1990
cc:
MCC NEW PRODUCT INTRODUCTIONS ENVIRONMENTAL AND RELATED FOLLOW-UPS '
See Distribution
Monsanto's policy is to sell only those products that do not represent an unreasonable risk of harm when properly handled, etc. (Attachment 1). The final authority for permitting sampling and/or sale of new products rests with the Department of Medicine and Environmental Health "DMHS"), whose procedures are described in DMHS "Health and Environmental Compatibility Assessment of Monsanto Products, A Guide to the Use of Department of Medicine & Environmental Health Data Sheets 131-200, EC-201 and EC-202". This policy and procedure apply to Monsanto products worldwide.
At each stage of the DMHS approval process (ER-200 limited to bench
scale R&D sampling, EC-201 for any sampling, and EC-202 for
commercialization), there are follow-up steps to be taken. The
attached procedure (Attachment 2) is newly created for MCC use
worldwide. Please insure that others in your organization who are
involved in any aspect of new product introduction are also given
copies. Your help in this as well as in insuring compliance are
appreciated.
.
If you have any questions, please contact your assigned Manager,
Product Safety.
.
/pam Attachments
F. E. Keaarrnneayv I
DSW 117578
WATER PCB-SD0000021415
PROGRAM (continued)
a) Material Safety Data Sheets or equivalent will be
developed for all Monsanto products and process
intermediates. Material Safety Data Sheets will be
provided to employees and customers and made
available to other stakeholders in an appropriate
language. All issued Material Safety Data Sheets
will be reviewed when significant new information
affecting the product or intermediate becomes
available. At a minimum, .reviews will be
performed every five years. Material Safety Data
Sheets will be updated as appropriate as a result of
these reviews. Records of Material Safety Data
Sheet recipients will be maintained, where
practical.
_
b) Product files for all products or product families will be maintained. The product file may include the following:
Appropriate Material Safety Data Sheets, references to relevant literature or internal reports, relevant information on composition, physical properties, manufacturing processes, principal by-products, protective measures and exposure information.
A critical review of health and environmental effects and exposure information, such as EC-201, EC-202, Monsanto Work-Place Permissible Exposure Guideline (MWPEG) Reviews, Health Effect Reviews and Toxicology Reviews.
c) Informadon contained in product files will be used for business decisions, government interactions, public communications and other product management activities.
3. Product Stewardship is the responsibility of the business units. Each operating company, free-standing division or world area will assign an individual(s) the responsibility for assuring that this Guideline program is met.
Guideline oversight is the responsibility of the Corporate Environmental Policy Staff.
Units of the corporate staff (Environmental Policy
Staff, Safety and Environmental Health, and others)
and business units are jointly responsible for
developing information needed for product
.
assessments. This includes regular periodic
reevaluation of data available in light of new
information relevant to the product.
(Revised and Approved by Environmental, Safety & Health Committee April 25, 1989) ,
SECTION 6 Page 2
O.S* 117580
WATER PCB-SD0000021416
(3) has been submitted already to EPA under another undatcr/ reporting provision of l) TSCA, or 2) iom a char authority that is administered by EPA.
(A) is containad in a fonal publication/raport or a formal
statsaent made availabla to tha ganaral public by another Federal agancy.
(5) is corroborativa (in ttiu of, for example, routa of axpoiure, doa, species, time to onset, severity, apaciaa, strain, ate.) of a Tall-aitabllihad adverse affect.
It ia important to note, hovavar, that information that navly
idantifiaa a carious toxic affact at a lower dosa level fer
axaapla, or confirms a carious affect that vac prrrioocly only
compacted, ic
concidarad by EPA to ba corroborativa and
should ba raportad undar Saction 8(a) of TSCA.
(6) is information for which tha EPA Administrator has waived compliance with TSCA in general or Section 8(a) specifically upon a request and detarmination of the President of the United States that such a waiver is required in the interest of the national defense; Section 22 of TSCA outlines the procedures by which such waivers are to be re-7-------
With regard to item (2) on the preceding page, EPA believes that for tha purposes of Saction 8(a) reporting, a subject parson need not report information that is obtained from well-established/vell'recognized scientific journals, such as those typically abstracted in a) major computerized abstract data bases, or 2) publications such as current Contsnti published by tha Institute for Scientific Information (ISI), Inc. (Philadelphia, Pennsylvania). Similarly, information that is obtained from major U.S. news publications (a.g., newspapers or news magazines with national circulation) cr nationally broadcast U.S. radio and/or television news reports typically need not be submitted to EPA undar Saction 8(a) of TSCA. However, with regard to information obtained from lesser known scientific journals, or from other magazines, newspapers, radio or talsvision reports, a subject person must have actual knowledge that EPA has bean adequately informed about such information.
Specifically with regard to item (4) ,
it cannn- be
automatically assumed that the Agency has been adequately informed
about informatifin in a report or study by another Federal or other
governmental aqency if the report or study has not been formally
published or otherwise released to the general public. Therefore,
if a person obtains (i.s., possesses or knows of), for example,
certain unpublished Section 8(a)-reportable information from a
study that is conducted by or for an agency of the U.S. Government
(other than EPA), that person must consider tha need to immediately
submit those findings under Section 8(e). Since 1977, EPA has
received a number of Section 8(e) notices filed by companies who
had obtained unpublished results of studies conducted by or for
other Federal or other governmental agencies. In most cases, such
submissions are limited to 1-2 pages and the Agency immediately
establishes direct contact with tha responsible agency to minimize
or eliminate the company's Section 8() reporting burden.
DSV^ 1 1 7 6 2 2
WATER PCB-SD0000021417
pofll ggpoRTrsQ to ajoteh*
srr jictipt tiz) RZQUiitacgyrai
Mandatory or other reporting of information to another agency dos . no- ,atiafy a company`a obligation to iaaadiataly inform EPA undar
Saction 8(a) of TSCA.
TKinr MUST BSCTIOT 8(1) IHTORXRTIOy BI REPORTED?
A parson is considarad to hava discharged tha TSCA Saction 8(a)
reporting obligation JLX the information is racaivad at EPA Haadquartars in writing within 15 working days aftar tha parson
obtainad tha information. Ralavant or significant supplemental
data obtained aftar an initial Saction 8(a) submission should also be reported in writing to EPA immediately (i.e., within 15 working
days). The reader** attention is directed to THAT doel to TERM
"obtxtts rmToaxATTOT" mxrr found on Page 6 of this reporting
guide.
'
Par an "Emergency Incident of Environmental Contamination" (EXEC), a telephone call to the appropriate EPA Regional Office must b* placed immediately (i.e.r as soon as reasonably possible); these phone numbers are given in the next section of this guide. A written follow-up report must also sent to EPA Headquarters within 15 working days of the date oh which tha telephone report was made.
HOT KP8T 8ECTIOT (El HTPORXRTIOH Bf REPORTED?
Section 8(e) submissions must be transmitted to EPA in a manner that permits the Agency to verify receipt of the submission (e.g., certified or registered mail). 'In addition, the submission must state clearly that it is being provided under Section 8(e) of TSCA. Purther, the submission must contain the name, title and telephone number of the person sending the information, the name and address of the establishment with which the reporting person is affiliated, the name(s) (including Chemical Abstract Service (CAS) Registry Humber(s), if known) of the subject chemical(s) and a summary describing the nature of adverse effects or exposure being reported together with the source of any supporting technical data.
Por an "Emergency Incident of Environmental Contamination" (EXEC), the initial telephone report must provide the time and location of the incident and as much of the above information as is known at tha time. A written EXEC follow-up report to EPA Headquarters must contain the same types of information that are required in a nonEIEC initial Section 8(e) submission.
OSW 117623
3 of 3
WATER PCB-SD0000021418
OVERVIEW OF TSCA SECTION 8(e)
What 'l3^?^0XySeaCioTT^16yeV?
TSCA Section 8(e) requires that:
"Any person who manufactures, processes, or distributes in commerce a chemical substance or mixture and who obtains information which reasonably supports the conclusion that such substance or mixture presents a substantial risk of injury to health or the environment shall immediately inform the Administrator of such information unless such person has actual knowledge that the Administrator has been adequately informed of such information."
NOTE: The term chemical substance does not include substances used exclusively as food, food additives, drugs or cosmetics if regulated by the FFDCA, pesticides if regulated by the FIFRA, and articles.
The meaning of virtually every word of. this paragraph has evolved over the years, since passage of TSCA in 1976.
Unlike most other sections of TSCA, EPA has not issued regulations imple
menting 8(e), and therefore you won't find it in the Code of Federal
Regulations.
Interpretative guidance was first issued by EPA on March 16, 1978 (43 Fed.
Reg. 11110; hereinafter referred to as S8(e) Guidance), and supplemented over
the years by:
'
%-
status reports of $8(e) submissions;
enforcement cases; and, letters to individual companies.
In formulating the 8(e) provision. Congress responded to a concern that a
number of companies had suppressed information about the cancer-causing nature of certain chemicals. Examples described during the hearings included vinyl
chloride and bis-chloromethyl ether. S8(e) was designed to ensure that this
type of information would receive prompt attention by the EPA. Current interpretations by EPA go far beyond these examples. (See below.)
"Persons" who manufacture, process, or distribute chemical substances or mixtures must report. Trade associations may provide a report for their
members, although they are not required to do so under S8(e). Similarly, testing laboratories have no reporting obligations under S8(e), even if they
are in possession of reportable information.
A company can relieve individual officers and employees of their obligation to
report potential S8(e) information to the Agency by:
"Establishing, internally publishing, and affirmatively implementing
procedures for employee submission and corporate processing of
pertinent information."
OSW U7&24
WATER PCB-SD0000021419
-2-
When^Hust^Pefs^^
EPA must be "immediately informed" by telephone within hours of emergency incidents of environmental contamination, with a written follow-up sent within
IS working days after the incident. In its S8(e) Guidance, EPA stated that other S8(e) information must be submitted "not later than the ISth uorking day after the date the person obtained such Information."
EPA $8(e) Guidance .states that "a person obtains substantial risk Information
at the time he first comes into possession or knows of such information." Further, "an establishment obtains information at the time any officer or employee capable of appreciating the significance of such information obtains it" (emphasis added).
A "substantial risk of injury to health or the environment* is a risk of considerable concern because of:
(a) the seriousness of the effect; and
(b) the fact or probability of its occurrence.
The S8(e) Guidance provides the following examples:
(1)
Any instance of cancer, birth defects, mutagenicity, death or serious or prolonged incapacitation, including the loss of or inability to use a normal bodily function with a consequent relatively serious impairment of normal activities if one (or a few) chemical(s) is strongly implicated.
(2)
Any pattern of effects or evidence which reasonably supports the conclusion that the chemical substance or mixture can produce cancer, mutation, birth defects or toxic effects resulting in death, or serious or prolonged incapacitation.
The Agency has also defined "substantial risk" in terms of serious or pro longed incapacitation. Animal toxicology reports are by far the most frequent
8(e) submissions. These, of course, provide the best indication of the toxic
response of a test chemical in humans (short of actually testing the chemical in humans).
Normally, standard acute toxicology tests are not subject to S8(e) reporting,
unless something very unusual and/or unexpected is observed. For example, a
rat peroral LDS0 of 0.5 mg/kg for "Chemical X" would be unusual and unexpected
if chemicals closely related to it had rat peroral LDSQ*s in the.1 to 4 g/kg
range. As a practical matter, any unusual or unexpected result should be
given consideration for S8(e) reporting, and any results of a "serious" nature (as defined in the S8(e) Guideline) should also be considered for S8(e)
reporting.
'
J3SW 117625
WATER_PCB-SD0000021420
-3-
The Agency guidance on $8(e) reportability hae evolved over the years, as reflected in both its S8(e) "Status Reports" and other documents, including
litigation papers and letters to various companies which address specific
8(e) issues. For example, the S8(e) reportability of developmental and
neurotoxic effects was addressed in a 1988 letter to Monsanto.
Regarding the S8(e) reportability of mutagenicity results, the Agency's
current position on in vitro tests (such as the Ames test) is:
"Although a positive in vitro genotoxicity finding, when considered
alone, may not be sufficient to offer reasonable support for a
conclusion of substantial risk..-EPA does believe that a single
positive genotoxicologic finding is of value in assessing the
possible risk(s) posed by exposure to the tested chemical substance
or mixture." (8EHQ--0687--0677)
However, when the exposure potential is-very high (as, for example, with a copy machine toner), the Agency has accepted a positive Ames result as an
indication of substantial risk (8
EHQ-0780-0351). Also, when combined with other information (in vitro tests,
for example), a positive Ames result could be 8(e) reportable.
In a risk assessment context, "risk" is generally defined as a function of
hazard and exposure. Thus, it would be logical to conclude that "substantial
risk" (in the TSCA S8(e) context) would involve a function of hazard (such as
a toxicology finding) and exposure (actual or potential). Such is not the
case under TSCA S8(e).
.
The Agency has essentially eliminated the role of exposure in the determina tion of substantial risk (with few exceptions). Serious health effects far
outweigh exposure considerations. Indeed, the $8(e) Guidance states that:
"the mere fact the implicated chemical is in commerce constitutes sufficient evidence of exposure" ("commerce" has also become quite broad in its meaning, and includes R&D activities).
This is addressed in the $8(e) Guidance. Information can come from designed
well-controlled studies, as well as from undesigned uncontrolled circum stances. The evidence does not have to be conclusive; it should, however, reliably ascribe the effect to the chemical.* 1
The $8(e) Guidance provides the following examples:
DSW 117626
(1)
Widespread and previously unsuspected distribution in environmental media, as indicated Ln studies (excluding materials contained within appropriate disposal facilities).
(2)
Pronounced bioaccumulation. Measurements and indicators of pronounced bioaccumulation heretofore unknown to the Administrator (including bioaccumulation in fish beyond 5,000 times water
WATER_PCB-SD0000021421
-4-
concentration in a 30-day exposure or having an n-octanol/water partition coefficient >25,000) should be reported when coupled with potential for widespread exposure and any nontrivial adverse effect.
(3)
Any nontrivial adverse effect, heretofore unknown to the Administrator, associated with a chemical known to have bio accumulated to a pronounced degree or to be widespread in environmental media.
(4)
Ecologically significant changes in species' interrelationships, that is, changes in population behavior, growth, survival, etc., that in turn affect other species' behavior, growth, or survival.
Examples include:
(i)
Excessive stimulation of primary producers (algae, macrophytes) in aquatic ecosystems, e.g., resulting in nutrient enrichment, or eutrophication, of aquatic ecosystems.
-
(ii)
Interference with critical biogeochemical cycles, such as the nitrogen cycle.
(5)
Facile transformation or degradation to a chemical having an unacceptable risk as defined above.
There have not been many environmental S8(e) submissions to date. While EPA
guidance in this area is very limited, it would appear that risk can be considered in determining reportability of environmental information. The "trigger words" to remember in this context are:
widespread and previously unsuspected; pronounced bioaccumulation; and, unusual, unexpected, and nontrivial.
An example of a reportable study would be extensive data on TCOD ("dioxin") in river water sediments and fish, which was both widespread and unsuspected. A nonreportable study example would be a study which describes ambient and stack sampling results, with no indication of being widespread and unsuspected.
EPA S8(e) Guidance defines this as:
OSH 11762.7
"Any environmental contamination by a chemical substance or mixture to which any of the above adverse effects (i.e., previously described environmental effects subject to 58(e)) has been ascribed and which because of the pattern, extent, and amount of contamination:
(a)
(b)
Seriously threatens humans with cancer, birth defects, mutation, death, or serious or prolonged incapacitation; or,
Seriously threatens nonhuman organisms with large-scale or
ecologically significant population destruction."
WATER PCB-SD0000021422
-5-
^Ha1WnTonnI't:t;aiiP,l
'(^ii&&ii2S8&4&2aS'
Information need not be reported if it:
(a) Has been published by EPA in reports.
(b) Has been submitted in writing to EPA pursuant to mandatory reporting
requirements under TSCA or any other authority administered by EPA
(including FIFRA S6(a)(2); see 8(e) Guidance). This also includes timely (within 15 days) submissions under $8(d), 54, and S5 (PMN, SNUR).
(c) Has been published in the scientific literature and referenced by any one
(1) of six (6) defined.abstract services.
(d)
Is corroborative of well-established adverse effects already documented in the scientific literature, unless this information concerns emergency incidents of environmental contamination. (In its action against Union
Carbide concerning an alleged 8(e) violation, EPA essentially rendered
the definition of "corroborative" to mean replicative. As a practical matter rarely, if ever, would a new study "corroborate" a prior study because some parameter would almost always be different.]
(e) - Is contained in notification of spills or emergency releases under other Federal authority.
(f)
Applies to chemicals that are exclusively food, food additives, drug or cosmetic if regulated by FFDCA; pesticide (after EUP) if regulated by FIFRA; and article.
(8/20/90)
OSH 117628
WATER PCB-SD0000021423
MInJ PROCEDURE
i
TSCA 8(c) RECORDKEEPING: LITIGATION CLAIMS
DETAILED PROCEDURE:
Step I
Litigation complaints will be reviewed at the time of receipt by the law department for relevance to TSCA 8(c) recordkeeping. Criteria for this review include the following:
a) Is the claim against a Monsanto product or process?
b) Is the produces) in question one that is covered by TSCA, i.e., other than pesticide, herbicide,
food, food' additive, or pharmaceutical?
'
c) Is the claim a health or environmental claim?
If questions a, b and c are all yes, the claim will be sent to the DMHS occupational medicine group. Exceptions to this include: PCB claims which will be sent to the EPS/Product Safety Group for review and claims against MAP, Nutrition and Health Care Products which will be sent to these respective groups when the law department is unsure of the answer to question (b).
Step 2
The rrenparinnal medicine group of DMHS will review the litigation claims passed to them by the-law
department. The review will be based on EPA's definitions of "known human effect" and "significant
adverse reactions." (40 CFR 717) For environmental effects, DMHS may need to contact the appropriate
DEO for assistance. daiim that do not meet TSCA 8(c) criteria will be dropped from further TSCA review
of tins step. Those claims that m^r TSCA 8(c) criteria will be forwarded to the DRM, Toxic Substances,
for filing. PCB claims that
the 8(c) criteria will also be forwarded for filing.
Step 3
Claims meeting the 8(c) criteria will be .filed in the TSCA 8(c) file maintained by the DRM, Toxic Substances. This office will request a copy of the complaint "answer" from the law department.
Step 4
.
The law department will forward a copy of the complaint "answer" to the DRM, Toxic Substances for filing in the TSCA 8(c) file, along with the "complaint" The "complaint" and "answer" will constitute the TSCA 8(c) recordable "allegation" and "follow-up" for all litigation filings.
A block flow diagram of the TSCA 8(c) process for litigation complaints appears on the reverse side of this page. *
}
MONSANTO COMPANY
OSW 117629 PR3-Appendix 3.1
T
WATER_PCB-SD0000021424
TSCA 8(c) REVIEW PROCEDURE OF LITIGATION CLAIMS
Complaint
Drop
EPS PCB
8(c) Recordable "Complaint"
,, PCB
Law Department Review
Health and Environmental "Complaints"
li "Complaints" covered by TSCA
FIFRA Food and Drug
Non Health and Environment
Drop
Exemptions from TSCA not clear
MAP Nutrition Health Care
Drop
DMHS Medical , .
""
8(c) Recordable ' ' 1 "Complaint"
Do not meet 8(c) cntena
^ Drop
DRMTSCA Request
' 1 "Answer*
File "Complaint", in 8(c) file
*
Law Department
"Answer* *
'f
osw
DRMTSCA
File "Answer" in 8(c) file
PR3-Appendix 3.2
WATER_PCB-SD0000021425
PROCEDURE
^ RECORDING ALLEGATIONS OF SIGNIFICANT ADVERSE REACTIONS UNDER TSCA - U.S.
Monsanto procedure for handling the Recordkeeping Requirements of Final U.S. Environmental Pro tection Agency Rule Under Section 8(c) of the Toxic Substances Control Act (TSCA).
1. Abstract of Rule - Manufacturers and certain processors of chemical substances and mixtures must maintain records of significant adverse reactions to health or the environment alleged to have been caused by a substance, mixture, article, pfocess, effluent or emission.' These records are subject to EPA inspection.
Rule Reference - 40 CFR Part 717 (48 FR 38178 August 22, 1983)
Note: The Rule does not apply to pesticides, food, food additives, drugs or cosmetics when manufactured, processed or distributed for these uses.
2. Key Definitions - (See Section 717.3 of the Rule for complete listing of definitions.)
* a. "Allegation" means a statement made without formal proof or regard for evidence, that a chemical substance or mixture has caused a significant adverse reaction to health or the environment.
b. "Known human effect" means a commonly recognized human health effect of a particular substance or mixture described either in:
i. Scientific articles or publications abstracted in standard reference sources.
ii. The firms product labeling or material safety data sheets (MSDS).
However, an effect is not a "known human effect" if it:
i. Was a significantly more severe toxic effect than previously described.
ii. Was a manifestation of a toxic effect after a significantly, shorter exposure level than described.
iii. Was a manifestation of a toxic effect by an exposure route different from that described.
c. "Significant adverse reactions" are reactions that may indicate a substantial impairment of normal activities, or long-lasting or irreversible damage to health or the environment.
3. Exemptions from the Role that relate to Monsanto
a. Activities involving solely mining or other solely extractive functions.
b. Significant adverse reactions that are known human effects.
c. Significant adverse reactions to the environment directly attributable to incidents of environmental contamination that have been reported to the federal government under any applicable authority.
4. Who can receive an allegation?
Allegations can come from a variety of sources including: employees, contractors, customers and neighbors.
As a result, Monsanto's receiving network must be broad. Initial receptors include: plant, laboratory and other Monsanto location supervision; plant and other Monsanto location managers, the Monsanto medical community at all locations, the offices of the Operating Company Directors of Environmental Operations, sales and marketing contacts, switchboard operators at all locations and environmental network contacts.
5. Procedure for Handling Health or Environmental Allegations
The Monsanto Toxic Substances Control Act (TSCA) Section 8(c) procedure consists of a four-step review and decision process. (Note: A separate procedure for litigation claims will be used see Appendix 3.1. A determination thatft~an allegation is not recordable under the Rule can be made at any step in the process. The procedure is shown schematically on Appendix 3.2).
MONSANTO COMPANY
Post-It- brand fax transmittal memo 7671 oi pa*
TO K.v.l*
Co.
Co. f
OepC Fll *
Phono Co.
DSW 1J.76 3J.
: PR3-1
WATER PCB-SD0000021426
RECORDING .ALLEGATIONS OF SIGNIFICANT ADVERSE REACTIONS UNDER TSCA - U.S. (continued)
5. Procedure for Handling Health or Environmental Allegations (continued)
a. Step One - Each plant or other Monsantodesignated locations or laboratory will have at least one identified and trained TSCA Section 8(c) key contact. The Director of Environmental Operations (DEO) or designate from the appro-priate operating companies, representatives of the WHSA (World Headquarters Site Administration), and Director, Regulatory Management (DRM), Toxic Substances will serve as the key contacts for the General Offices. The DEO's have responsibility under this procedure for free-standing divisions and ' subsidiaries of which Monsanto owns 50 percent or more of the voting stock or other equity rights, or for which Monsanto has the power to control the management and policies of that firm. At Step One, all initial receptors will automatically transfer persons making oral allegations to the key contact at their locations. Initial receptors will also transfer written allegation to the key contact at their location. (There are two exceptions with respect to oral allegations: If the initial receptors are either members of the Department of Medicine and Health Sciences Occupational Medicine (DMHS-OM) group (physicians) or the DEO's office, then these individuals can judge at Step One if an oral allegation is excluded.) Decision Criteria for Step One: pesticides, food, food additives, drugs, or cosmetics are excluded. If a decision is made that the allegation is excluded, the allegatipn, if written, will be discarded and, if oral, will not be acted on under the Rule.
If the allegation is oral and not excluded, the key contact will inform the alleger that such allegation may be recordable under the Rule and request that the alleger submit a written and signed allegation to the key contact Monsanto Form 8(c)A, shown on Appendix 2, is available to be used for all employee related oral health allegations and can be used at the discretion of the DEO for external oral health allegations. All key contacts must note on a written allegation the date of its receipt -
b. Step Two - The key contact at a Monsanto location or the appropriate DEO for the General Offices will provide Monsanto employees with Form 8(c)A for oral allegations of health effects. Written allegations will then be reviewed by the key contact, who will then make a Step Two decision. The key contact will determine if the written allegation is exempted from the Rule using the criteria in paragraph 3 above. If a decision is
made that an allegation is exempt from the Rule, the allega-tion will be discarded. Otherwise, the allegation will be sent to the appropriate DEO for review.
c. Step Three - The appropriate DEO will serve as the coordinator for Step Three and Step Four activities. Allegations received from the location (plant, etc.) key contacts will be reviewed by the DEO and a Step Three decision made. A Step Three decision also will be made by the DEO or other General Offices key contact regarding allegations made to the General Offices receptors. If the Step Three decision is that the allegation is not recordable under the Rule, the allegation will be discarded. Otherwise the allegation will proceed to Step Four.
d. Step Four - The DEO will form a committee to make decisions with respect to allegations that must be recorded under the Rule. The committee will be chaired by the DEO and consist of appropriate members of DMHS-OM for human effects, appro-priate members of Environmental Sciences for environmental effects. Environmental Law and the DRM, Toxic Substances. If the decision is that the alle-gation is not recordable under the Rule, the allegation will be discarded. The DEO will provide feedback to the location key contact. If the Step Four decision is that the allegation is recordable under the Rule, then the DRM-Toxic Substances, will place the allegation and documents mandated by the Rule in the TSCA Section 8(c) file. The DEO will provide feedback to the location key contact.
6. Record keeping
The TSCA Section 8(c) file will be kept in the Office of the DRM Toxic Substances. The file structure will confirm to requirements of Section 717.15 of the Rule. Files pertaining to adverse reactions to health of employees will be retained for 30 years. Hies pertaining to other adverse reactions will be maintained for 5 years.
7. Communications
a. Disposition of written allegations will be communi-cated back to the individual making the allegation. The key contact will facilitate the communication.
b. A summary of the TSCA Section 8(c) procedure will be periodically communicated to all affected employees and updated, as appropriate.
(Reviewed and Approved: Environmental Safety and Health Committee. October 20. 1987.)
OSW 117632
WATER_PCB-SD0000021427
PROCEDURE
SIMPLIFIED FLOW DIAGRAM OF MONSANTO PROCEDURE FOR HANDLING ALLEGATIONS SUBJECT TO TSCA 8(c)
) Allegation qualifies for TSCA 8(c) recordkeeping. Put in 8(c) file in St. Louis.
MONSANTO COMPANY
STEP ONE: Decision
, t subject to TSCA 8(c) recordkeeping. Drop from process.
STEP TWO: Decision
Not subject to TSCA 8(c) recordkeeping. Drop from process.
OSW 117633
STEP THREE: Decision
Not subject to TSCA 8(c) recordkeeping. Drop from process.
STEP FOUR: Decision
Not subject to TSCA 8(c) recordkeeping. Drop from process.
PR3-Appcndix 1
WATER PCB-SD0000021428
PROCEDURE
ALLEGATIONS OF SIGNIFICANT ADVERSE REACTION TO HEALTH Toxic Substances Control Act, Section 8(c) 40 CFR Part 717
NAME OF ALLEGER:-----------------------------------------------------------------------
i
ADDRESS: (If doc employee)
______________________ ____________________________
SITE LOCATION:
----------------------------------------'
SITE ADDRESS:
DATE:-------- /--------- /
MO DAY Y*
SITE LOC. CODE-
(If health effect only): M [] F Q
YR. OF BIRTH:------------------------
Employer (if other than Monsanto):-------------------------------- --------------------------------------------------------- .--_--,--.--.----- f ) DESCRIPTION OF ALLEGED ADVERSE HEALTH EFFECT:
1. WHAT IS THE HEALTH EFFECT BEING CLAIMED?-------------------------------------------------------- ;---------------:------------
2. HOW LONG DID IT LAST?
3. HOW OFTEN HAVE YOU EXPERIENCED EFFECT?--------------------------------------------------------------------------------------
4. IN WHAT WAY DID IT AFFECT YOUR NORMAL ACTr/mES?--------------------------------------------------------------------
5. HOW WERE YOU EXPOSED?----------------------------------------------------------------:-------------------------------------------------------
WHAT SUBSTANCE, MIXTURE, PROCESS OR OPERATION DO YOU THINK CAUSED THE EFFECT YOU DESCRIBED:
1 a-v FOR COMPANY USE ONLY:
RECEIVED ON:.
MONSANTO COMPANY
BY:.
Signature _
OSH 117634
PR3-Appendix 2
WATER_PCB-SD0000021429
MInJ PROCEDURE
PREMANUFACTURE NOTIFICATION TO EPA UNDER TSCA - U.S.
Monsanto procedure for development of premanufacture notification (PMN) as required under Section 5 of the Toxic Substances Control Act (TSCA).
1. Abstract of Requirements - A PMN is required to be submitted to EPA for all new chemical substances at least 90 days before the substance can be manufactured for commercial purposes. A number of substances are exempted from these requirements including, but not limited to: drugs, food and food ' additives, pesticides, R&D substances, nonisolated intermediates, and substances on the TSCA inventory.
Final Rules Reference - 40 CFR Part 720.
2. Is a PMN required?
At a very early stage of a new product development, including isolated intermediates and new imports, several checks should be made to determine if a PMN will be required for the product.
a. Is the product (substance) exempt under TSCA? Responsibility: Operating Company Director,
- Environmental Operations (DEO) or designate.
Section 2(B) of TSCA exempts broad classes of substances such as pesticides, food, food additives, mixtures and others.
Section 5(h) exempts small quantities for R&D purposes and has provisions to exempt substances for test marketing low volume manufacture, and polymer manufacture.
Refer to TSCA law and regulations for details or contact Director, Regulatory Management (DRM), Toxic Substances.
b. Is the substance "new" under TSCA? (Is it on the ` TSCA Inventory of Chemical in Commerce?) Responsibility: Operating Company DEO or designate.
Contact the Manager of Administrative Services in the Department of Safety and Environmental
Health Administration and have the TSCA non-confidential searched for the substance.
If the substance is on the TSCA nonconfidential inventory, it is not new under TSCA definition and a PMN is not required. If the substance in question is not on the nonconfidentiai inventory, the con-fidential inventory must be searched.
To search the confidential inventory, a Bona Fide Intent to Manufacture (BIM) Notice must be submitted to EPA. A copy of the instructions for submitting a BIM can be found in 720.25 of 40 CFR 720. Send a copy of the BIM to the DRM, TSCA for corporate record-keeping purposes.
If EPA reports that the substance is not on the confidential inventory, then the substance is a new substance under TSCA and a PMN is required unless the material is exempt under Section 1 (a) above.
3. What information is required on a PMN submission?
Final rules detailing the PMN requirements can be found in 40 CFR 720. All PMNs must be submitted on EPA Form 7710-25 (4/26/83). Copies of the form and instructions for its use are available from the DRM, TSCA. The required PMN information falls into either the category of General Information or Risk Assessment Data. EPA will accept additional data. In many cases, it is desirable to submit Risk Analysis or other information to assist EPA with their assessment. Since Monsanto performs a Risk Analysis on all new products via Corporate Environmental Protection Guidelines and the EC-201 and 202 procedures, the information is available for this purpose. :
MONSANTO COMPANY
DSW 117635
PR4-1
WATER_PCB-SD0000021430
PREMANUFACTURE NOTIFICATION TO EPA UNDER TSCA - U.S. (continued)
4. What are the details of the PMN procedure?
The PMN process should be integrated into the development scheme of a new project. In most cases, the PMN development will be initiated during the earliest phases of commercialization of a product. The PMN must be submitted to EPA at least 90 days before the product can be manufactured for commercial purposes, including test marketing.
a. How is a PMN initiated? Responsibility: Operating Company DEO or designate.
The Operating Company contact submits an . ER-200 or EC-201 to the Department of Medicine and Health Science (DMHS) if one has not already been submitted (See Monsanto booklet G-2738 for ER-200 and EC-201-202 Procedures).
The Operating Company contact drafts a PMN using the EPA form.
The Operating Company contact calls a scoping meeting. Minimum participants at the meeting are Operating Company contact. Operating Company DEO or designate (if not serving as a contact), member of Corporate Environmental Sciences group or other qualified environmental effects expert (if appropriate), DMHS toxicologist and DRM-TSCA. Copies of PMN drafts, along with an approved ER-200 or EC-201 for the substance are supplied to participants.
At the scoping meeting, decisions are made by the Operating Company contact, as to the scope and detail of optional information to supply. If optional risk analysis is required, assignments are made to DMHS toxicology, industrial hygiene, etc., to complete the necessary sections. A decision is also made as to whether an EC-202 is needed before a PMN submission. Note: It is appropriate at this stage of product development to initiate a Material
. Safety Data Sheet and a TF-837 for label and freight classification.
b. How are PMNs finalized? Responsibility: Operating Company DEO or other designated Operating Company contact.
The Operating Company contact prepares a final draft using input from the scoping meeting as well as follow-up input from DMHS.
The Operating Company contact, together with the patent department reviews the final draft for confidential information and develops appropriate confidentiality claims with substantiation, where necessary.
The final draft is circulated to the participants of the scoping meeting for final review.
The Operating Company contact calls a meeting for final comments/approvals.
c. How are PMNs submitted? Responsibility: DRM, TSCA
After final review/approval, the Operating Company contact forwards the PMN to the DRM, TSCA (Authorized Official), for submission.
The DRM, TSCA will submit the PMN (both confidential and non-confidential as appropriate), using applicable EPA submission requirements.
d. How is EPA follow-up on a PMN handled?
Each PMN will identify a technical contact in addition to an authorized official. The technical. contact will typically be an Operating Company DEO, Commercial Development, or R&D contact.
Phone Contact
All calls from the EPA on technical matters should be handled by the "Technical Contact."
All verbal questions concerning non-confidential inquiries by the EPA may be discussed at the time of call or deferred to obtain an answer if unknown or if unsure as to EPA authority to ask for the information.
Non-confidential oral responses may be followed up with a written response when deemed appropriate by the contact. In all cases the technical contact should write a note to file documenting the conversations, with a copy to the DRM. TSCA.
Confidential inquiries previously discussed with die EPA or claimed confidential in the PMN may be discussed at the discretion of the technical contact.
All other verbal confidential questions will be addressed by written response only.
PR4-2
os** 117636
WATER_PCB-SD0000021431
MInJ PROCEDURE
PREMANUFACTURE NOTIFICATIONS TO EPA UNDER TSCA - U.S. (continued)
Phone Contact (continued)
Uncertain areas of confidentiality will be deferred and handled according to item (5).
(
Verbal response to EPA will be followed up, at the discretion of the technical contact, with a written letter documenting the conversation and clearly indicating areas of confidentiality.
EPA Actions
Responsibility:
The Operating Company DEO or designate will have prime responsibility, with counsel of Environmental Law and the DRM, TSCA.
EPA may extend the review period by an additional 90 days.
EPA may ask for more information under Section 5(e). i.) An order may be issued by EPA. ii.) A consent order may be jointly agreed, to. The consent order can include restriction on manufacture or use in lieu of information generation. (Note: As a rule, consent orders should be signed by linemanagement).
EPA may restrict manufacture or use under Section 5(f).
e. How is Monsanto follow-up on the PMN submission handled? Responsibility: Operating Company DEO or designate.
Monsanto may request EPA to stop the clock on PMN reviews at any time during the review period.
After EPA's review period expires, manufacture can commence at any time, subject to any 5(e) or 5(f) restrictions. A Notice of Commence to Manufacture (NCM) must be submitted to EPA within 30 days of the first manufacture for commercial, purposes. The information to be included in the notice are detailed in 40 CFR 720. Confidential claims must be made again at this time, as appropriate. Send a copy of the NCM to the DRM, TSCA for corporate recordkeeping purposes. Once a NCM is filed with EPA, the PMN substance is placed on the TSCA inventory.
(Approved: Operating Company Directors of Environmental Operations and the Director, Regulatory Management TSCA, October, 1983.)
(Reviewed and Approved: Environmental Safety and Health Committee, October 20, 1987.)
U
MONSANTO COMPANY
DSW 117637
WATER_PCB-SD0000021432
PROCEDURE
OCCUPATIONAL FATAL ACCIDENT REPORTING
In case of a fatal accident, Monsanto's Law Department must be contacted in addition to government, operating company, and corporate reporting requirements.
OSHA regulations require that, within 48 hours after the occurrence of an employment accident which is fatal to one or more employees or which results in hospitalization of five or more employees, the employer of such employee(s) shall report the accident either orally or in writing to the nearest office of the OSHA Area Director. The reporting may bd by telephone or telegraph. The report shall relate the circumstances of the accident, the number of fatalities, and the extent of any injuries.
In such in<fanr^< the following Monsanto guidelines are considered necessary to protect the civil rights of company employees.
In addition to routine Operating Company and Corporate notifications in fatal accidents, either Mary M. Tonkin or Michael E. Gewin (for accidental deaths) or L. William Higley (for deaths from long-term chemical exposure), Monsanto's attorneys for OSHA matters, must be notified immediately.* They will provide prompt necessary legal guidance including, where necessary, sending an attorney to the site for onthe-spot counseling.
In the meantime, OSHA inspectors) should be given access to the site of the accident when the inspector arrives on the premises, without requiring that the inspector secure a warrant for entry. However, neither members of location management nor any wage employee should discuss the accident with the OSHA inspector until advised to do so by the company attorney.
The location manager or his designee will greet the inspector and state that location employees have been asked not to discuss the accident until the company attorney advises them accordingly.
The inspector is to be told that we have been forced to take this posture as a result of the OSHA Procedure for Investigating Criminal/Willful Violations. The inspector will be permitted to inspect the plant, and, of course, should be advised of any chemical hazards and protective measures needed, related or not to the accident.
MONSANTO COMPANY
Location personal will not allow the inspector to view any records or documents at this time, other than the lost-time injury log, OSHA Form 200 and Form 101 or its equivalent, until advised to do so by the company attorney.
If the location is requested to rope off the area of the accident, local discretion should be exercised. The inspector, however, is not authorized to keep plant ' management away from any part of the operation.
If local management believes entry by the inspector must be delayed for a few hours because of exposure, safety, confusion, etc, seek such a recommendation from Ms. Tonkin or Mr. Higley at the time of the initial call to St Louis. '
* Mary M. Tonkin, 314/694-2967 (office), 314/721-8209 (home).
Michael E. Gewin, 314/694-2849 (office), 314/352-2176 (home).
L. William Higley, 314/694-8503 (office); 314/862-1796 (home).
(Approved: Environmental Policy Committee, February 18, 1980.)
(Reviewed and Approved: Environmental, Safety and -- Health Committee, October 20, 1987.)
(Updated for "key contacts, December 16, 1991)
DSW 11763
-PR5-1
WATER PCB-SD0000021433
PROCEDURE
)
TRANSMITTAL OF TOXICOLOGY AND HEALTH-RELATED DATA TO REGULATORY AGENCIES - U.S.
Health-related information should be submitted through the Department of Medicine and Health Sciences.
.4
The various regulatory agencies are continually supplied
4. If the submission includes data on human health
information from toxicology and health-related tests on
effects, it is preferable that the information be
Monsanto products done by or for Monsanto. In order to
submitted to the regulatory agency by the Director
provide consistency in the handling and review of such
of the Department of Medicine and Health
information, as well as to assure proper follOw-through
Sciences.
on commitments to these agencies, the transmittal of such test results will be carried out in accordance with the
5. Agreements with a regulatory agency which
following guidelines:
. commit Monsanto to the future transmittal of toxicology or health-related data must also be
1. All toxicology or health-related data will be reviewed with the Department of Medicine and
reviewed and approved in advance by DMHS; further, DMHS must concur with the feasibility of
Health Sciences (DMHS) prior to submission to
meeting commitment dates. Appropriate records of
any regulatory agency, except for routine
such commitments must be maintained both by the
submissions by Monsanto Agricultural Company
involved operating company and DMHS in order
of test data re-quired under FDFRA. In addition,
to assure future Monsanto compliance with such
V) DMHS will be informed of all such submissions at
the time via the letter of transmittal.
agreements.
6. Any exceptions to the above must be approved by
2. Any such information transmitted must be
the Director of DMHS.
recorded and the copy of the final submission
retained both by DMHS and the involved
operating company.
3. The letter of transmittal for any toxicology or health-related data must include a listing of the materials being transmitted including sufficient bibliographic information for subsequent retrieval of the original data.
(Approved: Environmental Policy Committee, January 17, 1984.)
(Reviewed and Approved: Environmental, Safety and Health Committee, October 20, 1987.)
i
MONSANTO COMPANY
DSW 117639
PRA.l
WATER_PCB-SD0000021434
rui InJ
GUIDEUNE/PROCEDURE
employees, representatives and agents, shall not be liable for and Contractor releases and discharges Monsanto, its subsidiaries, and their respective employees, representatives and agents, from any and all claims, liabilities, actions, suits, judgments, losses, illnesses, injuries, deaths, damages, costs and expenses arising out of, related to , or connected with Monsanto's providing to, or use by, Contractor, its employees, representatives or agents, of the above described items, services, tools, equipment or facilities, (2) Contractor assumes all risk and responsibility therefore, (3) Contractor shall indemnify and save harmless Monsanto, its subsidiaries, and their respective employees, representatives and agents from and against any and all such claims, liabilities, actions, suits, judgments, losses, illnesses, injuries, deaths, damages, costs and expenses and (4) the foregoing shall apply irrespective of any negligence or fault of Monsanto, its subsidiaries, or their respective employees, representatives or agents, whether such negligence orfault is joint, several, sole or otherwise.
) Die items, services, tools, equipment orfacilities are provided by Monsanto on an AS IS, WHEREIS BASIS. MONSANTO MAKES NO WARRANTY OR REPRESENTATION OF ANY KIND, EXPRESS OR IMPUED, WITH RESPECT TO THE ITEMS, SERVICES, TOOLS, EQUIPMENT OR FACILITIES AND MAKES NO WARRANTY OF MERCHANTABILITY OR FITNESS FOR ANY PURPOSE
Contractor agrees to return any items, tools, equipment or facilities in the same, good-working condition as received from Monsanto.
14.2 Should Contractor refuse to agree to the above, the Contractor is not to be pennitted to use Monsanto tools, first aid/medical facilities, equipment, breathing air apparatus, or other services.
(Reviewed and Approved: Manufacturing Management Council, August 6, 1990; Environmental, Safety and Health Committee, September 19, 1990)
)
MONSANTO COMPANY
DSW 11J6Q0 OG-6.7
/lonsanto
OM (H<ne-toction-Pho^)
H. L. Reding - DIR - 4-2106
y:\
sjEct
: :
FEREMCE :
November 27, 1990
Environmental Safety and Health Guidelines
cc.-
) : Distribution List
Attached is a revised issue of the Contractor Health and Safety Guideline/Procedure. This document is part of Monsanto's corporate Environmental, Safety and Health Guidelines and, as such, serves to communicate the intentions and expectations of the corporation. Monsanto has recognized for some time the need for the corporation to act uniformly on environmental, safety and health matters. Collectively, these guidelines serve that purpose.
The changes to the Contractor Safety and Health Guideline were primarily motivated by the corporation's desire for con tinuously improving performance. However, other concurrent developments prompted even broader Revisions, specifically CMA's Code of Management Practice for Process Safety and Monsanto's introduction of a substance abuse policy. Every effort has been made to not only accommodate these require ments but to retain the managerial flexibility present in the original version of the guideline.
The key changes require that the contractor:
1) Have a substance abuse program for employees involved in safety-sensitive work,
2) Include with the submission of the bid relevant information pertaining to their safety record, the training and experience of employees, safe work procedures used, and substance abuse program status, and
3) Hold a review with Monsanto representatives to discuss hazards identified with the job and the precautions to be taken.
Obviously, all Monsanto operations have yet to fully implement
the substance abuse program and not all contractors will be in
a position to meet these new requirements immediately. How
ever, each site is expected to respond in a manner which brings
their facility into compliance in the shortest reasonable time
frame.
-
OSW 117601
WATER_PCB-SD0000021436
2- -
Please remove the prior issue of this guideline/procedure from the ''Other Guidelines" section of the Environmental, Safety and Health Guidelines book and insert this updated version.
attachment
f[l
N. L. Redin<
OSH 117602
WATER PCB-SD0000021437
MInJ
\
GUIDELINE
RESEARCH ANIMAL CARE
Monsanto Company recognizes that animals must be used in research both to determine the effects of
various biologically active materials and the safety of all products. However, it is the stated purpose
of the company that animals be utilized only when necessary and always in a humane and considerate
fashion.
'.
Monsanto encourages and supports efforts to develop safety testing procedures which do not involve animals and will encourage their use and official recognition as and when their scientific validity is established.
.
Research investigators shall abide by the terms of the Animal Welfare Act and shall at all times follow the Guide for the Care and Use of Laboratory Animals as issued by the National Research Council.
A designated officer of the company will each year appoint a committee to be known as the Monsanto Research Animal Committee. This committee will be composed of at least three members and will have at least one representative from each major user group within Monsanto and at least one veterinarian actively engaged in the care of research animals.
It shall be the responsibility of the committee and the Animal Resources Veterinarian to assure full compliance with existing laws and guidelines as they relate to the care and utilization of animals at Monsanto.
Responsibilities of this committee will include but not be
limited to the following:
1
1. Provide for review and approval of all protocols which involve the use.of live animals.
2. review and approve all facilities which house animals for research including new facilities in the planning phase and, .
3. together with the Animal Resources Veterinarian, assure that corrective action is taken if deficiencies
.. or violations occur. It shall further be the responsibility of this committee to file with the United States Department of Agriculture a report of animal usage at the end of each year.
It shall continually be the goal of Monsanto to give high consideration to the well-being of all animals used by .this company.
(Policy approved by the Corporate Administrative Committee, October 6, 1980; revisions approved by the Environmental Policy Committee, March 20, 1984.)
(Reviewed and Approved: Environmental, Safety and Health Committee, October 20, 1987.)
MONSANTO COMPANY
OSW M7603
WATER PCB-SD0000021438
rinuJi PROCEDURE
EMPLOYEE HEALTH AND EXPOSURE COMMUNICATIONS
It is Monsanto's intent to identify hazards of chemical substances and physical agents in the worlqjlace and to communicate such hazards to employees who may be exposed
L Responsibffitici
Identification of health hazards of chemical
substances, physical agents, and biological agents in
the workplace is the joint responsibility of site
managrmenr, the Directors - Environmental
Operations (DEOs) and Corporate Environmental
Safety and Health (ESH). Line management is
responsible for the necessary communications to
and education and training of employees on such
harard<
'.
Europe/Africa Specific: The Director of DMHS Europe/Africa also assumes responsibility for the necessary Communications within Europe/Africa. In Europe, the DEO is represented by the Director, Environmental and Regulatory Affairs. Other countries/regions may specify additional functions who share responsibility.
2 Employee Communication, Education and Training Concerning Ac Hazards of Substances in Ac Workplace
All employees whose work provides potential exposure to a hazardous chemical substance will have ready access to reference material, such as a Material Safety Data Sheet (MSDS), and will receive training in the nature of the hazards and appropriate work practices, protective measures and emergency procedures. Such training will be provided to employees when newly assigned to an area with potentially hazardous exposures and annually thereafter.
3. Employee Access to Medical and Exposure Records
Access to an employee's medical or exposure records (if generated) will be provided within IS
working days after Monsanto receives a request in person or in writing from that employee, or as required by law if more stringent.
In addition to individual medical and exposure records, an employee may have access to general exposure records (such as area samples) for his/her
MONSANTO COMPANY
work area and the individual exposure records (with all identifiers deleted) of other employees in the same work environment. Since much of the data requires interpretation or explanation, the most appropriate physician or nurse should be present during the review of medical records, and the industrial hygienist or industrial hygiene contact should be present during the review of exposure records to provide such interpretation and consultation.
Written requests for medical and exposure records will be kept at the location housing the records.
4. Other Communication of Exposure Information
Employees who participate in individual (personal) industrial hygiene monitoring will be informed of the sampling results.
All employees in an area where ambient air concentrations or physical agents are monitored should be informed of area concentrations, their relationship to relevant federal, state or local permissible exposure limits, Monsanto guidelines and intended corrective action where required.
U.S. Specific: For certain substances, OSHA regulations require written notification to the employee.
5. Communication ofPhysical Examination and Medical Test Data to the Employee
An employee will be informed about results of health evaluations and medical tests. Copies of medical information will be sent to private physicians upon the employee's request and only with written authorization.
U.S. Specific The employee will be informed in writing about results of health evaluations performed for occupational surveillance.
~
DSh 11760**
PR1-1
WATER PCB-SD0000021439
EMPLOYEE HEALTH AND EXPOSURE COMMUNICATIONS (continued)
d. Employee Inquiries
Any employee inquiry about work exposures must be addressed by site management. The location physician, industrial hygienist or other appropriate management representative(s) should meet with the employee and provide a specific response based on the factual information available. The appropriate DEO, Manager, Human Resources and Corporate Environmental, Safety and Health representative should be consulted in any non*routine situation.
Europe/Africa Specific: The Director of DMHS Europe/Africa should be consulted in any non routine situation in Europe/Africa.
7. Communication cf Healih Studies
When employees have been involved in epidemiology or other health studies conducted by or on behalf of Monsanto, an executive summary of the study results prepared by ESH will be communicated in writing to the responsible DEO and site managers. Communications with the employees will be coordinated by the DEO. The DEO may ask ESH and/or Europe Environmental and Regulatory Affairs (ERA) to develop a Communications Document and Dissemination Plan in consultation with plant personnel A decision will be made at that time as to the total population to be included in the communication.
Other studies known to Monsanto which are scientifically sound and which present significant new information concerning the potential hazards of a material to workers should be communicated to employees who have potential exposure to the substance. Where possible, employees should learn of significant potential hazards of materials with which they work from Monsanto, not from outside sources. However, a multitude of epidemiological, animal and other health studies are conducted annually by Monsanto and by others. These studies vary widely in terms of new knowledge provided, scientific validity, conclusiveness of the findings, applicability to humans or the work environment, etc Location management in consultation with the DEO and Corporate Environmental Safety and Health and DMHS Europe/Africa (for Europe/Africa sites) should communicate in writing any applicable, reliable study results.
In determining where the results of a study should
PR1-2
be communicated, factors such as the following should be evaluated:
-- the scientific validity and conclusivcness of the study,
-- whether the study produced new results of significance,
-- the applicability of the study to employees, -- the significance of any potential hazard
identified, and -- the plans for follow-up studies.
When there is a question of whether the results of a study are significant enough to be communicated to appropriate employees corporate-wide, the matter will be referred to the following by any member of concerned management: The Director of Medical and Health Sciences, Industrial Hygiene Director, Corporate Toxicology Director, Epidemiology Director, Medical Director, appropriate DEO and the Assistant General Counsel Environmental The appropriate Directors of Manufacturing, Human Resources and Public Affairs/Relations will also provide consultation. A draft Communication Document and Dissemination Plan will be developed upon request, initially within ESH, to ensure that the study results are properly interpreted and that the communique will be properly reviewed and disseminated to all. operating units and/or plants. The DEO, with support from Corporate Industrial Hygiene and DMHS Europe/Africa (when Europe/Africa sites are involved) will transmit draft statements, announcements and supporting data to the appropriate location management
& Access to Employee Medical or Exposure Records by Designated Representatives
A designated representative with the appropriate written authorization from the employee will be provided access to an employee's medical and exposure records within IS working days of receipt of the authorization. A designated representative is any individual or organization to whom the employee has given written authorization to have access to the employee's medical or exposure records for a specific purpose on a specified occasion.
U.S. Specific OSHA rules require that an employee's recognized or certified Collective bargaining agent will be treated as a designated representative without regard to written employee
-OSW 117605
WATER_PCB-SD0000021440
Ml UL
i 1
PROCEDURE
EMPLOYEE HEALTH AND EXPOSURE COMMUNICATIONS (continued)
8. Access to Employee Medical or Exposure Records by Dcsiffiated Representatives (continued)
authorization with reaped to access to employee exposure records (with all identifiers deleted) and analyses of group medical and exposure records only. Final reports of completed epidemiological studies of unionized employees will be provided to the union involved on specific written request Information on the study results will be provided to all affected employees in a timely manner if this has not been done previously.
The appropriate managers, Human Resources and ESH representatives, (DMHS Europe/Africa when Europe/Africa sites are involved) and the Assistant General Counsel Environmental should be advised
of requests for access to records from a designated representative.
An OSHA inspector who presents a written access ' order approved by the Assistant Secretary of Labor
for OSHA will be given immediate access to records specified by the order. No order is required for access to exposure records. Requests should be reported immediately to the Assistant General Counsel - EnvironmentaL Requests by NIOSH have been supported by the courts but should be cleared by the Assistant General Counsel - Environmental before being granted. Reference should be made to 29 CFR Fart 1910 Access to Employee Exposure and Medical Records, Final Rule 9-29-88.
9. Notification to Employees afRight ofAccess
Each location should make such notification of the
existence, location and right of access to medical
and exposure records a part of its new hire
orientation program and should post or otherwise
inform all employees of this information and right
each year.
10. Employee Health and Exposure Communications Plans
Each manufacturing and laboratory location should have written Employee Health and Exposure
MONSANTO COMPANY
Communications Plans which address such thing* as:
the communication of and training on the hazards of chemical substances and physical agents in the workplace and proper handling methods, protective measures and emergency procedures,
the handling of employee inquiries and expressions of concern about exposures,
the handling of employee and designated representative requests for access to medical and exposure records,
the communication of abnormal physical exam/medical test findings,
the regular communication of the industrial hygiene program and of exposure levels vs. standards,
the identification of materials or other subjects Deeding special communications efforts and plans for development of such programs locally or with the help of DMHS or others, and
notification to employees of their right of access to their medical and exposure records.
1L ESH Responsibilityfor Communication Programs
When its specialized expertise and/or a general communications need makes it appropriate, ESH has a responsibility to develop a Communication Document and Dissemination Plan upon request for new health hazard information. The appropriate DEOs and management at representative plants will be consulted in the development of such plans to make them more suitable and effective for plant use.
Eurooe/Africa Spedfie Europe Environmental and Regulatory Affairs will be responsible for developing a Communication Document and Dissemination Plan which is appropriate for the laws and customs governing handling of employee health and* exposure information in those countries.
OSH 117606
PR1-3
WATER PCB-SDOO00021441
EMPLOYEE HEALTH AND EXPOSURE COMMUNICATIONS (continued)
12 Definitions
Access to Records: Consists of an opportunity to review an employee's medical and exposure records on site, and if requested, receipt of or opportunity to make a copy of the records. Unless otherwise
by law, trade secret informadon may be deleted from the records provided to an employee or designated representative, but they must be so informed that this was done.
Medical Records: Include reports of physical
examinations, medical tests and other medical
informadon on the employee in the Company's
possession.
*
Exposure Records: Include records of an employee's work history and the level of exposure to potentially harmful or toxic substances or agents and analyses of such records.
Epidemiology Studies: Defined as scientific mvesdgadons of potential relationships between workplace exposures and health outcome of Monsanto employees or other occupational populations, as outlined in a study protocol.
(Approved by: Environmental Policy Committee, May 17, 1982.)
(Reviewed and Approved: Environmental, Safety and Health Committee, October 20, 1987.)
(Revised andApproved' DEO Liaison Meeting August 12, 1991.)
m
FR1-4
DSW 1.17607
WATER_PCB-SD000d021442
M
ru
PROCEDURE
TRANSMITTAL TO EPA OF SUBSTANTIAL RISK INFORMATION UNDER TSCA - U.S.
Monsanto procedure for handling the reporting of information to EPA under the 8(e) substantial risk section of the Toxic Substances Control Act (TSCA).
L Abstract ofRequirements - TSCA Section 8(e) requires any person (Company) who manufactures, processes or distributes in commerce a chemical substance or mixture and who obtains information which reasonably supports the conclusion that such substance or mixture presents a substantial risk of injury to health or the environment shall immediately inform the EPA of such information.
2. Who is responsible for reporting?
The requirements of Section 8(e) of the Toxic
Substances Control Act apply to 'any person who
manufactures, processes, or distributes in
commerce.* It is Monsanto's position that the
`person* who engages in the commercial activity is
only the business organization, whether a sole
proprietorship, corporation, partnership, or
.
association.
3. How are 8(e) reporting decisions made7
Monsanto organizations that might receive TSCA 8(e). information will have a designated individual to whom such information shall be communicated. At least annually, the Director of Regulatory Management (DRM) Tone Substances, will publish a list of the designated individuals.
Anyone obtaining information of the type given in
the abstract of requirements and detailed by EPA in
their policy statement On Interpretation and
Enforcement of TSCA 8(e) (43FR 11110, March 16,
1978), should immediately submit such information
to their supervisor.- The supervisor shall
.
immediately relay the information to the location or
department manager, whichever is applicable, who,
in turn, transmits it to the proper designated
individual in the organization. The information is
then transmitted directly to the Director of
Medicine and Health Sciences.
It is imperative that the flow of information through this transmittal chain be rapid. In the event of nonavailability of a member of the communication network at the time information is Erst obtained, such member should be bypassed in the interest of speed.
All individuals involved in submission of substantial risk information to the Director of Medicine and Health Sciences should keep a record of date of receipt and pertinent identifying details.
The Director of Medicine and Health Sciences, Environmental Counsel, DRM - Tone Substances, and the appropriate operating unit Directors) of Environmental Operations will comprise the designated official 8(e) committee to make decisions with respect to information that must be reported to the EPA under Section 8(e) of the Toxic Substances Control Act.
Appropriate Senior Management will be informed of committee decisions.
In the event that a committee decision is not unanimous, the next appropriate level of management shall be consulted, and the matter will be resolved at the highest level, if necessary.
Employees who submit information through Company channels will be notified of action taken by the 8(e) committee together with reasons for such action.
In the event that, after Monsanto has evaluated information and has determined that the item is not reportable under Section 8(e), the Company becomes aware that an employee, as an individual^, subsequently reported the item to the EPA, the Company should review the situation to determine what action, if any, it should take with the EPA-
MONSANTO COMPANY
OSM 117608
WATER_PCB-SD0000021443
TRANSMITTAL TO EPA OF SUBSTANTIAL RISK INFORMATION UNDER TSCA - U.S. (continued)
4. How are employees notified of 8(e) requirements/
All exempt company employees and others so f^cignarcd by their organizational unit (plant nurses, contract physicians, scientists and engineers, etc), within organizations that might receive or have access to TSCA 8(e) information, shall be informed of the provisions of Section 8(e). Annual reminders of 8(e) requirements will be provided to said employees. Records documenting the information communication will be maintained by the DRM Toxic Substances.
(Approved by Vice President, Environmental Policy Staff, April 11, 1986.)
(Reviewed and Approved: Environmental, Safety and Health Committee, October 20, 1987.)
(Revised andApproved by the DEOs and the Vice President, Environmental Policy Staff, May 16, 1991.)
PR2-2
DSW 117609
WATER_PCB-SD0000021444
Monsanto
The Chemical Group 800 N. Lindbergh Boulevard SL Louis. Missouri 63167 Phone: (31 <) 694-1000
October 27, 1992
Dear Monsanto Employee:
A Monsanto procedure is in place to receive and process any interaction that you feel could lead to a conclusion regarding substantial health or environmental risk. This procedure is designed to assist you with appropriate communication of any information of this type and to provide a compliance method for substantial risk reporting under Section 8(e) of the Toxic Substances Control Act (TSCA). A copy of the Monsanto procedure is attached along with a listing of designated individuals in each organization responsible for process implementation.
The kind of information that you should consider for submission into the Monsanto TSCA 8(e) procedure includes:
Human health effects or animal studies that suggest human health effects. Specific attention should be given to cancer, birth defects including reproduction effects, mutagenicity, death or serious or prolonged incapacitation.
Environmental .effects such as widespread and previously unexpected distribution of chemicals in environmental media, pronounced bioaccumulation, and significant changes to species7 interrelationships.
Emergency incidents of environmental contamination that seriously threaten humans or the environment and are not reported under other Federal reporting requirements.
A brief overview of TSCA 8(e) is enclosed. The overview also includes information regarding responsibilities for maintaining allegations, as required under TSCA 8(c). More details regarding the reporting requirements under TSCA 8(c) and 8(e) are available upon request. Please take a few minutes to read the overview.
A Unit of Monsanto Company
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w -2If you have questions, don't hesitate to contact your site TSCA coordinator, your Product Safety Manager, Product Safety Director (J. P. Mieure), J. R. Condray of the Corporate Environmental, Safety and Health or myself. ` Sincerely,
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Garth F. Fort * Director, Environmental Operations GFF/pam Enclosures
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1-1761-1
WATER_PCB-SD0000021446
MONSANTO ESH PROCEDURE PR2-1 REPORTING OF SUBSTANTIAL RISK INFORMATION
DESIGNATED TSCA SECTION
INDIVIDUALS
(YRGANTZATION DMHS ESH - RM/EA CRL THE AGRICULTURAL GROUP THE CHEMICAL GROUP S&EH BSSR
DESIGNATED INDIVIDUAL B. R. FRIEDLANDER J. R. CONDRAY M. J. MONTAGUE R. L. HARNESS G. F. FORT/J. P. MIEURE T. F. EVANS D. J. SCOTT
9/92
' DSW 117612
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PROCEDURE
TRANSMITTAL TO EPA OF SUBSTANTIAL RISK LNFORMATION UNDER TSCA - U.S.
sMeocntisoannotof pthreocTeodxuirce SfuobrshtaanncdelsinCgotnhterorleApocrtti(nTgSCoAf )in. formation to EPA und'r the MeJ, scubst2naal,
1.
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Abstract of Requirements - TSCA Section 8(e) requires any person (Company) who manufactures. processes or distributes in commerce a chemical substance or mixture and who obtains informltion which reasonably supports the conclusion that such substance or mixture presents a substantial risk of injury to health or the environment shall immediately inform the EPAof such information.
'
2. Who is responsible for reporting?
The requirements of Section 8(e) of the Toxic Substances Control Act apply to '`any person who manufactures, processes, or distributes in commerce." It is Monsanto's position that the "person" who k engages in the commercial activity is oniy the f business organization, whether a sole proprietorship, corporation, partnership, or association.
3. How are 8(e) reporting decisions made?
Monsanto organizations that might receive TSCA 8(e) information will have a designated individual to whom such information shall be communicated. At least annually, the Director of Regulatory Management (DRM) - Toxic Substances, will publish a list of the designated individuals.
Anyone obtaining information of the type given in the abstract of requirements and detailed by EPA in their policy statement on Interpretation and Enforcement of TSCA 8(e) (43FR 11110. March 16. 1978), should immediately submit such information to their supervisor. The supervisor shall immediately relay the informanon to the location or department manager, whichever is applicable, who. in turn, transmits it to the proper designated individual in the organization. The information is then transmitted directly to the Director of Medicine and Health .. Sciences.
i
MOMCAKITn COMPANY
It is imperative that the flow of information through this transmittal chain be rapid. In the event of nonavailability of a member of the communication network at the time information is first obtained, such member should be bypassed in the interest of speed.
' All individuals involved in submission of substantial risk information to the Direciorof Medicine and Health Sciences should keep a record of date of receipt and pertinent identifying details.
The Director of Medicine and Health Sciences.
Environmental Counsel. DRM Toxic Substances,
and the appropriate operating unit Directors) of
Environmental Operations will comprise the
designated official 8(e)-commioee to make decisions
with respect to information that must be reported to
the EPA under Section 8(e) of the Toxic Substances
Control Act.
.
Appropriate Senior Management will be informed of committee decisions.
In the event that a committee decision is not unanimous, the next appropriate level of management shall be consulted, and the matter will be resoived at the highest level, if necessary.
Employees who submit information through Company channels will be noaried of action taken by the 8(e) committee togetner with reasons for such action.
In the event that, after Monsanto has evaluated information and has determined that the item is not reportable under Section 8(e). the Company becomes aware that an employee, as an individual, subsequently reported the item to the EPA. the the Company should review the situation to determine what action, if any. it should take with the EPA.
-DSW 117613 PR2-1
:
WATER_PCB-SD0000021448
TSCA SECTIONS 8(c) AND 8(e)
. OVERVIEW
When Congress passed the Toxic Substances Control Act (TSCA) in 1976, it recognized that everyone, including employers, employees and the general public, has a role to play in protecting human health and the environment from the dangers of toxic or hazardous chemicals.
Congress therefore included two sections in TSCA- Sections 8(c) and 8(e) - that place specific obligations on employees of a company to report certain types of - health and environmental information either to the company, or, in certain circumstances, directly to the Environmental Protection Agency. (EPA).
Monsanto has established internal procedures to enable our employees to fulfill these obligations and to simplify the reporting process. It is important that you understand and follow these procedures.
Section 8(c) - Allegations of Significant Adverse Health or Environmental Effects
Section 8(c) was designed to create a historical record that will help Monsanto ' and the EPA identify significant potential risks or environmental threats at an
eariy stage so that they can be controlled before they become serious problems.
Under Monsanto's 8(c) procedure if an employee wishes to internally report any suspicion or allegation that a chemical may pose a health hazard or threat to the environment, the employee may report the matter to the site 8(c) coordinator, who will help document the allegation on a form. The Company then has the responsibility to determine if the allegation should be maintained as required under the law.
If you are told by someone else, such as a fellow employee or a customer, that he or she has been made ill: or even if a neighbor of yours complains that he or she thinks emissions from the plant are, for example, killing fish in the local river or giving him or her headaches, you must transfer the person immediately to the TSCA 8(c) coordinator who is required by law to request that individuals reduce their allegation to writing, sign it and send it to the Company. The Company will process these allegations and maintain them as required by the law. Follow-up actions will be taken by the Company if needed. If you submit an allegation, you will be informed regarding the outcome of the Company's review.
Section 8(e) - Substantial Risk
Section (e) requires employees to report factual information or data which
. supports a conclusion that substantial health or environmental risks may exist
' which the EPA does not already know.
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Unlike Section 8(c), which requires internal reporting and company record keeping of mere allegations or suspicions. Section 8(e) requires internal reporting and review of any factual information that suggests that a Monsanto product presents a "substantial risk" to human health or the environment. If the Company determines that the information reasonably supports a conclusion of a substantial risk, then a prompt submission of this information by the Company will be made to EPA.
;
Types of information that reasonably supports a conclusion of substantial risk include: a serious human health effect such as cancer, birth defects or death: or serious threats to plants, animals .or the environment. Spills or releases of toxic substances which seriously threaten human health or the environment are also "substantial risks".
If you learn of new information that indicates that there could be a "substantial risk", you must ixanediately report this to your supervisor so that the investigation within Monsanto can be undertaken to determine if the information is reportable by the Company to the EPA.
Because the law requires the Company to report the discovery by its employee of new "substantial risk" information to EPA within IS business days, it is critical that you promptly report such information to your supervisor. If he or she is not available, keep going up the line until you find someone who is available. Failure to meet these requirements can result in civil or criminal penalties for both you and the Company.
Don't Take Any Chanrx
Monsanto's sections 8(c) and 8(e) procedures require employees to report both allegatitms and information regarding significant hazards and substantial risk, whether or not it turns out later to be of any importance, or even reportable to the EPA. If in doubt about reporting a specific incident, discuss it with your supervisor. Remember, environmental safety is everyone's responsibility, both as employees and citizens. It's also the law.
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i USZZj
!'CE?.TS F?.OM
TSCA Section 8(e) Reporting Guide
Juna 1991
MQTICT TO ADKIWIgTRATOtt OP 8UB8TMTTTXL RT8M. Any parson who manufactures, [ import:*, ] processes, or distribute In commerce a chemical substance or mixture and who obtains } -information which reasonably supports tha conclusion that such substanca or mixtura prasants a substantial risk of injury to haalth or tha environment shall immediately infora tha [EPA] Adainistrator of such information unlass such parson has actual knowledge that tha Administrator has baan adaquataly informad of such inforaation.
-- faction t(e), Toxic Substances Control lot (197C)
Offica of Toxic Substancas Offica of Pasticidas and Toxic Substancas
U.S. Environmental Protaction Agancy Washington, D.C. 20460
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RgPORTiyq UTTDSR 8ECTTO*
07 TSCA
WET T3 SgCTIOy > (B) RBPORTIffg IXPCRTAKI1
In general, EPA considers Section 8(e) of TSCA to b a critically Important information gathering tool that serves as an "early warning" mechanism for keeping the Agency and others apprised of new-found serious chemical hazards and/or exposures; Section 8(e). .data are extremely valuable input for the hazard identification and risk assessment activities within and outside EPA.
TEAT 18 "STTBSTAirriAL **8*" TXTORXATIOy?
The term "substantial risk" information refers to that information which reasonably support* a conclusion that the subject chemical or mixture presents a substantial risk of injury to health or the environment1; however, such information need not and most typically does not establish conclusively that a substantial risk exists.
In deciding whether information is "substantial risk" information, one must consider 1) the seriousness of the adverse effect, and 2) the fact or probability of the effect's occurrence. In determining TSCA Section 8 (e)-applicability/reportability, these two criteria should be weighted differently depending upon the seriousaess of the effaot or the exteat of the exposure, i.e., the more serious the effect, the less heavily one should weigh actual or potential exposure, and vice versa. For example, in cases where serious effects such as birth defects or cancer (as evidenced by benign and/or malignant tumors) are observed, the mere fact that the implicated chemical is in commerce (including chemicals at the research and development stage) constitutes sufficient evidence of exposure to submit the new-found toxicity data.
EPA has also received numerous Section 8(e) submissions alerting the Agency that chemical substances already known to be capable of caxising serious health and/or environmental effects were detected in significant amounts in environmental media (e.g., soil, surface waters, groundwater, air (including workplace air)) or in products not known previously by the Agency to contain such chemicals. In such cases, the discovery of previously unknown and significant human and/or environmental exposure, when combined with knowledge that the subject chemical is already recognized or suspected as being capable of causing serious adverse health effects (e.g., cancer, birth defects, neurotoxicity) or serious environmental effects (e.g., non-trivial aquatic species toxicity), can provide a sufficient basis to report the new-found exposure data to ?a under Section 8(e) of TSCA.
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The decision-making process for section 8 () -reportability should focus primarily on whether the toxicity or exposure information offers reasonable support for a conclusion of substantial risk under the criteria described above, but ahould not focus at all on whether tha information is conduaiva regarding the risk. A
daciaion to raport information to tha Agancy undar Saction 8(e) should not involva exhaustive health and/or environmental risk aaaaaaaanta of tha aubjact chamical(a). Further, determining raaaonabla aupport for a concluaion of aubetantial risk ahould not includa any avaluation of aithar tha aconoaic or aocial banafita of tha uaa(a) of tha aubjact chemical aubatanca(e). Finally, deter mining vhathar raaaonabla aupport axiata for "substantial risk" is not synonymoum with tha determination of an "unraaaonabla risk" as that tarn ia uaad alaavhara In TSCA.
"Substantial rink" information nuat ba reported to EPA unless tha subject parson has actual knowledge that tha .Agency has bean adequately informed of such information. A detailed discussion of tha types of information about which EPA considers itself to be adequately informed is presented on Page 8 of this
reporting guide under WHAT IHTORXATIow n 9QT eeportabu uhdrs
8ECTI0W 8 (HIT
WHO 18 SUBJECT TO BECTXOH f(E) MFORTIES?
For tha purposes of Section 8(e), the term "person" includes tha following: any natural person, corporation, firm, company, soleproprietorship, joint-venture, partnership, association, or any other business entity, any State or political subdivision of a State, any municipality, any interstate body, and any department or agancy of the Federal Government.
Such "persons" are subject to TSCA Section 8(e) only to tha extant they are engaged in commercial activities involving manufacture, importation, processing or distribution of chamical substances or mixtures under the jurisdiction of TSCA and therefore covered by Section 8(e) of TSCA.
Under Section S(e), there are no exemptions for small businesses, small production or importation volumes, or commercial activities such as manufacture for export only or research and development. However, Section 8(e) does not require a subject person to submit information about a chemical substance or mixture that the person does not manufacture, import, process or distribute commercially. Further, a person who obtains substantial risk information about a chemical or mixture that the person did at one time, but does not any longer, manufacture, import, process or distribute in commerce, is not required to submit the information under Section 8(e).
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m? cmiCALfl ARE SUBJECT TQ BECTIOK 8 (E) RZPORTt^
Chemicals not under TSCA jurisdiction and tharafora not covarad by
Saction 8(e) are discussed in Saction 3 of TSCA and includa:
*
(1) pasticides (as dafinad in tha Padaral Insecticida, Fungicide and Rodanticida Act (FIFRA)) whan manufactured, procassed, or distributed in commerce for use as a pesticide;
(2} tobacco and tobacco products;
(3) source materials, special nuclear materials and byproducts (as defined in the 1954 Atomic Energy Act (AEA) and regulations issued under the AEA);
(4) foods, food additives, drugs, cosmetics, and devices (as defined in the Federal Food, Drug and Cosmetic Act (FFDCA)) vhen manufactured, procassed or distributed in commerce as a food, food additive, drug, cosmetic or device.
Except for those chemicals specifically excluded by definition from TSCA jurisdiction, Section 8(e) of TSCA pertains to all chemical substances and mixtures including but not limited to the following:
(1) research and development (RAD) chemicals (including those intended for use as pesticides prior to application for an Experimental Use Permit (EUF) or a registration under FIFRA);
(2) laboratory reagents;
(3) lov volume chemicals;
(4) polymers;
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(5) chemicals that are manufactured solely for export;
(6) intermediates (including non*isolated intermediates as veil as pesticide intermediates);
(7) catalysts;
(8) byproducts; (9) impurities;
(10) TSCA-covered microorganisms and products therefrom.
Specifically vith regard to "pesticides, a chemical substance that is manufactured, processed or distributed in commerce solely as a pesticide is excluded by Section 3 of TSCA from TSCA regulation. Hovever, a chemical substance which is in the process of research and development (RAO) as a pesticide is subject to TSCA until such time as the manufacturer or importer demonstrates the intent to
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produce a pesticide by submitting to the Agency ta eppiicatioa fcr
an "Experimental Use Permit" (XUP) or registration under ririx.
For further information about this TSCA/FIFRA jurisdictional is*u!
tha raadar is directed to EPA's initial T3CA Chemical Substance
Invantory reporting ragulation (43 FR 64585; December 23, 1977 ; Appendix A Conant 37, 38 and 39) and tha 1986 azandnants' to the
TSCA Saction 5 Premanufacture Notification Rula" (5i fr 15098;
April 22, 1986). Prior to tha FIFRA EUP or ragistration stage,
such RfcD materials ara chemical substances under tha jurisdiction
of TSCA including Saction 8(a).
w
It is important to nota also that vhila soma rulss promulgated by EPA undar other sactionm of TSCA, or undar othar authoritias which ara administarad by EPA, may exempt caxrtain chamical substances and/or mixtures or cartain types of commarcial activitiaa, such axamptions typically apply only to tha rula issued by tha Agancy and not to TSCA in general or Saction 8(a) of TSCA specifically.
TEAT DOF8 TP TERM "0BTAIR8 IMrORXATIQy" KEAE?
Section 8(a) pertains to information that a person possesses or about which tha person knows. Tha Saction 8(a) policy statement explains that an establishment obtains information at tha time any officer or employee who is capable of appreciating tha significance of tha information obtains that information. "Known" information includes that information about which a prudent parson of similar training, job function, etc., could be reasonably expectad to know. Although Saction 8(a) of TSCA does not compel subject parsons to actively search for reportable information or to undertake extra ordinary efforts to retrieve reportable information, negligence or the intentional avoidance of information does not absolve a person of his/her individual Section 8(e) reporting obligations.
Specifically with regard to a public scientific confarenee/meeting,
visually or verbally obtained information from such a meeting is.
subject to Section 8(e) reporting unless the obtained information if captured accurately/adequately in a meeting transcript, abstract or other such written record or document that is to be formally released to the public within a reasonable time frame. Information obtained from a private conference or meeting, however, should be considered for reporting under Saction 8(a) within 15 working days.
WHAT AM TE SOURCES 07 ggCYXQK ? (Rl-tHTOCTMU IgTPHailggl
TSCA Saction 8 (a)-reportable information can come from a variety of sources including, but not limited to draft, interim or final written reports (including study reports, letters, telegrams, telex reports) or verbal reports (received at meetings or by phone) that involve obaervations (including preliminary observations)-from, for example, controlled or uncontrolled;
WATER PCB-SD0000021455
(1) human or animal etudiae/events (including bur nor limited to
studies/events that involve high dcse level* or non-rourin
routes of exposure); or
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(2) environmental svsnts/studiss (including but not limited to
aquatic toxicity studies, bioaccumulation studies, chemical
monitoring studies (supplemented if need be by information
derived fro* computer modeling studies based on actual or
reasonably anticipated chemical exposures and exposure-related
parameters)). It is important to note, however, that modeling
studies, including those based solely on theoretical exposure
data (e.g., "worst-case" scenarios), are
considered by EPA
to be sufficient in and of themselves to meet the Section 8(e)
reporting requirements. Further, environmental or health risk
assessments (including those using ccmputar modeling) based on
either 1) theoretical exposure data, or 2) actual exposure
data submitted on. a mandatory basis under an CPA-administered
statute typically need mot be reported under Section 8(e).
The evidence that offers reasonable support for a conclusion of substantial risk need not be complete nor definitive but should provide a plausible link between 1) an observed serious effect and one or faw chemicals (e.g., in a discrete procesa/operation), or 2) a specific product/activity and a previously unrecognized exposure to a chemical that is known or reasonably anticipated to cause serious adverse health or environmantal affects.
EPA*s March 16, 1978 Section 8(e) policy statement ("Statement of Interpretation and Enforcement Policy; Notification of Substantial Risk" 43 FR 11110) also requires immediate reporting of "Emergency Incidents of Environmental Contamination" (EIEC). An EIEC is an environmantal contamination (accidental or intentional in nature) involving a chemical known to be a sarious human or environmental toxicant and which because of the extant, pattam and amount of the contamination (1) seriously thrsetens humans with cancer, birth dafects, mutation, death or serious or prolonged incapacitation (e.g., neurotoxicologic affects, sarious reproductive system effacts), or (2) seriously threatens non-human organisms with large-scale or ecologically significant population destruction.
TEAT lETORMATTO* II OT ECPORTML1 UTOCR SECTION 8(E)?
Thera are several kinds of information about which the Agency considers itself to be adequately informed already for the purposes of Section 8(e) of TSCA. For example, information that otherwise meets the criteria for Saction 8(a) reporting need not bo submitted if the information meats one or more of the following criteria:
(1) is contained in an EPA study or report.
(2) is published in the open scientific literature. `
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Accachmenc 2
MONSANTO CHEMICAL COMPANY
Rev. 3
ER-200/EC-2Q1/EC-202 IMPLEMENTATION PROCEDURE 07/06/90
Purpose: To describe the actions, including responsibility and timing, to be taken upon approval of EC-201 and EC-202 documents for Monsanto Chemical Company products. Actions to be taken upon approval of ER-200 forms are covered summarily.
Scope: This procedure governs actions for MCC worldwide. In so doing, it addresses MCC coordination with other parts of Monsanto Company that are involved in health, safety, and environmental protection issues (e.g., the Department of Medicine and Health Sciences, Industria1.Hygiene, etc.).
References:
1. Health and Environmental Comoatibi1itv Assessment of Monsanto Products. A Guide to the Use of Department of Medicine and Health Sciences Data Sheet ER--200. EC-201, and EC-202. (G-2738, Rev. S/85).
2. Memo, subj "EC-201/202 Procedure: Europe", 8.R. Friedlander, M.D. to R.L. Harness and M.A.Pierle, December 27, 1989
3. Material Safety Data Sheet (MSDS) System. A Guideline for Format. Content and Preparation. Monsanto Company, July 1989.
4. American National Standards Institute ("ANSI") Standard Z129.1
- 1988
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Procedure:
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ER-200
1.0. Approval of Form ER-200 allows limited (i.e., laboratory scale) sampling for research and development purposes only. As a consequence, only the following actions will be taken by the MCC Manager of Product Safety upon receipt of DMHS approval.
1.1 Notification by the Manager of Product Safety to the submitter (typically, a researcher) of the ER-200 approval (See example memo at Enclosure 1.). This notification shall include any restrictions imposed by DMHS. The Manager of Product Safety shall also provide guidance where applicable as to the next steps being recommended in the product approval process. This may include comments as to timing of submittal of Forms EC-201 and/or EC-202, testing requirements, and Premanufacture Notice considerations. Resp: Manager, Product Safety
1.2 Notification by the Manager of Product Safety to "the site health and safety coordinator (Note: This term is not otherwise defined. It may be that a TSCA Coordinator serves this function. In the event, the intent is to provide notice to that individual
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at a manuficturing or research site with responsibility tor insuring that proper health and safety practices for research samples are followed.) of the approval of Form ER-200, including appropriate safety .guidelines as included in the DMHS approval. Resp: Manager, Product Safety
1.3 Notification by the Manager of Product Safety to the Material Safety Data Sheet Coordinator, allowing issue of a MSDS for Research and Development Purposes. This notification shall include any recommended cautionary language included in the DMHS approval document. Disagreements concerning such language shall be resolved in accordance with procedures established elsewhere for that purpose (Ref. 3) . Resp: Manager, Product Sa-fety
1.4 Forwarding by the MSDS Coordinator of the MSDS for Research and Development Purposes to the submitter, the site industrial hygiene contact,and, if different from the former, the health and safety, contact. This shall be done within one week of notification in 1.3 above. Resp: MSDS Coordinator
1.5 Assessment by the site industrial hygiene contact of industrial hygiene protective measures required. Resp: Site IH Contact
1.6 Communication of hazards and required personal protective measures by the site industrial hygiene contact to employees who may reasonably be expected to be occupationally exposed to the material. Resp: Site IH Contact
1.7 Implementation by the researcher, in coordination with the site industrial hygiene contact, of any industrial hygiene protective measures required. Follow-up responsibilities shall be in accordance with existing site procedures. Resp: Researcher and Site IH Contact
1.8 Recordkeeping, hazard assessment, hazard communication, etc. required to comply with U.S. TSCA or similar ex--U.S. laws shall be the responsibility of the researcher and site TSCA coordinator with assistance from DMHS, Marketing Technical Services ("MTS"), R&D, and Product Safety, respective1y. Resp: Researcher and Site TSCA Coordinator
EC-201
2.0 Approval of a Form EC-201 allows unlimited sampling. Since this may involve significantly increased exposure to humans and the environment and may be viewed as commercial ization _in the context of a Premanufacture or Premarketing Notification, the following requirements must be met.
2.1 Notification by the Manager of Product Safety to the
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submitter (again, typically a researcher) of the approval .'See example memo at Enclosure 2.) as well as of any conditions attached to that approval. The Manager of Product Safety should also include recommendations as to the next step of the approval process. The Manager of Product Safety shall discuss alternate test protocols, as appropriate, with DMHS. For products requiring Premanufacture or Premarketing Notification, this will include DMHS`s prediction of "most likely" and "most probable worst case" testing demands by the competent authorities (e.g.f the U.S. Environmental Protection Agency, Health and Environment Canada, the EEC). The Manager of Product Safety will in cases where such Notification is required also advise other members of the responsible busirtess management unit (e.g., Product Manager, R&D Manager, etc.), presenting a range of test options and recommendations. Resp: Manager, Product Safety
2.2 Notification by the Manager of Product Safety to the site health and safety coordinator of the approval of Form EC-201 and of any conditions pertaining to that approval. Resp: Manager, Product Safety
2.3 Notification by the Manager of Product Safety to the Material Safety Data Sheet Coordinator, allowing initial issue (if no Form ER-200 has been submitted and approved) or revision if necessary of a MSDS for Research and Development Purposes. This notification shall include any recommended cautionary language included in the DMHS approval document. Disagreements concerning such language shall be resolved in accordance with procedures established elsewhere for that purpose (Ref. 3). Resp: Manager, Product Safety
2.4 Forwarding by the MSDS Coordinator of the MSDS for Research and- Development Pruposes to the site industrial hygiene contact within one week of 2.3 above. Resp: MSDS Coordinator
2.5 Assessment by the site industrial hygiene contact of industrial hygiene protective measures required. Resp: Site IH Contact
2.6 Communication of hazards by the site industrial hygiene
contact to employes who may reasonably be expected to be
occupationally exposed to the material.
Resp: Site IH Contact
.
2.7 Implementation by the researcher, in coordination with the
site industrial hygiene contact, of any industrial hygiene
protective measures required. Follow--up responsibilities shall
be in accordance with existing site procedures.
Resp: Researcher and Site IH Contact
-OSW 14.7583
2.8 Communication of environmental concerns by the Manager of Product Safety to the researcher, the appropriate business unit
WATER_PCB-SD0000021459
personnel, and the Manager of Environmental Protection. The Manager of Product Safety shall communicate environmental testing requirements and recommendations' at this time. Resp: Manager, Product Safety
2.9 Development of plant environmental compliance recommendations by the plant environmental contact and Manager of Environmental Protection in conjunction with appropriate business unit personnel. Follow-up responsibi1ities shall be in accordance with existing site procedures. Resp: Manager, Environmental Protection and Site Environmental Contact
2.10 Reaching agreement upon the content and timing of testing
programs by the Manager of Product Safety, Manager of
Environmental Protection^ DMHS, and appropriate business unit
personne1.
Resp: Manager, Product Safety
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2.11 Implementation of testing programs by the Manager of Product Safety and DMHS (In this context as well as throughout, Environmental Sciences Group is included in DMHS.). Resp: Manager, Product Safety
2.12 Communication of the results of testing by DMHS to Tox. Data (formerly Tox. Projects) and the Manager of Product Safety. Evaluation of impact on MSDSs by Tox. Data shall be in accordance with procedures established elsewhere (See Ref. 3). Resp: Manager, Product Safety and Staff Toxicologist
2.13 Communication of the results of testing by the Manager
Product Safety to the MSDS Coordinator for consideration for
inclusion in the MSDS for Research and Development Purposes.
Resp: Manager, Product Safety
of
2.14 Consideration of inclusion of the results of testing by the MSDS Coordinator in consultation with Tox. Data (See 2.12 above.). Resp: MSDS Coordinator
2.15 Communication of the results of environmental testing by the Manager of Product Safety to the Manager of Environmental Protection. Resulting action, if any is required, shall be in accordance with 2.9 above. Resp: Manager, Product Safety_
2.16 Communication of any potential commercial or legal concerns
by the Manager of Product Safety to the appropriate business unit
personnel and Law. Resolution of these concerns shall be in
accordance with the customary practices of that business unit.
However, the Manager of Product Safety is responsible for
notifying the Director of Environmental Operations in the event
that he or she is unsatisfied with the resolution.
Resp: Manager, Product Safety
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2.1" Development of the Premanufactura Notice by the Manager of
Product Safety
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2.17.1 Development of Canadian Notices shall be by the MoCan
Product Safety Coordinator for products solely manufactured and
sold in Canada. If there is U.S. or MESA, manufacture or sale,
the appropriate ^Manager of Product Safety, C.S., MESA, or both,
shall be jointly responsible.
2.17.2 Similarly, Premarketing Notices for products made solely
by and sold solely by MESA shall be the responsibi1ity of the
MESA Manager of Product Safety. If there is U.S. or MoCan
manufacture or sale, the appropriate Product Safety personnel for
the U.S. and/or MoCan*shall be jointly responsible.
2.17.3 In the event of joint responsibility, one of the involved
personnel shall serve as lead. If the involved personnel cannot
reach agreement on that issue, the issue shall be brought to the
attention of U.S., MoCan, and/or.MESA management for resolution.
2.17.4 The responsible Product Safety personnel shall have the assistance of R&D, Manufacturing, DMHS, and others as required. Resp: Manager, Product Safety
2.18 Recordkeeping, hazard assessment, hazard communication,
etc. required to comply with U.S. TSCA or similar ex-U.S. laws
shall be the responsibility of the researcher and site TSCA
coordinator with assistance from DMHS, Marketing Technical
Services ("MTS"), R&D, and Product Safety; and DMHS, Product
Safety, R&D, and MTS, respectively. The site TSCA contact shall
have primary responsibility in this for recordkeeping and hazard
communication. Product Safety and DMHS shall have primary
responsibility for hazard assessment.
--
Resp: As described
EC-202
3.0 Approval of a Form EC-202 allows full commercialization.
Since this will involve significantly increased exposure to
humans and the environment and will be viewed as
commercialization in the context of a Premanufacture or
Premarketing Notification, the following requirements must be
met.
*
3.1 Notification by the Manager of Product Safety to the
submitter (again, typically a researcher) of the approval (See
example memo at Enclosure 3.) .as well as of any conditions
attached to that approval. For products which require
Premanufacture or Premarketing Notification, this will include
notification of the need for filing of Notice of Commencement of
Manufacture in the U.S. and Canadian or EEC equivalent, as
appropriate.
Resp: Manager, Product Safety
' D5W 117585
3.2 Notification by the Manager of Product Safety to the site health and safety coordinator of the approval of Form EC-202 and
WATER_PCB-SD0000021461
or any conditions pertaining to that approval. Resp: Manager, Product Safety 3.3 Notification by the Manager of Product Safety to the Material Safety Data Sheet Coordinator, stating the need for a commercial MSDS. Processing of the commercial MSDS shall be in accordance with procedures established elsewhere (See Ref. 3). This notification shall include any new recommended cautionary language included1in the DMHS approval document. Disagreements concerning such language shall be resolved in accordance with procedures established elsewhere for that purpose (Ref. 3). Resp: Manager, Product Safety
3.4 Forwarding by the.MSDS Coordinator of the MSDS within one
month of 3.3 above in accordance with previously established
distribution schedules. Note that the MSDS Coordinator has prior
notice in the form of a copy of the memo transmitting the Form
EC-202 to DMHS for review (Enclosure 4).
'
Resp: MSDS Coordinator
'
3.5 Development of a commercial label by MCC Distribution.
Conflicts as to label language shall be resolved in accordance
with procedures established elsewhere.
Resp: MCC Labelling
.
3.6 Communication of any newly noted hazards, either human or
environmental, development of compliance and communication
programs, etc. shall proceed in accordance with the
responsibilities outlined for such hazards in 2.1 through 2.18
above.
'
Resp: As described
3:7 Follow-up actions subsequent to EC-202 approval shall be accordance with established existing practices and procedures (e.g., TSCA Sections 8(c) and 8(e); environmental, industrial hygiene, and safety audits, etc.). Resp: As described
in
M.A. Pierle Director, Environmental Operations Monsanto Chemical Company
OSW 117586
WATER_PCB-SD0000021462
GUIDELINE
-3
)
ENVIRONMENTAL, SAFETY AND HEALTH REVIEWS OF CAPITAL PROJECTS
i
Completed Monsanto capital projects will meet Corporate Worldwide Environmental Protection
Guidelines, Corporate Social Responsibility Policies, and will be in compliance with existing and
anticipated government regulatory requirements. Monsanto will, at all levels of the corporation, review
capital projects for environmental safety and health impact prior to, and as a condition of, project
funding approval.
The Senior Vice President, ESH, or his delegate will review those projects requiring approval by the Chief Operating Officer, the Chief Executive Officer or the Board of Directors. A system for reviewing other projects will be administered by the Directors, Environmental Operations, of the operating companies.
The personnel assigned to evaluate a new site for the location of a Monsanto operation will prepare an internal Monsanto Environmental Impact Assessment which addresses potential environmental limitations at the site as a result of the existing socioeconomic and biophysical
conditions. The effects of existing and future government environmental regulations which may apply are also to be considered.
Any exceptions to this guideline must be approved by the Environmental Safety & Health Committee.
(Approved: Environmental Policy Committee, April 21, 1980.)
(Reviewed and Approved: Environmental, Safety and Health Committee, October 20, 1987.)
MONSANTO COMPANY
OSW U 758.7
WATER PCB-SD0000021463
MlnJ
)
GUIDELINE
ENVIRONMENTAL, SAFETY AND HEALTH REVIEW OF DIVESTITURES OR ACQUISITIONS OF PROPERTY AND/OR BUSINESS
Negotiating the acquisition or divestiture of U.S. and ex-U.S. property or business units and the securing of final corporate approval are the primary responsibility of the involved operating company unit. However, corporate staff review of environmental, health and safety factors -- and any attendant liability issues -- are required during the course of such transactions. This review should be arranged through the office of the operating company Director of Environmental Operations, who will, in turn, involve appropriate Environment, Health and Safety staff and Environmental Law personnel and arrange for review by the Vice President, Environmental Policy Staff, and/or the Senior Vice President, Environment, Safety and Health.
(Approved: Environmental, Safety and Health Committee, August 29, 1986.)
(Reviewed and Approved: Environmental, Safety and Health Committee, October 20, 1987.)
MONSANTO COMPANY
OSH 117580
WATER PCB-SD0000021464
GUIDELINE
ENVIRONMENTAL, SAFETY AND HEALTH PROTECTION FOR INVESTMENTS IN WHICH MONSANTO DOES NOT HAVE OPERATING CONTROL
t
Monsanto's six major Worldwide Guidelines apply at all manufacturing sites in the U.S. and ex-U.S. where Monsanto has operating control. For those investments in which Monsanto does not have operating control, we will require, at a minimum, compliance with applicable local laws, regulations and practices. If such applicable rules and practices do not provide safety, health or environmental protection which would be acceptable for Monsanto controlled sites, the company will initiate action to bring about the necessary upgrading.
(Approved: Corporate Administrative Committee, October 6, 1980.) (Revision ApprovedEnvironmental Policy Committee, June, 1985.) . (Reviewed and Approved: Environmental, Safety and Health Committee, October 20, 1987.)
3
MONSANTO COMPANY
JDSW 117589
WATER PCB-SD0000021465
ANNOUNCEMENT
Monsanto
TO: All ESH Worldwide Guideline recipients
On March 20, 1991, the U.S. Supreme Court ruled that the PETAL
PROTECTION POLICY of the Johnson Controls Company is a form of illegal sex discrimination. The effect of the Supreme Court decision is to make femal'e employees responsible for deciding whether they should take jobs that may involve risks to fetal or reproductive health.
Therefore, the MONSANTO guideline, WOKEN EMPLOYED IN AREAS WHICH POSE AN UNACCEPTABLE HAZARD TO THE HUMAN FETUS, is rescinded for all U.S. locations. Monsanto's fetal- and reproductiveprotection policy has covered several substances, but has affected only a small percentage qf job functions at various Monsanto locations. Monsanto will continue to minimize exposures that may be harmful to employees and visitors in all locations - both in the United States and ex-U.S.
Our principal concern continues, to be protecting the health of all Monsanto employees and visitors to our work sites. To this end, a committee chaired by Dr. Jack Baker of Occupational Medicine is evaluating current exposure limits for substances previously associated with the fetal and reproductive protection policy. This committee is made up of representatives from occupational medicine, toxicology, industrial hygiene and related disciplines. Working with Dr. Baker's team are representatives from each operating unit who will work on specific issues and concerns created by the rescission of the fetal protection
guideline.
Findings from the committee's substance evaluation will be
v-
reported to the appropriate work sites within three months. ^ *
Risk-related information will also be communicated at that time.
:
V'
Nicholas L. Reding Corporate Executive Vice President
Environment, Safety, Health & Manufacturing
May 3, 1991
DSW 117590
RD0509-M
WATER PCB-SD0000021466
n_n
LnJ
GUIDELINE
)
WOMEN EMPLOYED IN AREAS WHICH POSE AN UNACCEPTABLE HAZARD TO THE HUMAN FETUS
Women employees of childbearing potential or who are pregnant will not be exposed to work situations which are judged to pose an unacceptable hazard to the human fetus.
The Department of Medicine and Health Sciences will:
Conduct appropriate toxicological tests of Monsanto raw materials, products, intermediates and byproducts.
Review current literature for information on die hazards of chemicals and physical agents used or produced by Monsanto.
Assess safety and health implications and the potential
risks posed by these chemicals and physical agents.
'
Make recommendations to senior management and maintain a record as to work situations which in their judgment pose an unacceptable hazard to the human fetus.
Management of the site(s) involved will take action so "1
that women employees of childbearing potential or who |
are pregnant will not be hired into, be allowed to bid r
into, or continue in job situations which have physical
agents or chemical exposure levels that have been
\
identified by DMHS as posing an unacceptable hazard to j
the human fetus.
S
Where rearrangement of the job situation to avoid exposure to the identified hayard cannot he achieved and an employee has to be transferred out of a job assignment, every effort will be made to protect her job grade level and her seniority.
In instances where the displacement or exclusion of women of childbearing potential adversely affects our EEO goals, efforts will be made to hire or place an equivalent number of women in other departments or areas which do not pose unacceptable hazards to the human fetus.
(Approved: Corporate Administrative Committee, August 7, 1978.)
(Reviewed and Approved: Environmental, Safety and Health Committee, October 20, 1987.)
MONSANTO COMPANY
DSW * U.7594. OG-4
WATER PCB-SD0000021467
fUl
Ini GUIDELINE
SAFE HANDLING OF CARCINOGENS
We will provide safe and healthful working conditions for our employees.
We will comply with all government regulations concerned with exposure to carcinogens. _
Where there is any data which suggest that a chemical to which our employees are exposed is a carcinogen, and such chemical is not subject to government regulations, we will evaluate that data, and based on that evaluation, take the following action:
Where such data establishes the chemical as a human carcinogen, we will take appropriate action to reduce exposure to the lowest reasonable level, unless exposure is already at such a level.
Where such data establishes the chemical as an experimental or suspect carcinogen, we will (individually or jointly with others) initiate study to confirm or
disprove such designation. During such study, exposure will be reduced to and/or minimized at the lowest reasonable level.
If it is concluded that a material cannot be produced or used without jeopardizing the health of employees, its manufacture or use will be discontinued.
(Revised and Approved: Corporate Administrative Committee, October 6, 1980.)
(Reviewed and Approved: Environmental Safety and Health Committee, October 20, 1987.)
MONSANTO COMPANY
OSH 117592
OG-5
WATER PCB-SD0000021468
rLunil GUIDELINE
NONCOMPANY PERSONNEL ON COMPANY SITES
Proper concern for employee health and safety will be required in the execution of contract work per
formed for Monsanto.
*
Monsanto personnel arranging for contract work should observe the following practices.
Work should not begin until a mutually agreeable method of operation has been established.
. Noncompany personnel should conduct themselves so they do not constitute a hazard to Monsanto employees or property.
Apparent violations of the U. S. Occupational Safety and Health Act, other applicable federal, state, and local regulations or accepted industry safe, work practices (CMA, ANSI, NiC, CIA, etc.,) by noncompany personnel should be brought to the attention of their supervisor.
Noncompany personnel must be warned of hazards of Company operations or environments they may encounter so that appropriate precautions can be taken.
Noncompany personnel with special expertise (i.e., those who provide equipment or personnel with particular abilities not readily available on site)
may determine their own safety practices and procedures for performing tasks within their area of expertise commensurate with other Monsanto policies and guidelines. Any such safety practices or procedures which deviate from Monsanto practice or procedure are to be reviewed by the Monsanto contract administrator before implementation.
Entry of Company personnel into the work area of noncompany employees should be minimized and limited to those who need to be involved.
(Approved: Manufacturing Coordination Department, July 1979.)
(Reviewed and Approved: Environmental, Safety and Health Committee, October 20, 1987.)
MONSANTO COMPANY
-OSH 117593
OG-6
WATER PCB-SD0000021469
GUIDELINE/PROCEDURE
CONTRACTOR HEALTH AND SAFETY
Proper concern for employee health and safety will be required in the execution of contract work performed for Monsanto.
SCOPE.
DEFINITIONS
This Contractor Health and Safety Guideline sets forth safety and occupational health guidelines applicable to Contractors performing services on Monsanto Company property where, in the judgment of Monsanto site management, there may exist the potential for personal injury or property damage or for significant safety or health issues to arise. Services administered either by individual sites or by Monsanto Engineering groups are covered. Recognizing that these guidelines may not be appropriate in all cases, judgments may be required by the individual sites as to implementation and application. These judgments are to be made taking into account the objective of this guideline that proper concern be given to Monsanto and contractor employee health and safety in the execution of contract work performed for Monsanto. Substantial departure from these guidelines ' should be approved in advance by the appropriate manufacturing director and, as appropriate, the Department of Medicine and Health Sciences (DMHS). This guideline applies to Monsanto U.S. sites.
OBJECTIVE
All services performed by Contractors on Monsanto sites are to be covered by written contracts. Normally the Contractor is to be made aware of the requirements of this guideline before bidding, the costs agreed upon before contracting the work, and the appropriate requirements incorporated into the written contract or otherwise appropriately documented in consultation with the Purchasing and Law Departments.
In accordance with the objective-of providing for Monsanto and Contractor employee safety and health in the execution of contract work, Monsanto will utilize Contractors who: have demonstrated a high degree of compliance with workplace laws/standards, policies and practices; have a history of good health and safety performance; maintain adequate insurance coverage; and, if involved in safety sensitive work, have a . substance abuse program reasonably equivalent to Monsanto's. Monsanto will take into account the nature " ` of the services, the availability of Contractors, and other relevant considerations.
MONSANTO COMPANY
Contractor A person (other than employee of Monsanto), firm or corporation engaged by Monsanto to provide a service on a Monsanto site.
Contract The writing which contains the agreement of Monsanto and the Contractor with the agreed upon terms and conditions and which serves as proof of their . respective obligations. Contracts are to be signed by authorized representatives of Contractor and Monsanto. Contracts are to be on forms previously approved by the Purchasing and Law Departments for that use (c.g., Master Maintenance Agreement (Form G-2536], Short Form Contract (G-615], etc). Plant purchase order forms may not be utilized for contracts which require on-site Contractor employees unless approved by the Law Department. When approved existing contract forms are not appropriate, the Purchasing and/or Law Departments are to be contacted for assistance.
Monsanto Representative The employee designated by site management to represent Monsanto with respect to the services being performed pursuant to the particular Contract. For Engineering awarded Contracts, this will normally be a site construction superintendent/ supervisor.
RESPONSIBILITIES
While contractors are responsible for assuring healthful and safe operations, work on a Monsanto site may involve unique or site specific health and safety issues as to which this guideline is directed. The manager of each site is responsible for the implementation of this guideline.
CONSIDERATIONS
In furtherance of the objective that Contractors provide a healthful and safe operation at Monsanto locations, the following is to be considered and implemented, when deemed applicable to the service being provided.
OSW I17594
OG-6.1
t WATER PCB-SD0000021470
. 1.0 COORDINATION
The Monsanto Representative is to: 1.1 Coordinate Contractor activity on the site.
12 Be familiar with the Contracts and obtain
Purchasing and Law Department review and
approval as appropriate.
13 In the letting of bids, assure those jobs requiring a functioning substance abuse program are so
identified.
L4 Where appropriate, assure that the submission of bids from potential contractors is accompanied
bT- . The OSHA 200 log summary form for at least
the three most recent years. An evaluation of skill requirements for the
job bid. A tentative listing of the contractor's
employees likely to be assigned to the job together with their training (including . apprentice programs), work history and any other special qualifications. . A listing of written contractor safe work practices/procedures including the substance abuse program. For those contractor employees who will be designated as performing safety critical jobs, the latest date of drug screening and confirmation of acceptable test results.
L5 Review with the contractor his planned approach to the job including those risks he has identified, precautions to be taken, and areas of intended use of his as well as Monsanto procedures.
1.6 Explain to Contractors any unique or site specific safety or health hazards and precautionary measures associated with the services (Orientation).
L7 Apprise Contractor of its responsibilities and restrictions while on sito-to include a mutual exchange of health and safety information, for example Material Safety Data Sheets (MSDSs), as required under the OSHA Hazard Communication Standard.13 * * * *
13 Follow contract services with the objective of having the Contractor minimize potential hazards to both Monsanto and Contractor employees, and to property, which may arise during Contractor services.
OC-6.2
1.9 Conduct in consultation with health and safety professionals a final health and safety evaluation before the job is accepted as completed.
2.0 PRACTICES AND PROCEDURES
2.1 Unique or site specific work hazards involved with the services (of which Monsanto is aware but with which the Contractor may not be familiar) and expected performance relating to such hazards are to be communicated to and reviewed with the prospective Contractor(s) prior to submission of bids. The following items are to be considered and addressed when applicable:
Contractor Safety/Health Orientation Respiratory Protection Hazard Communication Hearing Protection Personal Protective Equipment and Clothing Supervision of Contractor Employees Substance Abuse Policy Hygiene Facilities and Practices Exposure Monitoring Medical Sendees Biological Health Monitoring Injury Reporting ' Use of Plant Permit Systems Site Work Practices Emergency Response and Plant Evacuation Tie-in to Monsanto Equipment Environmental Control Procedures Waste Disposal
(. '
22 Contractors, at a minimum, are to be made aware of and required to comply with proper plant procedures for securing permits involving hot work, tank or other enclosed space entry; breaking into pipelines, lock-out, etc. Permits are to be coordinated through the Monsanto Representative.
23 For confined space entry permits, Monsanto will execute the permit and provide required testing prior to the beginning of contracted work. In case of hot work permits, Monsanto will execute the permit, inspect the area and provide required testing. Agreement on whose responsibility it is to provide a qualified fire watch must be made in writing prior to the beginning of contracted work.
DSW 1-17595
WATER PCB-SD0000021471
rui
Ini
GUIDELINE/PROCEDURE
3.0 ORIENTATION - TRAINING
3.1 Each location is to maintain a general Contractor health and safety qrientation program to convey Monsanto's commitment to health and safety, Contractor general obligations, and plant rules/procedures. The following topics are to be included and addressed when applicable:
General Plant Policies Hazard Communication Hearing Protection Site Safety and Housekeeping Practices Basic Protective Equipment Usage Personal Hygiene Practices Site Emergency Plan Respiratory Protection
.
32 All Contractor employees whose work may
involve unique or site specific health or safety
' hazards will upon first entry to the site and prior
to beginning work in the field be presented
supplemental information pertaining to:
'
Material Safety Data Sheets (MSDSs) for Monsanto hazardous chemicals to which Contractor employees may be potentially exposed;
Known safety and health hazards unique or specific to operating areas in which Contractor personnel will work;
Requirements for any special protective clothing, equipment, or other measures specific to the chemicals involved; and
Other basic orientation information, as appropriate, to operating areas in which contractor employees will work.33
33 The Monsanto Representative, working with the Contractor, Engineering Construction Manager (as appropriate) and site health and safety staff, shall coordinate the orientation sessions. A record of the date, information presented, who conducted the training, and a signed list of attendees will be retained in permanent files maintained by the site.
4.0 SUPERVISION
4.1 In all Contractor services on a Monsanto site, the Contractor is responsible for providing safe
MONSANTO COMPANY
operations, and for the health and safety of its employees.
42 Monsanto will not usually undertake direct supervision of Contractor employees. The Monsanto representative will relate to the Contractor and its employees through the Contractor supervisor in charge at the site. Contractors are to have a competent, responsible supervisor in charge at the site at all times during which its employees or those of its subcontractors are present. However, it is recognized that there may be situations in which it would be impractical for the Contractor to provide full-time,'on-site supervision. Exceptions to the foregoing are to
. be first approved by the Site Manager or his designee.
43 In some instances, a single individual {e.g., a specialized service repair person) who is employed by an outside agency may come onto a site to perform expert service. The Monsanto Representative is to determine that this individual is generally competent to perform the work without supervision.
4.4 In those instances where a Contractor employee has no on-site Contractor supervision, the Monsanto Representative is to proride for appropriate implementation of this guideline. In all other cases, the Contractor is to provide for implementation of this guideline as incorporated in the Contract or otherwise communicated to the Contractor.
5.0 OVERSIGHT
5.1 Contractor operations are to be periodically reviewed by the Monsanto Representative in consultation with health and safety professionals as a further check that the Contractor is complying with applicable health and safety laws, rules and regulations and with contractual requirements and is not endangering personnel and property.
52 If significant non-compliance is observed, the related work is to be immediately suspended and resumed only when compliance with requirements is assured. Contractors are to be advised of all non-compliance matters observed
OSW 1175.96
OG-6.3
WATER PCB-SD0000021472
by the Monsanto Representative and is to be required to bring its operations into compliance promptly.
6.0 PERSONAL PROTECTIVE EQUIPMENT
6.1 The Contractor is to be notified prior to beginning work of the minimum requirements for personal protective equipment such as special work clothing, goggles, gloves, or full body protection.
62 The Contractor is to furnish and require the use and wearing of proper personal protective equipment by its employees.
63 If a Contractor does not have the specified equipment, the task is to be delayed until such equipment is provided by Contractor.
6.4 Persona] protective equipment, including special clothing, are not to be supplied by Monsanto unless dictated by an emergency. (See Section 14.0 for indemnification requirements.)
7.0 RESPIRATORY PROTECTIVE DEVICES
7.1 Use of respiratory protective devices requires a program for proper selection, fitting, training, cleaning and disinfection, storage, inspection and repair, surveillance, periodic evaluation, medical approval, and the use of National Institute of Occupational Safety and Health (NIOSH) approved equipment
12 Contractors are to require each of their employees who will be expected to wear a respirator as part of his/her job to be medically evaluated for approval, properly fitted, and trained in its use prior to beginning work.
13 Documentation of the medical approval to wear a respirator is to be provided by die Contractor to Monsanto for review by the location Medical Services. Where location Medical Services do not exist, documentation -of medical approval is to be submitted to DMHS for review.
Positive pressure self-contained respiratory protective devices designed and used for the sole' purpose of emergency escape do not require medical approval and fitting. These respirators do, however, require training in their application and use.
7.4 Contractors are to be responsible for properly fitting and training its employees. In extenuating
OG-6.4
circumstances, if the Contractor is not able to properly fit and train its employees, Monsanto may, upon written request, consider assisting the Contractor in providing such services. (See Section 14.0 for indemnification requirements.)
7J Contractors are to furnish the proper respiratory protective devices to its employees and to assure that such devices arc used in conformity with applicable laws and regulations.
7.6 In the event that Contractor's employees have not been fit-tested and respiratory protection is necessary, only positive pressure, supplied air equipment is to be used.
7.7 Contractors are to adhere to'the location policy regarding facial hair in the sealing area of respirators.
7.8 Supplied breathing air for respirator usage is to be provided by the Contractor unless dictated by an emergency. Monsanto may, upon written request, consider furnishing breathing air. (See Section 14.0 for indemnification requirements.)
7.9 The Contractor is to test all breathing air
sources for oxygen content, and insure that the
breathing air is certified as meeting the
.
specifications for Grade D air as described in
the Compressed Gas Association Commodity
Specification G-7.1-1973 prior to use, whether
Monsanto or Contractor supplied.
7.10 Monsanto is to retain the right to test at its discretion all supplied breathing air provided by Contractor.
8.0 MEDICAL SERVICES
The listing below includes chemical/physical
agents and situations for which occupational
health surveillance is presently required. This
listing could be changed periodically as
appropriate by DMHS. This surveillance may
be required by regulation and therefore legally
mandated. In addition, there are exposures for
which no legally enacted standard mandates
surveillance, but for which Monsanto requires
periodic health evaluation. Occupational health
surveillance is targeted to specific at-risk groups
as defined by workplace assignment, known
exposure history, and/or workplace monitoring .
data and conducted by performing certain
^
specific health examinations to include the
following:
OSW 117597
WATER PCB-SD0000021473
LMnJ GUIDELINE/PROCEDURE
ACRYLONITRILE FORMALDEHYDE KETHEMOCLOEIN FORMERS
ASBESTOS
HAZARDOUS SUBSTANCE EMERGENCY RESPONSE
PAB
BENZENE
HEARINC PROTECTION REQUIRED
.PHOSPHORUS
CADMIUM
RADIATION
DMAC
LEAD
RESPIRATORY PROTECTION REQUIRED
DMF
MERCURY
Pre-placement health examinations are to be provided for Contractor employees who are employed in jobs for which Monsanto required/legally mandated health examinations would be performed for its full-time employees (if they were to perform the job) and who:
Are or may be potentially exposed at or above the action level (/.., one-half the 8-hour timeweighted average permissible exposure limit or Monsanto workplace exposure guideline) to a chemical/physical agent and situations as identified above;
AND > Are anticipated to work in a designated exposure
area(s) for 30 or more consecutive work days or . where non-consecutive work periods may result in
sufficient cumulative work exposure to warrant evaluation. Such work evaluations wall be conducted by Monsanto Industrial Hygiene in consultation with Occupational Medicine (DMHS) as to what constitutes sufficient cumulative work exposure;
' OR Regardless of work duration, are assigned to a job for which Industrial Hygiene, in consultation with Occupational Medicine, determines sufficient potential exposure to require health examinations.
. When there is any question as to whether or not the job assignment requires special health surveillance or any question as to the specifics of the health examination. Occupational Medicine, DMHS is to be consulted and is the final authority.
Section 8.0 will not normally apply to Construction Contractors unless the service performed is directly associated with an active chemical processing area.
Section 8.0 is not intended to apply to potential ) exposures which might result from possible ' catastrophic events not reasonably foreseeable.
MONSANTO COMPANY
8.1 Specifications for health examinations and provisions for medical services are to be designated in the contract with the providing Contractor or otherwise appropriately communicated to the Contractor.
8.2 Where 'baseline* medical data on Contractor employees are required prior to working in an ' area, sufficient lead time for collection and analysis of samples is to be required in scheduling work.
83 The examinations are to be performed by qualified medical professionals. Examinations may be performed by an outside physiaan(s), identified by the Contractor, who meets the approval of Monsanto.
8.4 Surveillance health examinations for Contractor employees are to follow as closely as possible the examinations as defined for Monsanto employees.
8.5 In the event a specific health examination procedure has not been established. Occupational Medicine (DMHS) is to be consulted.
8.6 Periodic and termination physicals for Contractor employees are to be in accordance with the same frequency/timing practices provided for Monsanto employees similarly situated.
8.7 Maintenance and storage of medical record information on Contractor employees will be at the discretion of the location and will follow the same policies regarding confidentiality and retention as for Monsanto employees. In all cases whether the examination is performed on or off site, a copy is to be accessible to Monsanto medical personnel or be maintained by Monsanto in the same area as the medical records for that site are maintained. Where feasible, Monsanto forms are to be used.
83 Contractors are to assure that medical services are available for contract employees in the event of injury/illness. Where the severity of the injury dictates immediate attention on-site, Monsanto may provide first aid treatment to the extent necessary to stabilize the condition of
OSH I17598
*s
WATER PCB-SD0000021474
MCHAa.A.P6?-
Vfe* PrMdait
Monsanto
Monsanto Company 800 N. Undberati Bodevard St. Louis. Missouri 63167
Pt^wiaH>6`iH IQffl
November 11, 1992
To Our Employees: . ....1 _________ ____ ___
_ _____ . _ _________ :___ ____ ____
Monsanto Company is dedicated to ensuring the safety of our employees, customers, communities and the environment This is the commitment of the Monsanto Pledge, which serves as the umbrella for our overall environmental, safety and health program.
In support of this commitment, we have developed the "Monsanto Pledge Guidelines." These new guidelines replace ourEnyironinental, Safety and Health Guidelines. They set forth the management, expectations for environmental, safety and health performance, and they describe key results against
which progress will be measured.
The Monsanto Pledge Guidelines update our Environmental, Safety and Health Guidelines, and incorporate Responsible Care, the continuous improvement initiative created by the chemical industry worldwide.
~"~Thencw guidelines have been approved-by-the-Envtronmental Policy Committee. ConfonnaflcgL
"with the spirit 61 Iflft gUiqeiiUffl. 1U1UI U[ ' -
"
Mpeetcri in tailoring the guidelines for sperifir operating units.
Please incorporate your existing plans and programs as appropriate to meet the Pledge Guidelines and add any specific programs or requirements that reflect special needs of your business.
To fulfill the Monsanto Pledge, we must engineer change and add value to our businesses. In this way, we can build a competitive advantage to sustain our leadership position in environmental, safety and health improvements.
This Monsanto Pledge Guidelines book should be treated as "company confidential." The section entitled "Introduction," pages i - iii, contains a summary of the Pledge Guidelines and can be used in external discussions.
Sincerely,
Michael A. Pierle
USw 107930
WATER PCB-SD0000021475
TABLE OF CONTENTS
I. INTRODUCTION
II. THE
III. MONSANTO PLEDGE GUIDELINES
1. Pollution Prevention
2. Employee And Community Safety And Health
3. Process Safety And Emergency Response
-------4. Product Stewardship -
------------- --------- --------
5. Chemical Distribution
................ .......... ...........................................
------ 6. Groundwater And Soil Quality ..... . ... .... . ... ......... _. ..____ _
7. Outside Processors
8. Community Awareness At Manufacturing Sites
IV. OTHER GinDELINES --'
- '"
~
1. Environmental. Safety And Health Reviews Of Capital Projects
2. Environmental, Safety And Health Reviews Of Divestitures Or Acquisitions Of Property And/Or Businesses
3. Environmental. Safety And Health Protection For Investments Over Which The
Company Does Nor Have Operating Control - ...... -
.................
-- 4, RcprOdUCtivrBa7arrU *n TVu Wnrlcplar*
...* 1 2 3 4 5 6
5. Sdic Handling OfCaiLluugeiis "
..... '
6. Contractor/Guest Environmental. Safety And Health
1
'
7. Use Of Animals In Research Facilities
8. Ozone-Depleting Chemicals (CFCs) 9. Environmental, Safety And Health Compliance Auditing
V.PROCEDURES
1. Employee Health And Exposure Communications 2. Transmittal To The United States Environmental Protection Agency Of Substantia]
Risk Information Under The Toxic Substances Control Act 3. Recording Allegations Of Significant Adverse Reactions Under The Toxic
Substances Control Act 4. Premanufacture Notification To The United States Environmental Protection
Agency Under The Toxic Substances Control Act 5. Occupational Fatal Accident Reporting 6. Transmittal Of Toxicology And Health-Related Data To United States Regulatory Agencies
VI. REFERENCES Appropriate Responsible Care Program Or Industry initiative
OSW 10 7934.
WATER PCB-SD0000021476
INTRODUCTION
Monsanto's Environmental, Safety and Health Program - The Monsanto Pledge
- MfwcffntnCnmpamis dedicated to ensuringthe safety, ofJiur.employeesK customers,communities andjhe 5 eriviTo^entr ftirbugK theMonsanto Pledge,we have comminedpubliety topursue a course of --
environmental stewardship - one that goes beyond what is required by the law.
I. THE MONSANTO PLEDGE ..............
.................. .......
.........
Each of the company's environmental programs and commitments is embodied by the seven-point Monsanto
Pledge. Announced in 1990 by Monsanto's chairman, Richard J. Mahoney, the Pledge represents Monsanto's
environmental commitment to sustainable development
............ ' -------
- ....
The Monsanto Pledge
It is our pledge to: reduce all toxic and hazardous releases and emissions,
working toward an ultimate goal of zero effect; ensure no Monsanto operation poses any undue risk to
our employees and our communities; work to achieve sustainable agriculture through new
<eehnologv-ndgraciiccsi
keep our plants open to our communities and involve the community in plant operations;
manage all corporate real estate, including plant sites, to benefit nature; and
search worldwide for technology to reduce and eliminate waste from our operations, with the top priority being not making waste in the first place.
At the core of the Pledge is our belief that the public grants us the right to operate every day - and every day, we must work to earn that right. The Pledge recognizes that outstanding environmental, safety and health performance isn't a cost of doing business, but is integral to our business success. It assumes that compliance with the law and our internal guidelines is basic, wherever we do business. But the environmentalism embodied in the Pledge is far more than compliance.
The Monsanto Pledge sets the overall direction of the company's environmental, safety and health program. Specific guidelines detail our efforts to achieve the Pledge.
OSW 107932
I
WATER PCB-SD0000021477
II. MONSANTO PLEDGE GUIDELINES
All of Monsanto's operations worldwide observe eight Monsanto Pledge Guidelines that help ensure that our products and operations fully protect human health, safety and the environment -- while meeting or exceeding existing regulations.
1. Pollution Prevention -- The company will work toward the ultimate goal of ensuring zero effect attributable to waste in all media. It will research, design and operate its facilities to minimize the generation of process and - nonprocess waste and the potential effect of chemical releases to theenvironment. Frir"waste and releases that remain, the company will comply with regulations, while minimizing environmental threat and long-term
liability.
2. Employee and Community Safety and Health -The company will provide a healthful and safe environment for its employees, site visitors, contractors and neighbors. It will evaluate employee health status, determine and monitor workplace factors affecting employee safety and health, and comply with both the company's workplace exposure guidelines and governmental safety and health regulations. It will review major capital projects to protect the health of its people at work and that of people in the community.
3. Process Safety and Emergency Response - The company will research, develop, design and operate processes in a manner that protects the health and safety of employees, site visitors, contractors and neighbors. Beyond compliance with appropriate governmental regulations, the company will apply such standards and programs as necessary to manage operational risks at a level that ensures its continuing right to operate. All - company sites will complement this effort with strategies to mitigate risk in the event of an incident .including site emergency response and support of comparable efforts within the community.
4. Product Stewardship - The company will research, develop, design, assess, manufacture, market and dispose of its products so that they meet societal needs and do not pose undue risk to human health or to the environment during all stages of their life cycles. The company will work with product stake holders (suppliers, employees, distributors, customers, consumers and disposers) to understand and reduce risks associated with the life cycle of the company's products. ..............
gifTJlstrlbutlou - Thectympany wn reaucj distributors, contractors, aistnm^' employees, and tEe envirot
6. Groundwater and Soil Quality - The company will design and operate facilities to protect groundwater and soil quality. The company will assess groundwater and soil quality at its facilities and pursue remedies for releases that threaten health or the environment. The company will address on-site and off-site contamination of groundwater and soil attributable to its operating and waste practices to ensure protection of health and the environment
7. Outside Processors - To support its operations, the company will select outside processors that will operate
with concern for worker safety, regulatory compliance, community protection and protection of the
environment
*
8. Community Awareness at Manufacturing Sites -- The company will foster its employees' and the public's right-to-know through a commitment to openness, involvement and community dialogue. The company will be responsive to questions and concerns about human safety, health and the environment at its manufacturing sites.
Included in these guidelines are Monsanto's voluntary programs to prevent pollution and improve safety performance. Also included are specific elements of the Responsible Care initiative.
DSM 107933
It
WATER_PCB-SD0000021478
III. RESPONSIBLE CARE
.
Monsanto actively participates in the chemical industry's Responsible Care initiative, the most ambitious initiative on environmental, safety and health issues ever undertaken by a manufacturing industry. Responsible Care is woven into the very fabric of Monsanto's commitment to environmental, safety and health protection worldwide. It is an important tool to help the company fulfill the Monsanto Pledge.
Six R^ponsible Care codes of management practice are included in the Monsanto Pledge Guidelines:
1. Community Awareness and Emergency Response - to bring company operations and local communities together through communication and cooperative emergency planning.
2. Distribution - to make the transportation of chemicals safer, regardless of the carrier or mode of shipment.
3. Pollution Prevention - to decrease the amount of pollution and hazardous waste generated by
manufacturing operations.
*
4. Process Safety - to prevent fires, explosions or chemical releases from manufacturing plants and processes.
5. Employee Health and Safety - to improve continuously the protection of employees, contract workers and visitors at company sites.
-- 6. Product Stewardship ~ to reduce the risks to health, safety and environment at every stage of the
company's products, from proposal to disposal.
'" ---- --- -- ...... --.. ..
Responsible Care is an important part of the operation of every Monsanto facility. It is a vital part of our effort to earn the public's trust and the privilege of continued operation.
By weaving Responsible Care elements into its environmental, safety and health initiatives, Monsanto is forming -the solid foundation it needs to ensure the welfare of its employees, customers, communities and the environment.
Note: Responsible Core is a registered service mark ofthe Canadian Chemical Producers Association and the U.S. Chemical Manufacturers Association, and is an initiative that is being adopted increasingly in countries around the world.
OSM 107934
Iff
WATER_PCB-SD0000021479
0%ie Monsanto
It is our pledge to:
<& reduce all toxic and hazardous releases and emissions, working toward an ultimate goal ofzero effect;
<9* ensure no Monsanto operation poses any undue risk to our employees and our communities;
<3t worktoachieite sustainable agriculture through new
technology and practices;
" ...............
<3t ensure groundwater safety;
<9* keep our pbnts open to our communities and involve the
__ _____________
t-- jJiiTiiiTi;r all frrpcrn^oni ocintp to benefit nature; and
plant affo,
<3 search worldwidefor technology to reduce and eliminate waste from our operations, mth the top priority being not making it in thefirst place.
Monsanto
January 1990
53
Chaiirfian and Chief Exe :ive Officer Monsanto Company
OSW 107935
WATER PCB-SD0000021480
MONSANTO PLEDGE GUIDELINE
#1
The company will work toward the ultimate goal ofensuring zero effect attributable to waste in all
media. It will research, design and operate its facilities to minimize the generation ofprocess and
nonprocess waste and the potential effect ofchemical releases to the environment. For waste and
releases that remain, the company will comply with regulations, while minimizing environmental
threat and long-term liability. ..... .... ..........
........
-
............
KEY RESULTS...............
Reduce by 90 percent the company's 1987 level of
worldwide air emissions of chemicals named by the
United States Environmental Protection Agency..-~r.
(USEPA) under Title III of the Superfund
-
Amendments and Reauthorization Act (SARA Section
313) and chemicals of local concern outside the
United States by the end of 1992.
Reduce by 70 percent the company's worldwide SARA Section 313, European Community Priority Pollutant List (EC 129) and carbon monoxide
Discontinue the deep-well injection of Resource Conservation and Recovery Act (RCRA) hazardous waste streams and SARA Section 313 toxic chemicals by the end of 1999.
PROGRAM
1.1 Process Waste
The operating units will integrate into their release reduc tion plans the corporate goal of reducing all toxic and hazardous releases and emission to all media, working toward an ultimate goal of zero effect For reducing releases from processes, the order of preference is source reduction, followed by reuse, recycling or co-product sale, and finally by incineration or other treatment to reduce the volume and/or toxicity of pollutant streams.
The development and use of technologies that improve competitive positions will be emphasized.
The operating units will integrate into their release-
Reduce by 90 percent the company's 1987 level of worldwide air emissions of SARA Section 313 chemicals and chemicals of local concern outside the United States by the end of 1992.
Reduce by 70 percent the company's worldwide
tiglpntieag'aardfpa - hy end af 190S. The January 1990 SARA 313 and--
- EC 129 lists plus carbon monoxide apply through the end of the `multimedia release reduction program. "
An effect-based release reduction target will be established every five years beginning in 1995, working toward an ultimate goal of zero effect By the end of 1993. a method and process for an effect-based reduction program for toxic chemicals will be developed.
1.2 Nonprocess Waste Each facility will maintain an inventory of all nonprocess sources of waste generation, including power generation, office and maintenance operations, general warehouse trash, packaging/shipping materials and similar sources.
13 Underground Well (Deep-well) Injection
MONSANTO COMPANY
0 S W 107 93 6
MPG 1. Page 1 of 3 Company Confidential
WATER PCB-SD0000021481
The company will discontinue deep-well injection of RCRA hazardous waste streams by the end of 1999. It will also apply best feasible technology to virtually eliminate the deep-well injection of SARA 313 chemicals. The company's name will not appear on the list of companies making significant use of injection wells for disposal of SARA chemicals for the reporting - year TQfln beyond. The company wiR demonstrate ^
by Wrb.ifing in 1906 an 8Q percent reduction" ~
of injected SARA chemicals against the 1990 base
reporting year.
To be prepared for the possibility of mandatory ----------- :
regulations, the company intends to select by the end of
199S optimal technical strategies for total withdrawal
from deep wells. This preparation will include study-
grade estimates to achieve non-brine, treated surface
discharge. All operating units will continue where_____
possible to challenge the technical impediments to total -
withdrawal from deep wells............
-- ----
No new uses of deep wells for hazardous or toxic ' ~ materials are permitted. A "new" use of deep wells ir defined as injection of streams from new products or the addition of substances not previously injected at that ' site. New internal or external uses of deep wells for nonhazardous wastes and nontoxic chemicals will be considered by the Environmental Policy Committee (EPC) only on an exception basis and within the__ __ ~CPUSUaims of these guideline Th^-wrmnmics of anv
1.4Polychlorinated Biphenyls-`YCB-Free'*/
All company-owned sites (e.g., warehouses, plants, offices) located in the United Stales will minimize the potential for releases of polychlorinated biphenyls (PCB) by becoming "PCB-free" of Toxic Substances Control Act (TSCA)-conlaminated articles by the end of 1994.
hazardous, the company will take into account public expectations, emerging trends and worldwide company practice regarding the same or similar wastes.
Contractors hired for land disposal of wastes will be
subject to contracting and assessment requirements (see
Pledge Guideline No. 7, Outside Processors). In the
United States, the use of off-site hazardous waste
. landfills will be approved by the-EnvironmentaLRolicy^sag ^ ^
" Committee and wiRbe limited in number.
. --
Medical wastes generated at the company's locations -- will be incinerated prior to land disposal of residues.
Assurance of incineration will be obtained via manifests or equivalent documents if manifests are not available.
Each company location will maintain a record of both..........
the on-site and the commercial waste treatment, storage
and disposal sites it uses. __ ;
-----------
--------
1.6 Air Emission and Water Release Assessments
The company will conduct and maintain an ongoing assessment of potential hum^itey<qiams Cdc^L ;~. selected, routinely emitted air pollutants. It will develop appropriate control strategies to reduce identified, potentially unreasonable risk of harm to human health in surrounding communities. The list of air pollutants to be studied include: a) those listed under Section 112(b) of the U.S. Clean Air Act; b) those for which the usepa established cancer unit risk values; c) those
on-rhp-tnK-rm^wlAecncv for Researchon
TIXRQgHJup 1 and 2A lictsid)-other The-- -- spccrtic pollutants lueuuneu by the (Hint that api*au> warrant consideration (including those in significant quantities reportable via SARA Section 313). Plants outside the United States will use the above-given pollutant list plus any additional air pollutants on any local regulatory list that the plant manager deems important.
1.5 Land Disposal
Landfill of "acutely hazardous" wastes1 and "incinerables"1 will not be practiced. For hazardous wastes and wastes managed as hazardous, fixation of particularly mobile, persistent or bioaccumulative wastes will be accomplished whenever warranted and feasible. In making the decision to manage wastes as
Each plant will maintain a list of all such air pollutants, ranked by established and approved protocols. Depending upon the pollutant's relative ranking and if required by the protocols, the plant will use appropriate dispersion modeling techniques to determine potential maximum downwind concentrations for each such pollutant at specified receptors representative of the exposed population utilizing appropriate dispersion
1 As listed is 40 CJ-K 261.33(e), plus say mixtures costxioia( greeter thee S percent. 1 Hazardous wastes, or wastes managed as hazardous, with a beat of eombustioe greater thas 6000 BTU/lb.
MPG 1. Pape 2 of 3 Company Confidential
DSH 107937
WATER_PCB-SD0000021482
modeling techniques. Appropriate assessments of potential human health impacts at the community receptor points will then be analyzed according to protocols established by the company's Environmental, Safety and Health staff1. Any potentially unreasonable risk to human health that is identified will be expeditiously reduced to acceptable levels through appropriate actions.
"The ,, . determine the measurable impacts, if any, of its effluents on receptor water quality. The assessments should include both direct and indirect discharges (if applicable) with the mitigating impacts of the publicly owned treatment works (POTW) taken into account for the indirect discharge assessments. Any potentially unacceptable impacts to the aquatic environment identified will be mitigated in a timely manner. A reconfirming assessment will be conducted to verify that the impacts have been reduced to acceptable levels.
All initial air emission and surface water release ___ . assessments required should be conducted for each of the company's worldwide manufacturing sites within two years of the EPC's approval of this guideline. . Operating units will review the status of the assessments annually, and if any significant changes have occurred at a plant site, determine whether the assessment should be repeated. Any such reassessments will be completed within 12 months.
hazardous waste streams and toxic SARA
Section 313 chemicals.
1.7.5 Air Emissions and Water Release Assessments
The company's air and water steering committees will be responsible for tracking the air emission and water release environmental _randucted at each site and - mainimnfl an oogoinglist otthe _ . . " .. assessments' current status. In addition, each plant's environmental compliance audit will check the current status of these assessments and report on progress as part of the audit's findings.
1^ Coordinators ........
....... .........
Where clarification is required, the following
coordinators should be contacted:
....
WASTE MANAGEMENT
D. B. Redington, ESH, Corporate, A3NA
.. - (314)694-6503.
_.
ASSESSMENT C. D. Malloch, ESH, Corporate. A3NA (314) 694-8889.
(Revised and approved by the Environmental Policy
The following indicators win be used id HVStSUTB progress against this guideline:' .. ~ -
1.7.1 Annual progress toward achievement of 90 percent SARA Section 313 air emissions reduction goal.
1.7.2 Annual progress toward achievement of 70 percent worldwide SARA Section 313 chemical releases and off-site transfer reduction goal. -
1.7J Achievement of contingency planning for reduction of use of deep-well injection.
1.7.4 Annual progress toward goals involving discontinued deep-well injection of RCRA
OSH 107938
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WATER PCB-SD0000021483
WATER PCB-SD0000021484
MONSANTO PLEDGE GUIDELINE
#2
EMPLOYEE AND COMMUNITY SAFETY AND HEALTH
The company will provide a healthful and safe environment for its employees, site visitors, contractors and neighbors. It will evaluate employee health status, determine and monitor workplace factors affecting employee safety and health, and comply with both the company's workplace exposure guidelines and governmental safety andhealth regulations. It will review major capital projects to protect the health ofits people at work and that ofpeople in the community.
KEY RESULTS
Approach zero adverse health effects for the company's
employees, sitevisitonand site contractors, including
zero occupational injury and illness.
''
Certify into the United States Occupational Safety and Health Administrative's (OSHA) Voluntary Protection Program (VPP) or equivalent at all facilities where appropriate by the end of 1997.
Reduce by 50 percent the company's 1991 level of...... ~ accidental reteaserof hazardous materials from.
br^ugtiim?peraQaas bythecnd'of-H*^--:::^:^^^
PROGRAM
2.1 Health Surveillance and Assessment . . . . .
The company will monitor and evaluate the effect of work exposures on employee health by providing occupational health surveillance in all locations. The goal is to offer periodic assessments for all employees. Health surveillance and periodic health assessments will be conducted by the company or by contract health professionals in accordance with the Occupational Medicine Program as defined in the company's Occupational Medicine Program ManuaL
23. Workplace Surveillance
The company will conduct workplace surveillance to identify potential health risks, evaluate hazards based on current toxicological and epidemiological information and initiate appropriate safeguards to protect employee health.
2A Audits and Reviews
~ ........
The company will perform periodic on-site audits and reviews of worldwide operations to evaluate status of ' Safety, occupational health and industriaihygiene pro grams. It will utilize observations and recommendations to achieve and maintain regulatory and code compliance, attain appropriate technological sophistication, reduce the probability of illnesses and injuries, and support employee safety and health education.
2.4 Regulations and Guidelines ---------- --- --.....
compliance. ____
~~wflh"ltf guidelines autrguiuiuurntiir riigulatiwtf for
,
facility design, sate work and operation*! practices,
injury and illness recordkeeping, workplace exposures,
health surveillance, and community safety and health. If
regulatory guidelines are unavailable or inadequate to
protect worker health, the company will establish
guidelines where appropriate.
2.5 Data Management
The company will collect and enter workplace materials, worker exposure, work history and employee health assessment data into the Monsanto Environmental Health Information Analysis & Reporting System (MARS) data base, which will be used to perform epidemiological and other appropriate studies to evaluate worker health and enhance worker protection.
MONSANTO COMPANY
OSH 1-07933
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WATER_PCB-SD0000021485
The company will establish guidelines for classifying
and recording injuries and illnesses and monitor
company-wide performance and adherence to federal
and local regulations on recordkeeping. It will issue
monthly summaries of appropriate statistics and will
produce other publications designed to improve
awareness and to communicate relevant technologies to
the workplace. The company will develop ways to
-understand the causation of injuries and exposures as__
well as techniques for prevention.^
7: ^:
t
2.6 Loss Prevention Reviews
The company will conduct safety and industrial hygiene reviews on design, start-up and operational issues for" major new installations and expansions......................
2.7 Professional Activities
The company will advance occupational health and
safety consciousness through employee participation in
trade and professional associations and other coopera-
live endeavors.
r-'
2.8 Employee Education"------ "T :-------------- -------
2.10 Security
The company will establish security procedures and ____systems to control entry and exit of personnel and_____
materials at its sites.
2.11 Measurement
The following indicators will be used to measure
progress against this guideline: '
........
v-v- * Annual progress,toward operatingjmit's goalsjor ; 7 - the Total Recordable Rate (TRR).
Annual progress toward entry of 100 percent
. United States manufacturing and service locations
'' into VPP by end of 1997.
-
Releases as reported per the company's worldwide ------------ system.----------- -------- -- -----------------------
Systematic review of employee health and.........
____ industrial hygiene data.
___............
.....
--
2.12 Coordinators
Where clarification is required, the following
,
---coordinatorsshould be contacted: -- - -
^ JT_ ,,,, . . .
The company will provide employee training, orientation and education in safety and health.
V. E. Boyen, Director, Safety & Personal Protection, A2NG, (314) 694-6007
2.9 Contract Employees
The company will provide contract employees with any
required occupational health surveillance, safety and ~
--
hyjiw inHnrtriiwIinn In armrHanr^
iJtfcrr
--
htn A, rn^n^r/rta^PtrriTnitmsiUnf --- - -
Health and Jq/fri)!. Silas located in the United S>ttcs==
will meet the requirements of the contractor environmental, health and safety guideline.
P. A. Easterday, Director, Industrial Hygiene. A3NL, (314) 694-8836 J. H. Baker, Director, Occupational Medicine. --A3NB. (314) 694 8806----------------------------
(Revised end approved by the Environmental Policy Committee, October 22,1992.)
M PG 2. Page 2 of 2 Company Confidential
OSW 107940 WATER PCB-SD0000021486
MONSANTO PLEDGE GUIDELINE
#3
PROCESS SAFETY AND EMERGENCY RESPONSE
The company will research, deoelop, design and operate processes in a manner that protects the health and safety ofemployees, site visitors, contractors and neighbors. Beyond compliance with appropriate governmental regulations, the company will apply such standards andprograms as necessary to manage operationalrisks at a level that ensures its continuing right to operate. All company sites will complement this effort with strategies to mitigate risk in the event ofan incident, including site emergency response andsupport ofcomparable efforts within the community.
......... KEY RESULTS
Sustain oo major losses from catastrophic incidents.
Retain the company's inferred risk status mth insurers.
Reduce by SO percent the company's 1991 level of accidental releases of hazardous materials from production operations by the end of 1996.
Incur no major injuries to employees or neighbors from
" a plant process incident.-
-------------- --
designs. Designs should incorporate relevant consensus standards as appropriate. Additionally, the Safety and : Property Protection (S&PP) staff shall provide -'" supplemental guidance through Design Guides, Tecfacts and related documents (e.g,, Guidance Notes as published by S&PP, Europe/Africa).
3J Project Reviews
All projects (new processes, products or facilities) will undergo safety reviews to ensure adherence to applicable ------ internal and external standards as well astaexaminethe
3.1 Process Development and Design
Every new process will be characterized in a document (e.g.. Tentative Process. Red Book. Processfor Engineering Design) that describes all materials, equipment and processing conditions, including known safe limits. Design and engineering will be based on such documentation for a new process and on existing operations if there is already an established process. The basis for design of all major operating components and critical safety systems will be recorded in a design manual. Any new or expanded facility will be reviewed for its safety impact on the community.
3.2 Technical and Engineering Standards
The engineering organizations will maintain such standards as necessary to allow safe and effective
processes will undergo a research stage review. Appropriateparticipation from the Environmental. Health and Safety (ESH) staffis required for projects managed by an operating unit's engineering organization. All major projects should also have a pre-startup review to confirm that all recommendations from prior reviews and hazard analyses (if performed) have been addressed.
3.4 High Hazardous Materials (HHM) Program
High Hazardous Materials (HHM) are those materials, that if accidentally released would pose the greatest threat to neighbors and employees. A higher level of controls and operating standards are applied to these materials. The major elements of the HHM program include the use of Hazard and Operational Study (HAZOPs). the preparation of a guideline document for each HHM, and audits once every two years.
MONSANTO COMPANY
DSW 107941
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WATER_PCB-SD0000021487
3.5 Operational Safety Management
Safe process operations on a continuing basis are main tained by each site by the company's commitment to a series of fundamental practices. Included are the following:
3.5.1 Operating Procedures Written procedures are kept current for all processes. They cover necessary operating instructions, safe handling of materials, safe operating limits, and responses to deviations, including emergency steps.
3.5.2 Operator Training All production and maintenance operators must undergo training to acquire the necessary skills and knowledge for safe execution of their responsibilities. Operators most adequately demonstrate their competence before they assume their positions; training must be periodically reinforced.
3.5-3 Contractor Safety .. ___The company will provide contract employees
with any required occupational health survefllance, and safety and industrial hygiene indoc trination in accordance with Other Guideline No. 6, Contractor/Guest Environmental. Health and Safety Guideline. Sites will meet the requirements of the contractor environmental, health and safety guideline.
--3,5.4 MaNAGEMENTOF Change "
Any rhino# in
pmrrrre
"~ 1
recognized as the safe operating regime shall be governed by a "management-of-change" protocol to ensure proper safety review, authorization, training and implementation. This protocol also will apply to capital projects on all changes made subsequent to the previous safety review. A separate protocol will apply to changes in the tine organization.
3-5-5 Critical System Inspections A program involving inspection, replacement and/or testing of critical equipment or safety systems must be maintained in order to ensure reliable operations and system integrity.
3.5.6 In-Depth Process audits At intervals not to exceed three years, all operations shall undergo intensive audits to examine areas of change, non-routine occurrences, new information and other
MPG 3. Pape 2 of 3 Company Confidential
unusual factors to ensure that no new hazards have been introduced and that appropriate' safety margins have been maintained.
3.5.7 Incident Investigations
All significant incidents that threatened or
could have threatened process integrity or the
well-being of involved personnel will be
investigated by a specially appointed team
who wiliestablish causes and make
recommendations to prevent recurrence.
~
3.6 Emergency Response
Effective emergency response includes not only those actions to mitigate and control the incident within the fenceline but also includes actions that address the potential impact on the community. Consequently, a site emergency response program should include the following elements; ......
3.6.1 Emergency Procedures Written emergency procedures will be
- available and kept current for each process, as - - well as for the total site. They will cover
actions at each stage of the emergency including shutdown and evacuation. All employees must be trained in these procedures.
Emergency Drills: - Site managers will test and audit their ----------- ------ emergency plan annually and revise it as
r ~11 --necessary. At intervala detenniDcd by the, sild, me emergency drilHwBTnghidMhe --.
' active mvoivetueut uf mmummlj fflsourmti - associated with emergency management
3.6.2 Community Preparedness The site managers will review with appropriate community officials the nature and extern of potential incidents from the site and provide the community with assistance in emergency planning if requested.
3.7 Measurements
The following indicators will be used to measure progress against this guideline:
Annual progress reports on S&PP Compliance Audits, the HHM Report of the Monsanto Manu facturing Council (MMC) once every two years and site ln-Depth Process Safety Audit Reports.
osw lO79**2
WATER_PCB-SD0000021488
Annual cost of property and business interruption insurance.
Monthly reports on SARA Title III. Section 304. reportable releases against goals.
. S&PP quarterly property-loss reports.
3 8 Cwirdlnatoc-~
--
Where clarification is required, the following coordinator should be contacted:
~
V. E. Boyen. Director. Safety & Personal Protection. A2NG, (314) 694-6007
3.9 Definitions ESH: Environment. Safety and Health. HAZOP-. Hazard and Operability Study, a hazard identification technique. HHM: Highly hazardous material (a Monsanto designation for substances posing an acute risk). MMC: Manufacturing Management Council. 5X/M; Superfund Amendments and keauiborizaiioit Act.
(Revisedand approved by the Environmental Policy Committee. October 22,1992.)
OSu lO?9*3 MPG 3. Pace 3 of 3 Company Confidential
WATER PCB-SD0000021489
.
____
_____ _________ ______
MONSANTO PLEDGE GUIDELINE
.......................................................................
.
#4
PRODUCT STEWARDSHIP
The company will research, develop, design, assess, manufacture, market and dispose ofits products so that they meet societal needs and do not pose undue risk to human health or to the environment during all stages oftheir life cycles. The company will work with product stake holders (suppliers, employees, distributors, customers, consumers and disposers) to understand and reduce risks associated with the life cycle ofthe company's products.
KEY RESULTS
--------- Practice the principles and key elements of Product
- Stewardslnp, as specified mjinpipp*i?te
around the world, at all the companyVgldbal
-
operations.
'
Provide appropriate safety and handling information,
including Material Safety Data Sheets (MSDSs), to
potentially exposed employees, including contract
employees and product receivers.
----- Work toward-the goal ofno-undue risk through.________
RAD and prior to off-site shipment. A product-risk characterization (including an EC-202 or equivalent, a final MSDS and a - ...... shinning classification) will be completed before new product commercializaaon.
4.1.2 The company's process for generating and mainlining an MSDS is comprehensive and. when coupled with human experience and professional judgment, will fulfill the requirement for a product-risk
characterization. Whenever significant new
Gain a competitive advantage by applying product stewardship principles that add value to the company's product offerings.
PROGRAM
4.1 Environmental, Safety and Health Information and Risk Characterization
4.1.1 New chemical products, new isolated process intermediates, and significant new uses for existing chemical products will be accompanied by adequate environmental, safety and health exposure information to support a preliminary product-risk characterization (ER-200 or EC-201, and an RAD MSDS) at the earliest practical stage of
satisiy regulatorj UK1 product ink characterization requirements. An MSDS review/product-risk characterization will be periodically performed commensurate with product risk, with revisions performed at a minimum, every five years.
4.1.3 Product files or information systems will be maintained for all products or product families. The product files or information systems will contain the data necessary to fulfill regulatory requirements and perform product-risk characterizations and assessments as appropriate, including:
Material Safety Data Sheets:
References to relevant literature or internal reports dealing with health and
1Material Safety Data Sheets (MSDSs) and Safety Data Sheets (SDSs) are interchangeable terms, and refer to the similar requirements in different countries.
MONSANTO COMPANY
-
DS M 10 79.4 4
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WATER PCB-SD0000021490
safety (toxicology, epidemiology, indus trial hygiene, flammability, reactivity, etc.), relevant information on composition, physical properties, raw materials, manufacturing processes, principal by products. protective measures, exposure information, energy requirements, wastes and disposal practices; .
432 Pollution prevention principles (Pledge Guideline No. 1, Pollution Prevention) will be included as review criteria in technology-risk reviews for new and existing chemicals, and will be incorporated into the EC-201/202 (or equivalent) assessments.
4.4 Employee Education and Product Use Feedback
... --......* Information on use, including handling. 1 . _______4.4.1 Employee education in the safe handling and
transport, packaging and storage, which will
use of chemicals is addressed in Pledge
either be estimated (typically for new
~ Guideline No. 2, Employee And Community
products), or obtained by visits or reviews
Safety And Health.. Employees with
of customer, distributor and consumer
significant customer interaction will be
practices;
trained to recognize and feed back
A critical review of health aqd environmental effects and exposure
------- ___
information about product use and misuse to the company's environmental network.
information, such as EC-201, EC-202,
4.4.2 Feedback systems to listen to stake holders,
Monsanto Work-Place Permissible ........
including commercial and technical service
Exposure Guideline (MWPEG) Reviews,
.......
liaisons with customers, product hotlines.
Health Effect Reviews and Toxicology
poison control center relationships, etc., will
Reviews;
be nurtured and expanded as appropriate.
Technology Risk Reviews;
Health concerns of customers, employees or the public.
4.5 Contract Manufacturers
......... -.........
See Pledge Guideline No. 7. Outside Processors.
4.2 Risk Management System
In addition, the company will provide guidance and information to contractor personnel on the safe handling
4.2.1 A systematic approach to risk management
and transportation of company products.
will be implemented and maintained for new
~ ~ productsv~xistingpcoducts will be managed------- 4.6 Suppliers___ ___
___ ____ __
oa i casc-by^cascbasts.
--..* '*' Bl|,|f mni'njPMiin
whe needed. --
will be an integral part of the follow-up to
n 4.6.1 Up-ftPttaigand high-qualityproduct--^------
=-
-tnfarmatkMMnduding, as approjfffifilZZZZ
. composition data and MSDSs, will be
each phase of a product-risk characterization
obtained from suppliers for all raw materials.
(as detailed in Section 4.1).
4.2.3 All products will be appropriately labeled for hazard or risk, and will conform at a
4.6.2 Suppliers will be actively engaged as appro priate, commensurate with raw-material risks.
minimum to governmental requirements and
appropriate consensus standards (e.g., ANSI.
ISO, etc.).
_
4.2.4 Document risk-management actions will be recorded in product files (examples of specific risk-management actions are detailed in Sections 4.3 through 4.7).
4.7 Distributors, Customers and Other Direct Product Receivers
4.7.1 The company will ensure that MSDSs and other appropriate safety documents are provided to all direct product receivers.
4.7.2 As appropriate, the company will actively involve product receivers in dialogue and
43 Product and Process Design and Improvement
4_3.1 R&D materials used in the laboratory will be handled under Prudent Laboratory Practices or equivalent guidelines.
outreach regarding appropriate risk characterization, risk management and risk reduction. Where applicable, the company will assist in conducting audits. If improper
'nvolving company products are
MPG 4. Pace 2 of 3 Company Confidential
OSM
WATER_PCB-SD0000021491
identified, (he company will work with the ' product receiver to improve the practices. If
adequate improvement is not evident, the company will take appropriate action, including termination of sale if necessary.
4.7 j The company will actively seek productreceiver involvement in the continuous improvement of company products and as a means of differentiating those products in the marketplace on the basis of environmental, safety and health stewardship.
4.8 Responsibilities
4.8.1 Product stewardship is the responsibility of the business units. Each operating company, free standing division or world area will assign certain employees the responsibility for ensuring that this program guideline is met. i.
4.8.2 Guideline overnight is the responsibility of the
corporate Environmental. Safety and Health
staff.
..........
4.8.3 The corporate staff and business units are jointly responsible for developing information needed for product evaluations. This includes periodic re-evaluation of new information relevant to the product on a regular basis.
4.9 Measurement fh*~fnnmng m/tit-ators will he used to measure progress agatmrthh gtridetinet
4.9.1 Progress in meeting internal and external requirements for all new product introductions (i.e., EC 201/202 approvals and governmental approvals).
4.9.2 Progress in determining product hazards.
4.93 The growth of knowledge about bow company products are used and the resultant exposures to people and the environment
4.9.4 The availability of
environmental,
safety and health data to the ultimate product
receiver.
4.9.5 Increased understanding and diminution of the risks and environmental impacts associated with a product throughout its life cycle.
4.9.6 Differentiation of company products in the - -- -
4.10 Definitions
Product Receiver: An entity (not an individual) to whom the company transfers product. This definition includes product receivers such as brokers or transporters who may not fall into the traditional customer category.
. Product: Chemical substances mod mixtures,
materials and equipment, articles, licensed
technology and services related to product use that
are sold, distributed in commerce, or otherwise
: . provided.
.
.......... - ; r
4.11 Coordinator
Where clarification is required, the following coordinator should be contacted: .
J. R. Condray. ESH. Corporate. A3NA
(314)694-8883. ------
---------------
OSW 107946
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WATER PCB-SD0000021492
. __ ___
MONSANTO PLEDGE GUIDELINE
#5. .
CHEMICAL DISTRIBUTION
The company will reduce potential risk to its employees, the public, carriers, distributors, contractors, customers'employees, and the environment in the distribution ofchemicals.
KEY RESULTS
Work toward incident-free performance in the distribution of chemicals, including raw materials, intermediates, finished products, byproducts and wastes.
.....
PROGRAM
...
5.1 Chemical Distribution Incident Reduction .
5.1.1 The company will continue to improve chemical distribution in order to effect incident-free performance. An "incident" is defined as any undesirable event occurring during a chemical
7~ distribution process over which the company has dtrecregtfttoi or tnnuencraimesuhsin an tnjury.a^runn nf a chemical, anrtfnr damage ISLggBgffjg------the environment
5.1.1.1 The company will improve the carrier selection process so as to identify and contract transportation services with those carriers who consistently demonstrate safe performance in the movement of the company's chemical products.
5.1.1.2 The safety of chemical transportation practices wifi be continually improved through application of Total Quality/Total Partnership concepts and tools to achieve the company's goal of incident-free performance.
5.1.1 J The company will continue to support The Agricultural Group's Bulk No-Spill Delivery Program.
5.1.1.4 The company will develop and apply technological advancements to improve
. . etwmifai distribution safety and will share these with the industry as appropriate.
5.1.1.5 Through its emergency response system, the company will provide technical advice and
~ assistance in a responsible and timely manner for "outside plant gate" incidents involving its chemical products. The company will measure and continuously improve its response capabilities. Trained personnel will be physically present, in an expeditious manner, at the emergency site upon request
: of the local emergency responder or public .^ ^ _jifl5ciaL orwhen t^ company feels a . . ---------qualifiedemergency team can, lessen die.
seventy of iii mudeut ui alii u nity's concerns about the company's products.
5.1.2 Procram Emthasis Areas
5.1.2.1 Each shipping location will have a current plan for responding to chemical transportation emergencies involving products/materials within its scope. The plants* emergency responders will receive regular training that meets or exceeds regulatory or industry standards.
5.122 Training history for all emergency response personnel will be documented.
MONSANTO COMPANY
OSW 10794.7
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WATER_PCB-SD0000021493
5.1.2-3 The company will discuss with emergency responders and the public their concerns about chemical distribution. The company will encourage partnerships with local communities and local emergency responders along chemical transportation routes, as well as in those communities where its chemical plants are located.
5.1X4 The total emergency response plan will be continuously monitored and improved. Detailed post-incident reports and preventive action plans will be provided as training aids to all emergency responders. -
-
5.1.2.5 Distribution accidents/incidents and any resulting loss of containment will be reduced according to a documented distribution riskmanagement methodology. An initial
.................. qualitative risk-assessment methodology will be made available for use. Quantitative risk assessment models will be evaluated for especially sensitive materials.
_ 5.1X6 Regulatory changes (hat affect the
___
distribution of the company's products will
be monitored and changes will be
.
communicated to shipping locations.
Compliance audits and training will be
conducted at all company shipping locations
as appropriate and reported on annually.
5.1X7 The company will support community ------nmmarii programs hy nqfojng plant
--facilities and mutual training to those------- emerBencyiespuutleis'uicuuuuunities neighboring the company's distribution network.
5.1.2.8 The company will, as appropriate, through routine communications with the public, emphasize continuous improvement in safe chemical distribution and will be responsive to public concerns.
5.1X9 As appropriate, trained plant employees will be the company's "ambassadors** to the community to convey the company's progress and its commitment to improving the safety of chemical distribution and effectiveness of its emergency preparedness and response.
5.1X10 The company will recognize, as appropriate, the potential for adding value to its products.
52 Chemical Distribution Safety for Warehouses and Terminals
5X1 A seamless policy of operating safety results will be extended to warehouses and terminals that receive the company's products. This policy will incorporate standards comparable to the company's.
5X1.1 The company will use precontracting guidelines in the selection process to assess firms that can handle company products in a manner that is safe for its employees, the public and the environment
5X12 The company will provide information on its policies, procedures and requirements on the safe handling and transportation of chemicals to warehouse and terminal personnel.
5X1J The company will apply Total Quality
............
Management concepts and tools to all
aspects of contract management for
continuous improvement in safety and
reliability of provided services.
5X1.4 The company will use agreed-upon performance measurements and periodic reviews as indicators of progress toward zero-incident status.
5X1.5 The company will extend its recognition of public concerns about emergency preparedness and safe distribution practices to all its distribution locations.
-SXI Prockam Emwu.sk
~
"
5X2.1 Documented selection criteria that include appropriate safety measures for each product will be maintained.
5X2.2 The company will maintain defined flows of information concerning its policies, guidelines and requirements on the safe handling of its products.
5X2.3 The company will conduct reviews of performance against its requirements on a specified review cycle.
5X2.4 The company will support risk management activities and emergency preparedness at all of its distribution locations.
MPG5. Pape: of 3 Company Confidential
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WATER PCB-SD0000021494
5-3 Measurement
Appropriate measurement systems will ensure continuous improvement toward stated goals and objectives.
5.4 Coordinator
Where clarification is required, the following coordinator
should be contacted:
D. E. Williams, Chemical, Purchasing/Distribution,-------------- --- ------------------- --------------------- -- ----BRSS.F2EA, (314) 694-8644.
(Revised and approved by the Environmental Policy
Committee, October 22.1992.)
.
OSM 107949
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WATER PCB-SD0000021495
J8j& MONSANTO PLEDGE GUIDELINE
.
#6
GROUNDWATER AND SOIL QUALITY
The company will design and operate facilities to protect groundwater and soil quality. The company will assess groundwater and soil quality at its facilities and pursue remedies for releases that threaten health or the environment. The company will address on-site and off-site contamination ofground water and soil attributable to its `operating and waste practices to ensure protection ofhealth and the environment.
KEY RESULTS
Establish an active groundwater assessment program
at the company's facilities.
................... _
Ensure that there are no adverse public health impacts attributable to the company's wastes.
Minimize the financial impact of remedial action and third-party liability attendant to waste sites.
PROGRAM
------------ --- could contaminate groundwater (e.g.. sewers, process lines, sumps, tanks, loading/unload
ing areas). The groundwater protection plans
and designs will be commensurable with the
------ risk posed by the specific situations.
_
6.2.2 Facility Design
New, replacement or expansion facility designs (including sewers and lines) will consider such options as aboveground and/or double containment, improved materials of construction, and/or cathodic protection to provide improved assurance against
quality will be organized at all major locatians.and it lesser sites that have known groundwater issues. Follow-up plans will address priority concerns. The assessment status and plans will be updated in a summary report during the second quarter of each year.
Any newly purchased, existing operation will be subjected to the seven-point protocol for assessment of possible groundwater contamination. The coordinator of this guideline (see 6.6 herein) will supply a copy of the assessment protocol upon request
6.2 Protection
6.2.1 Groundwater Protection Plans
Each location will maintain a groundwater protection plan that includes inspection, testing and maintenance of facilities that
New, replacementdr expanded surface impoundments for wastewater treatment or storage must be approved by the Environmental Policy Committee on an exception basis.
New storage tanks for materials that could cause contamination will be provided with impervious secondary containment (e.g., dikes, liners, vaults, double wall) unless a clear showing is made on a tank-by-tank basis during project reviews that vessel contents (e.g., dilute wastewaters) or setting (e.g.. in battery containment, other adequate containment systems) do not wanant such containment. Existing storage tanks will be reviewed in normal environmental audits.
MONSANTO COMPANY
OSH 107950
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WATER_PCB-SD0000021496
6.3 Abandoned Waste or Groundwater Contamination
When on-site abandoned waste or groundwater contamination is discovered, appropriate assessment of impacts on human health and the environment will be earned out. Corrective action will be taken, as necessary, in a planned, orderly process to remediate soil and groundwater impacts that threaten, human health and the environment.
6.4 Superfund
1
~
The company will act to ensure that there are no public health impart^ attributable to its wastes at "Superfund" sites.
6.5 Measurement The following indicators will be used to measure progress against this guideline:
6.5.1 Submission of annual groundwater assessment summary reports by each plant subject to reporting.
6.6 Coordinator Where clarification is required, the following coordinator should be contacted:
D. B. Redington, ESH. Corporate. A3NA. (314)694-6503.
When the company becomes aware of involvement in
"Superfund" sites, it will actively participate in potentially responsible parties' efforts to achieve......... settlement. The company will seek a leadership role,-----when appropriate, to facilitate resolution. The operating units will cooperate to establish responsibility for sites where several units contributed wastes, and will undertake an oversight role for sites funded at the corporate level when no current operating unit has responsibility. A goal of the company is to resolve as ' soon as reasonably possible its share of liability and remedial plans for sites where it has a responsibility, while securing timely and cost-effective resolution.
(Revised and approved by the Environmental Policy
Committee. October 22,1992.)
...........
The company intends a lessened legalistic approach to
site cleanup negotiations. Where company
.. ' ` ; .. .
responsibility isfairlv estaMishriOhecSmihv^flfnSr'.........
delay ctearopunnecessarityby lcgal.yet negatively ~____ -
perceived litigious steps. The company will pursue fair
legislation and regulations on the general issues in the
public arena, but minimizing legal risk will not be the
determining factor in (be site-spedfic decisions.
MPG 6. Pape 2 of 2 Company Confidential
OSW 107951
WATER PCB-SD0000021497
# _____________ ___
___
MONSANTO PLEDGE GUIDELINE
#7
OUTSIDE PROCESSORS
To support its operations, the company willselect outside processors that will operate with concern for worker safety, regulatory compliance, community protection and protection of the environment.
KEY RESULTS
Manage the company's exposure to present and future liabilities associated with the use of outside processors by maintaining current assessments and written contracts for each outside processor used.
PROGRAM
7.1 Outside Processor Selection The company will use only outside processors that have been selected and periodically assessed to ensure the following:
a. their ability to protect the public, employees and the .. . ^ environment adequately from any adverse effect of "-- the company's chemicals, products or wastes: " '" ~ ^
b. their compliance with all applicable Iawsan<F^~~~ regulations:
c. their knowledge of potential hazards and any applicable manufacturing requirements associated with the handling of company materials; and
d. their use of waste disposal methods and locations as specified in contracts, with recordkeeping of all material use and waste disposal.
Before they are used by the company, outside processors will be subject to contracts and on-site assessments and approval by the appropriate operating unit or subsidiary director of environmental operations and its manufacturing director or world area designee. Periodic reassessments will be conducted for continuing use.
Procedures will be maintained to define the types of outside processors subject to this program, the assessment protocols and frequency, the conditions for waiver of one or more of the above requirements, and other standards.
For toll manufacturing, bulk terminals and transloading, the outside processors will take title to, adopt and own the wastes and manage them as their own under manifests and contracts. For other outside processor categories (waste management, cleaning services, etc.), a processor's waste management practices will be reviewed as part of the on-site assessments.
Outside processors used by all operating units, ^--subsidiaries anttworldareas, will.bcjecorded in one or
more databaseslqivokfredundant assessments and - contracts and to fatiKtateuse~bf approved processors~ ~~
The above elements will be implemented worldwide, but with modifications to reflect local limitations, restraints to compliance with this program, and the extent of the company's operating control. Status and direction of the local program will be reviewed in planned environmental audits of the company's facilities outside the United Slates.
7.2 Measurement
'
Each operating unit, subsidiary and world area will maintain records that document the number of outside processors used, the number of outside processors for which assessments are current, and the number of outside processors with contracts in place.
MONSANTO COMPANY
OSW 107952
MPG 7. Page 1 of 2 Company Confidential
WATER_PCB-SD0000021498
7J Coordinator Where dariflcation is required, the following coordinator should be contacted:
D. B. Redington, ESH, Corporate, A3NA, (314) 694-6503.
(Revised and approved by the Environmental Policy Committee. October 22.1992.) '
MPG 7. Pap. of 2 Company Confidential
>SW 10 7953
WATER PCB-SD0000021499
i&fy. MONSANTO PLEDGE GUIDELINE
#8
COMMUNITY AWARENESS AT MANUFACTURING SITES
The company will foster its employees'and the public's right-to-know through a commitment to openness, involvement and community dialogue. The company will be responsive to questions and concerns about human safety, health and the environment at its manufacturing sites.
KEY RESULTS
Establish active community advisory panels, as appropriate, at manufacturing sites.
PROGRAM
8.1 Community Involvement and Dialogue Each manufacturing site will implement a policy of openness that provides convenient ways for interested individuals to become familiar with the facility, its operations, its products and its efforts to protect human safety, health and the environment Community advisory panels, open bouses, plant tours, environmental
- community in plant operations may bemused. " _____~
Community outreach programs will be implemented at each manufacturing plant to informkey audiences (emergency responders, government officials, the media, employees, other businesses and the community) about the facility's emergency response program, chemical inventory, impact evaluation, and potential risks to the community associated with the facility. The information provided will include details on such topics as waste minimization, emissions reduction, health effects of chemicals, and efforts to ensure safe transport of chemicals.
Further, all information will include planned improvements in each of these critical areas as well as expansion activity and other projects of general interest to the community.
An ongoing dialogue with employees and members of the community will be used to assess and respond to their questions and concerns about environmental, safety and health issues, and to involve them in the community outreach effort Each manufacturing site will conduct an ongoing assessment of employee and community questions and concerns about the site. The effectiveness of the ongoing community communications effort will be evaluated regularly by the site.
Communications training will be provided for key site and company personnel who communicate with employees and the public concerning human safety, health and the environment
8.2 Information on Chemical Releases/Incidents .
Each operating location will make available timely ~ ~ information about routine or accidental releases of toxic chemicals and other chemicals of local concern. Appropriate audiences may include neighbors in the community, employees and the news media. Informa tion will also include progress in achieving the company's stated emissions reduction and pollution prevention goals and future plans. When possible, the information on chemical releases should be at a personal, face-to-face level, and should emphasize listening to others and discussing their concerns and ideas.
The company will publish and distribute annually an Environmental Annual Review that articulates the company's environmental, safety and health policies and its progress toward achieving stated environmental, safety and health goals.
MONSANTO COMPANY
DSW 10 7954
MPG8. Pace 1 of2 Company Confidential
WATER_PCB-SD0000021500
8J Measurement
The following indicators will be used to measure progress against this guideline:
Annual progress toward establishing community advisory panels, as appropriate, at each manufacturing site.
Annual dissemination of data on toxic chemicals and other chemicals of local concern at each manufacturing site, as appropriate.
Annual report of the company's status against stated environmental, safety and health goals through wide distribution of the Environmental Annual Review.
Progress, as appropriate, toward developing routine and convenient ways for interested parties
____ tobecome familiar with the company's manufacturingsites, its operations, its products, and its efforts to protea human safety and health and the environment.
8.4 Coordinator Where clarification is required, the following coordinator should be contacted:
G. F. Barton. Corporate Communications. A2SP (314) 694-7233.
(Revised and approved by the Environmental Policy Committee. October 22.1992.}
Ml'G f>. Pace: of: Company Confidential
sw 107955
WATER_PCB-SD0000021501
OTHER GUIDELINE
#1
ENVIRONMENTAL, SAFETY AND HEALTH REVIEWS
OF CAPITAL PROJECTS
The company's capital projects will meet the Monsanto Pledge Guidelines, and will be in compliance with existing and anticipated governmental regulatory requirements. The company will review at all levels capital projects for environmental, safety andhealth impact before, and as a condition of, project funding.
The vice president of Environmental, Safety and Health or his designee will review those projects requiring approval by the chief operating officer, the chief executive officer or the board of directors. A formal -----premise review will be held for such projects or other projects with major technology changes as determined by the operating unit, technology and engineering directors. A system for reviewing other projects will be administered by the directors, environmental operations, of the operating units.
Any exceptions to this guideline must be approved by the Environmental Policy Committee,
--; ... ____
_____ ___
(Revised and approved by the Environmental Policy Committee, October 22,1992.)
^feaptoyees-assigned mavalnair. a new location for _ operation wilTpfepafe an internal environmental impactassessment addressing potential environmental' "'r ~ limitations at the site as a result of the existing socioeconomic and biophysical conditions. The effects of the public climate of opinion and of existing and future governmental, environmental regulations that may apply also are to be considered.
MONSANTO COMPANY
SU 1079.56
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WATER PCB-SD0000021502
OTHER GUIDELINE
. #2
ENVIRONMENTAL, SAFETY AND HEALTH REVIEWS OF DIVESTITURES OR ACQUISITIONS OF PROPERTY AND/OR BUSINESSES
Negotiations for acquisition or divestiture of property or business units and the securing of final corporate approval are the primary responsibilities of the involved operating unit However, corporate staff review of " environmental, safety and health factors and any attendant liability issues is required during the course of such transactions. This review should be arranged through the office of the operating unit's director of environmental operations, who will, in turn, involve appropriate Environment, Safety and Health staff and Environmental Law personnel and arrange for review by the vice president of Environmental, Safety and Health, and/or the executive vice president of Environmental, Safety. Health and Manufacturing. The review should be completed prior to seeking board of directors approval.trfthea^uisiftpnhrdlvesQturer""'''"^^ " ' --
(Revised and approved by the Environmental Policy Committee, October 22,1992.)
MONSANTO COMPANY
DSW 107957
OG 2. Pape 1 of 1 Comoanu Confidential
WATER_PCB-SD0000021503
OTHER GUIDELINE
ENVIRONMENTAL, SAFETY AND HEALTH PROTECTION
FOR INVESTMENTS OVER WHICH THE COMPANY
DOES NOT HAVE OPERATING CONTROL
The Monsanto Pledge Guidelines apply at all sites worldwide where the company has operating control. For those investments over which the company does not have operating control, at a minimum, compliance with applicable local laws, regulations and practices will be required.
If such applicable rules and practices do not provide environmental, safety and health protection that would be acceptable for company-controlled sites, the company will initiate action to bring about the necessary upgrading.
#3
(Revised and approved by the Environmental PoUey -------- -- .... .
Committee, October 22,1992J
I . ' '.""'.TTIirr .7.1*'"'.""'
... `--
MONSANTO COMPANY
OSM 10 7958
OG 3. Page 1 of 1 Company Confidential
WATER PCB-SD0000021504
OTHER GUIDELINE
#4
REPRODUCTIVE HAZARDS IN THE WORKPLACE
The company will use all appropriate information to ensure avoidance ofreproductive effects in workers ofboth sexes and in offspring ofworkers.
Through the departments of Medical and Health Sciences and Safety and Environmental Health, the company will do the following:
The company will conduct appropriate toxicological tests of its raw materials, products, intermediates and byproducts.
The company will review current literature for information on the hazards of chemicals and physical agents that the company uses or produces.
The company will assess safety and health
implications and the potential reproductive
------- hazards posed by these chemicals andphysical
' agents.
.- -
The company will minimize exposure to potentially harmful materials or activities by substitution with less risky chemicals or processe when feasible, through the use of engineering, work practices, and reliable protective equipment
The company will provide the most accurate
information currently available on materials or
work practices thought to have reproductive
health effects------- ------ .... .
_.....
The company will offer counseling by qualified health professionals to employees about workplace reproductive concerns. . . .
(Revised and approved by the Environmental Policy Committee, October 22.1992.)
MONSANTO COMPANY
OSW 1X17959
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WATER PCB-SD0000021505
OTHER GUIDELINE
#5
, SAFE HANDLING OF CARCINOGENS
The company will provide safe and healthful working conditions for its employees. It will comply with all governmental regulations concerning exposure to carcinogens.
'The company will do the following laensure the safe handling of carcinogens:
If any data suggest that a chemical to which its employees are exposed is a carcinogen, and such chemical is not subject to governmental regulations, the company will evaluate those data and then take appropriate action........................
If the data establish the chemical as a human . carcinogen, the company will take appropriate action to reduce exposure to the lowest reasonable level, unless exposure is already at such a level.
If the data establish the chemical as an experimental or suspect carcinogen, the company will (individually or with others) initiate a study to confirm or disprove such designation. During each study, exposure will be reduced to and/or minimized at the lowest reasonable level.
If it is concluded that a material cannot be produced or used without jeopardizing employee health, its manufacture or use will be discontinued.
(Revised and approved by the Environmental Policy Committee, October 22,1992.)
MONSANTO COMPANY
OSW 107960
OG 5. Page 1 of 1 Company Confidential
WATER PCB-SD0000021506
OTHER GUIDELINE
#6
CONTRACTOR/GUEST ENVIRONMENTAL, SAFETY AND HEALTH
Continuous improvement in contractor/guest environmental, safety and health performance is necessary to create an injury-free and incident-free environment at altcompany sites for employees and their guests.
6.1 Scope This guideline sets forth environmental, safety and occu pational health (ESH) guidelines applicable to contractors and guests who perform services on or visit company property. All services administered by individual sites or by company engineering groops are covered. _ Deviations Grom the contractor/guest ESH process and requirements will be thoroughly documented and . approved by the location manager or as described in the ContraaorAJuest ESH Guideline Manual. No deviation from regulatory requirements will be permitted.
This guideline applies initially to all company locations in the UnitedSutes.'nie intent is to work toward . .. worldwide implementation. . .. .. .. .... .
U Definitions
Contractor. Any non-company person performing physical work at a site under a company purchase order or contract
Guest: Any person visiting, performing work or providing a service at a company-managed site, including company employees who are not permanently assigned to that location. *
Certified Monsanto Representatives'. Employees designated by the location management to administer the Contractor/Guest ESH Guideline.
Master Monsanto Representative: The location administrator/facilitator responsible for ensuring effective implementation of the Contractor/Guest ESH process at the location, including training and certifica tion for other Certified Monsanto Representatives.
Contract. The document that contains terms and
conditions of the agreement between company and the
contractor and which serves as proof of their respective
obligations. Contracts are to be signed by authorized
representatives of the contractor and company, in a
form previously approved by the Purchasing and Law
departments.
....
6.3 Objective
_
The process described in this guideline was developed to
define requirements for all company locations to ensure
continuous improvement toward incident-free and
injury-free performance for employees and all
~oootnctcs andgucsts.~~ " -
------ - -------
Through this process, it is intended that all services per formed by contractors on company sites will be covered by written contracts. Furthermore, the contractor is to be made aware of the requirements of this guideline before bidding, and the appropriate requirements are to be incorporated into the written contract
In accordance with the objective of providing for employee and guest safety in the execution of contract work, the company will utilize contractors who have demonstrated a high degree of compliance with workplace laws/standards, policies and practices; have a history of good health and safety performance; maintain adequate insurance coverage; and, if involved in safety sensitive work, have a substance-abuse treatment program reasonably equivalent to that of the company.
MONSANTO COMPANY
OSW 107961
OG6, Paeelo[4 Company Confidential
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This process is designed to help ensure that the company will go beyond current regulations, take an industry leadership position in contractor/guest safety and ensure continuous improvement toward incident-free and
injury-free performance.
6.4Responsibilities
.
The location manager is responsible for ensuring implementation of this guideline. Each site will have a _ minimum of one company master-certified representative with responsibility for administering and facilitating the Contractor/Guest ESH Guidelines.
6-5 Supporting Documentation
This guideline is supported by Contractor/Guest ESH Guideline Manual that incorporates the following requirements:
Contractor Management Systems
"'
Working in an Operating Facility
,,;
Housekeeping
Fire Protection and Prevention
Hazardous Work Permits
Occupational Health/Workplace Exposure Monitoring
Vehicle Safety Waste Management .
.. _
.
Occupational Medicine , 1
r.
Management of Change
6.6 Practices and Procedures
6.6.1 The company's contractor/guest environmental, safety and health process defines a fully integrated approach to the management of all contractors and guests within company facilities. The process is not intended to restrict management prerogatives, but rather to provide the consistency to help ensure chat the Monsanto Hedge is fulfilled and the highest organizational priority is placed on the health and safety of company employees, guests and the communities in which the company operates.
OG 6. Page 2 of 4 Company Confidential
6j62 Contractor/Guest Environmental, Health and Safety Process (see Appendix 6.1)
Contractor Representative Training and
Certification -- provides for the
identification and consistent training of all
individuals with responsibilities for
selection and management of contractors
and guests working at and visiting within
company facilities.
.
Guest and Delivery Site Visit Process provides a consistent approach to the orientation and control of all guests, visitors and delivery people who enter company facilities, even those not under contract.
Pre-Qualification Process -- provides a consistent approach to identifying and
_____ selecting contractors, vendors and service providers who practice effective safety programs with demonstrated leadership and performance in their industry.
Selection and Approval Process - provides a framework for the contracting of services, which indudes the identification of all ESH requirements based on the task and the pre identified risk. The process stresses clear communication of the company's performance expectations before the contract is finalized.
Pre-Job Activities and Compliance Review - Process - defines a systematic approach
for verifying that the contractor and all of the contractor's employees meet the contractual requirements, including orientation, training, medical testing and substance-abuse screening. Plant, operating unit and job-specific expectations
are emphasized.
Work-in-Progress Process -- provides a process for the management and audit of the contractor's activities to the ongoing compliance with the company's policies, procedures and requirements. The process focuses on the cooperation between the company's certified representative and the contractor's management to achieve success ful and injury-free completion of work.
OSVi
WATER_PCB-SD0000021508
Performance Evaluation Process ~ provides a deHned process for the evaluation of and feedback on a contractor's performance, whether the contracted work is for a defined task or ongoing services. Performance evaluations are fed into the contractor pre qualification process and after evaluation contractors either remain on the pre qualification list or are stricken from it.____
6.7.2 Visitors and all delivery personnel entering the location are to be made knowledgeable of site rules and regulations.
6.7.3 All contractors and guests must communicate in English at a level of proficiency that ensures their safety and the safety of others. Exceptions to the English communication requirement may be granted only by the location manager.-----------
6.7 Contractor/Guest Responsibilities
6.7.1 The contractor/guest is responsible for
(Revised and approved by the Environmental Policy
rnmpiianca with this guideline as
Committee, October 22,1992.)
incorporated into the contract or
otherwise communicated to the
contractor in order to ensure safe
----- operations. Contractors will have a_ _ _____ competent, well-trained supervisor in
----............
-
.... .....~...........
. - charge at the site at all times when its
.
- employees or those of its subcontractors
------- are present. The company will not
'
: undertake direct supervision of
contractor employees. However, when a .
contractor employee has no on-site
. supervision, the contractor should work
- with the company's certified
representative to provide for appropriate
" implementation of this guideline.
................
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OC'rh. PaucJi*:-!
Company Confidential
MONSANTO CONTRACTOR/GUEST PERFORMANCEEVALUATION.
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OTHER GUIDELINE
#7
USE OF ANIMALS IN RESEARCH FACILITIES
The company unit ensure that all animals used in its research programs are involved in projects of
importance to society and that the animals receive humane and professionally competent care and
treatment.
_
7.1 Preamble
The company develops pharmaceuticals, consumer _ goods, agricultural and industrial products that are used to treat diseases, to grow food, and to better the quality of human life throughout the world. The company works to ensure that these products provide valuable benefits to society and are safe to use.
In conducting research to ensure product efficacy and safety, company scientists use a variety of new technologies such as computer models, cell culture systems and other processes to identify effective products early on and to detect potential health problems or undesirable side effects. However, these systems are limited because they do not fully represent the complex processes of the human body. For that reason, product research and evaluation requires the use of laboratory animals.
All company research with animals is conducted under the review and supervision of Animal Care and Use Committees (ACUC) appointed by senior management Each ACUC consists of scientists, veterinarians, at least one non-scientist, and at least one person not affiliated with the company. The committees regularly report their findings to senior management and appropriate governmental regulatory officials.
The vast majority of animals used by company researchers are rabbits, rats and mice. Rodents account for over 90 percent of all research subjects. The remainder includes dogs, pigs, sheep, cattle, goats and occasionally monkeys. Laboratory animals are purchased from companies that raise animals specifically for research. Livestock are purchased from commercial farms. The company does not buy animals from pounds or shelters.
7.2 Animal Research
The company requires all scientists, technicians and managers associated with animal research programs to be fully cognizant and supportive of the specifics and spirit of this guideline.
The facilities and management programs established to support company animal research are directed and monitored by an attending doctor of veterinary medicine. The company's programs are fully accredited by the American Association for the Accreditation of Laboratory Animal Care (AAALAC).
13 Procedures
All company research animals are assigned to a specific protocol under the direction of a principal investigator. Before research can commence, each protocol is reviewed according to procedures prescribed by governmental regulations and adhered to by the ACUC. Each protocol is then reviewed and approved by an attending veterinarian and the ACUC. Records of research use and routine care are maintained for each animal. The company's goal is to give the highest consideration to the well-being of all animals used in research.
MONSANTO COMPANY
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7.4 Facilities
The company conducts all animal research in modem, well-maintained facilities that meet or exceed all regulatory standards. The company's animal facilities are considered to be among the best,in the industry. Housing spaces include special facilities to quarantine newly arrived animals, isolation facilities, and conventional holding rooms to care for required animals. Room temperature, humidity, ventilation, lighting and oityr environmental conditions are carefully monitored and controlled.
7.5 Regulatory Review
The company is registered with the United States
Department of Agriculture as a research facility. Under
the provisions of the Animal Welfare Act, the
company's facilities are regularly inspected, and the
company files an annual report
`
7.6 Information Requests General information on the company's policy and procedures regarding animals used in research may be requested from Monsanto Corporate Communications. 800 N. Lindbergh Blvd., St. Louis, Missouri 63167. The phone number is (314) 694-7233. In general, the company's animal research facilities are not open to the public. However, visits and tours can be arranged by contacting the above address. Because of the nature of the research work under way. the company may restrict access to certain areas to ensure the health and safety of the animals. Recordings, filming, taping, photography and related activities are prohibited except as specifically approved.
(Revised and approved by the Environmental Policy Committee, October 22,1992.)
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OTHER GUIDELINE
#8
OZONE-DEPLETING CHEMICALS (CFC'S)
The company will initiate actions at all ofits worldwide sites to minimize the uses and environmental
releases ofthe chemicals subject to this guideline. It willseek out acceptable substitute chemicals,
when possible, on or before applicable compliance dates set by the site's local country laws and
regulations.
`
8.1 Scope
The following chemicals are those listed in the Montreal Protocol and are the minimum number subject to this guideline. Each company site should add to the list any other chemicals of local country concern and treat them according to this guideline in conformance with local country laws and regulations.
CFC-ll CFC-I2 CFC-113 CFC-I14 CFC-115 Haion-1211 Halon-1301 Haion-2402 CFC-13 CFC-111
CFC-112 CFC-211 CFC-212 CFC-213 CFC-214 CFC-215 CFC-216 CFC-217 Carbon tetrachloride Methyl chloroform
Company sites subject to this guideline include plants, offices, R&D facilities, sales offices, warehouses and farms, when the company owns or operates facilities or equipment that use or contain one of the chemicals subject to the guideline. This coverage includes any subsidiary in which the company is a greater than 50 percent owner.
MONSANTO COMPANY
8.2 Program
The management of each worldwide site will do the following, where applicable:
8.2.1 Develop an inventory of uses and/or equipment containing any of the chemicals subject to this guideline.
8.2.2 Establish for compliance with this guideline a plan that contains the following minimum elements:
For refrigeration equipment, replace the . refrigerant with an acceptable substitute when the equipment needs to be replaced or the original refrigerant is no longer available.
For explosion suppression and fire extinguishing equipment, replace the suppression or extinguishing chemicals subject to this guideline with an acceptable substitute when the equipment needs to be replaced or the original such chemical is no longer available. Provisions should also exist to provide for such chemical replacement after a system discharge, where practical.
After Jam 1,1994, no new refrigeration, explosion suppression, or fire extinguishing equipment will be purchased that contains any chemical subject to this guideline, if substitute chemicals are reasonably available.
tnioAi
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For process and other uses of chemicals subject to this guideline, the company will expeditiously develop plans to cease using such chemicals by Jan. 1,1996.
in advance of any applicable laws and regulations, all sites will institute best management practices to minimize the uses
_ ____ _ and environmental releases of any chemicals subject to this guideline and seek opportunities for the use of acceptable substitute chemicals.where possible, consistent with good business practices and employee safety/health considerations.
(Revised and approved by the Environmental Policy
Committee, October 22,1992.)
--
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OTHER GUIDELINE
. #9
ENVIRONMENTAL, SAFETY AND HEALTH COMPLIANCE AUDITING
The company will conduct environmental safety and health compliance audits to confirm that site management systems are in place to ensure continuous improvement and compliance with both governmental regulations and corporate, operating unit, andsubsidiary policies and procedures.
9.1 Scope
Environmental, safety and health (ESH) compliance auditing will be conducted at all worldwide manufacturing and research sites.
9.2 Criteria
Each operating company and subsidiary will be responsible for ensuring that audits are conducted in accordance with the following criteria:
9.2.1 ESH compliance auditing programs will be
consistent with the five-step auditing approach as
outlined by the outside consulting firm of Arthur
D. Little and follow protocols approved by the
corporate ESH staff.
-..............
9.2.2 ESH compliance auditors will be appropriately trained, knowledgeable of the subject they audit, and skilled as compliance auditors.
9JUS ESH compliance auditors will be independent of the location/site they audit
9.2.4 ESH compliance audits will be performed on a three-to-five year maximum cycle. The frequency for each site will depend upon the results of the last audit the degree of risk, complexity, and compliance issues at the site. The audit frequency for each site will be reviewed by the Environmental Policy Committee.
9J2JS Reports of the actual audit findings and/or recommendations will be reviewed by appropriate legal staff and distributed, at a minimum, to site managers, directors of manufacturing (or equivalent for non manufacturing locations), legal and the corporate Quality and Compliance Assurance staff.
9.2.6 Follow-up on audit findings/recommendations will be the responsibility of each operating company and subsidiary. The corporate Quality and Compliance Assurance staff will request periodic status reports of auditing and follow-up corrective actions for communication to upper management
(Revised and approved by the Environmental Policy Committee, October 22,1992J
MONSANTO COMPANY
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PROCEDURE
#1
EMPLOYEE HEALTH AND EXPOSURE COMMUNICATIONS
It is the company's intent to identify hazards ofchemical substances andphysical agents in the workplace and to communicate such hazards to employees who may be exposed.
1.1 Responsibilities
Identification of health hazards of chemical substances,
physical agents, and biological agents in the workplace
is the joint responsibility of site management, the
directors of Environmental Operations (DEOs) and
corporate Environmental, Safety and Health (ESH). Line
management is responsible for the necessary communi
cations to and education and training of employees on
such hazards.
.
Europe/Africa Specific: The director of the Department of Medical Health and Safety (DMHS) Europe/Africa also assumes responsibility for the necessary communications within Europe/Africa. In Europe, the DEO is represented by the director. Environmental and Regulatory Affairs. Other countries/regions may specify additional functions who share responsibility.--------------
1.2 Employee Communication, Education and Training Concerning the Huirds of Substances in the Workplace
All employees whose work provides potential exposure to a hazardous chemical substance will have ready access to reference material, such as a Material Safety Data Sheet (MSDS), and will receive training in the nature of the hazards and appropriate work practices, protective measures and emergency procedures. Such training yviU be provided to employees when newly assigned to an area with potentially hazardous exposures and annually thereafter.
U Employee Access to Medical and Exposure Records
Access to an employee's medical or exposure records (if generated) will be provided within IS working days after the congnny receives a request in person or in writing from that employee, or as required by law if more stringent.
In addition to individual medical and exposure records, an employee may have access to general exposure records (such as area samples) for his/her work area and the individual exposure records (with all identifiers deleted) of other employees in the same work environment Since much of the data requires interpretation or explanation, the most appropriate physician or nurse should be present during the review of medical records, and the industrial hygienist or industrial hygiene contact should be present during the review of exposure records to provide such Interpretation and consultation.
Written requests for medical and exposure records will be kept at the location housing the records.
1.4 Other Communication of Exposure Information
Employees who participate in individual (personal) industrial hygiene monitoring will be informed of the sampling results.
All employees in an area where ambient air concentrations or physical agents are monitored should be informed of area concentrations, their relationship to relevant federal, state or local permissible exposure limits, the company's guidelines, and intended corrective action where required.
United States Specific: For certain substances, OSHA regulations require written notification to the employee.
MONSANTO COMPANY
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1.5 Communication of Physical Examination and Medical Test Data to the Employee
An employee will be informed about results of health evaluations and medical tests.
Copies of medical information will be sent to private
physicians upon the employee's request and only with
written authorization.
.
United States Specific: The employee will be informed in writing about results of health evaluation performed for occupational surveillance.
1.6 Employee Inquiries
Any employee inquiry about work exposures must be addressed by site management The location physician, industrial hygienist or other appropriate management representative(s) should meet with the employee and provide a specific response based on the factual information available. The appropriate DEO, manager. Human Resources, and corporate ESH representative should be consulted in any non-routine situation.
Europe/Africa Specific: The director of DMHS Europe/Africa should be consulted in any non-routine situation in Europe/Africa.
'
1.7 Communication of Health Studies
When employees have been involved in epidemiology or
other health studies conducted by or on behalf of the
company, an executive summary of the study results
prepared by corporate ESH will be communicated in
writing to the responsible DEO and site managers.----------
Communications with the employees will be
coordinated by the corporate DEO. The DEO may ask
ESH and/or Europe Environmental and Regulatory
Affairs (ERA) staff to develop a Communications
Document and Dissemination Plan in consultation with
plant personnel. A decision will be made at that time as
to the total population to be included in the
communication.
..
Other studies known to the company which are scientifically sound and which present significant new information concerning the potential hazards of a material to workers should be communicated to employees who have potential exposure to the substance. Where possible, employees should learn about significant potential hazards of materials with which they work from the company, and not from outside sources. However, a multitude of
epidemiological, animal and other health studies are conducted annually by the company and by others. These studies vary widely in terms of new knowledge provided, scientific validity, conclusiveness of the findings, applicability to humans or the work environment, etc. Location management in consultation with the DEO and corporate ESH and DMHS Europe/Africa (for Europe/Africa sites) should communicate in writing any applicable, reliable study results.
In determining where the results of a study should be communicated, factors such as the following should be evaluated:
the scientific validity and conclusiveness of the study;
whether the study produced new results of significance;
the applicability of the study to employees;
the significance of any potential hazard identified; and
___ the plans for follow-up studies.
When there is a question of whether the results of a study are significant enough to be communicated to appropriate employees corporate-wide, the matter will be referred to the following administration by any member of concerned management: The director of Medical and Health Sciences, Industrial Hygiene director. Corporate Toxicology director. Epidemiology director. Medical director, appropriate DEO and the assistant general counsel. Environmental Law. The appropriate Directors of Manufacturing, Human Resources and Public -- - - Affairs/Relations will also provide consultation. A draft Communication Document and Dissemination Plan will be developed upon request, initially within ESH, to ensure that the study results are properly interpreted and that the communique will be properly reviewed and disseminated to all operating units and/or plants. The DEO, with support from corporate Industrial Hygiene and DMHS Europe/Africa (when Europe/Africa sites are involved) will transmit draft statements, announcements and supporting data to the appropriate location management
1.8Access to Employee Medical or Exposure Records by Designated Representatives
A designated representative with the appropriate written authorization from the employee will be provided access to an employee's medical and exposure records within 15 working days of receipt of the authorization. A
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designated representative is any individual or organization to whom the employee has given written authorization to have access to the employee's medical or exposure records for a specific purpose on a specified occasion.
United Suites Specific: OSHA rules require that an employee's recognized or certified collective bargaining agent will be treated as a designated representative without regard to written employee authorization with respect to access to employee exposure records (with all identifiers deleted) and analyses of group medical and exposure records only. Final reports of completed epidemiological studies of unionized employees will be provided to the union involved on specific written request. Information on the study results will be provided to all affected employees in a timely manner if this has not been done previously.
The appropriate managers. Human Resources and ESH representatives (DMHS Europe/Africa when Europe/Africa sites are involved) and the assistant general counsel. Environmental Law, should be advised of requests for access to records from a designated ~ representative.
An OSHA inspector who presents a written access order approved by the Assistant Secretary of Labor for OSHA will be given immediate access to records specified by the order. No order is required for access to exposure records. Requests should be reported immediately to the assistant general counsel. Environmental Law. Requests by NIOSH have been supported by the courts but should be cleared by the assistant general counsel. Environmental Law, before being granted. Reference should be made to 29 CFR Part 1910Access to Employee Exposure and Medical Records, Final Rule 929-88.
1.9 Notification to Employees of Right of Access
Each location should make such notification of the existence, location and right of access to medical and exposure records a part of its new hire orientation program and should post or otherwise inform all employees of this information and right each year.
1.10 Employee Health and Exposure Communications Plans
Each manufacturing and laboratory location should have written Employee Health and Exposure Communications Plans which address such things as those as follows:
the communication of and training on the hazards of chemical substances and physical agents in the workplace and proper handling methods, protective measures and emergency procedures:
the handling of employee inquires and expressions of concern about exposures:
the handling of employee and designated representative requests for access to medical and exposure records;
the communication of abnormal physical exam/medical test findings;
the regular communication of the industrial hygiene program and of exposure levels vs. standards;
the identification of materials or other subjects needing special communications efforts and plans for development of such programs locally or with the help of DMHS or others; and
notification to employees of their right of access to their medical and exposure records.
1.11 ESH Responsibility for Communication Programs
When its specialized expertise and/or a general communications need deem it appropriate, corporate ESH has a responsibility to develop a Communication Document and Dissemination Plan upon request for new health hazard information. The appropriate DEOs and management at representative plants will be consulted in the development of such plans to make them more suitable and effective for plant use.
'Europe/Africa Specific: Europe Environmental and Regulatory Affairs will be responsible for developing a Communication Document and Dissemination Plan which is appropriate for the laws and customs governing handling of employee health and exposure information in those countries.
1.12 Definitions
Access to Records: Consists of an opportunity to review an employee's medical and exposure records on site, and if requested, receipt of or opportunity to make a copy of the records. Unless otherwise specified by law, trade secret information may be deleted from the records provided to an employee or designated representative but they must be so informed that this was done.
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Medical Records: Include reports of physical examinations, medical tests and other medical information on the employee in the company's possession.
Exposure Records: Include records of an employee's
work history and the level of exposure to potentially
harmful or toxic substances or agents and analyses of
such records.
'
Epidemiology Studies: Defined as scientific investigations of potential relationships between workplace exposures and health outcome of company employees or other occupational populations, as outlined in a study protocol.
(Revised and Approved: Vice President, Environmental, Safety and Health, October22,1992.)
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OSH 107.973
WATER_PCB-SD0000021519
PROCEDURE
. #2
TRANSMITTAL TO THE UNITED STATES ENVIRONMENTAL PROTECTION AGENCY OF SUBSTANTIAL RISK INFORMATION UNDER THE TOXIC SUBSTANCES CONTROL ACT
The company's procedure for handling the reporting ofinformation to the United States Environmental Protection Agency (USEPA) under the 8(e) substantial risk section ofthe Tbxic Substances Control Act (TSCA) as follows:
2.1 Abstract of Requirements
TSCA Section 8(e) requires any person (company) who manufactures, processes or distributes in commerce a chemical substance or mixture and who obtains information which reasonably supports the conclusion that such substance or mixture presents a substantial risk of injury to health or the environment shall immediately inform the EPA of such information.
2.2 Who Is responsible for reporting?
The requirements of Section 8(e) of the TSCA apply to "any person who manufactures, processes, or distributes in commerce." It is the company's position that the "person" who engages in the commercial activity is only the business organization, whether a sole proprietorship, corporation, partnership or association.
2.3 How are 8(e) reporting decisions made?
Company organizations that might receive TSCA 8(e) information will have a designated individual to whom such information shall be communicated. At least annually, the director of regulatory management (DRM), Toxic Substances, will publish a list of the designated individuals.
Anyone obtaining information of the type given in the abstract of requirements and detailed by EPA in their TSCA Section 8(e) Reporting Guide, dated June, 1991, should immediately submit such information to their supervisor. The supervisor shall immediately relay the information to the location or department manager, whichever is applicable, who. in turn, transmits it to the
proper designated individual in the organization. The information is then transmitted directly to the director of Medicine and Health Sciences.
It is imperative that the flow of information through this transmittal chain be rapid. In the event of nonavailability of a member of the communication network at the time information is first obtained, such member should be bypassed in the interest of speed.
All individuals involved in submission of substantial risk information to the director of Medicine and Health Sciences should keep a record of date of receipt and pertinent identifying details.
The director of Medicine and Health Sciences: environ mental counsel: DRM. Toxic Substances: and the appropriate operating unit directors) of environmental operations will comprise the designated official 8(e) committee to make decisions with respect to information that must be reported to the EPA under Section 8(e) of the TSCA.
Appropriate senior management will be informed of committee decisions.
In the event that a committee decision is not unanimous, the next appropriate level of management shall be consulted, and the matter will be resolved at the highest level, if necessary.
Employees who submit information through company channels will be notified of action taken by the 8(e) committee together with reasons for such action.
MONSANTO COMPANY
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In the event that, after the company has evaluated information and has determined that the item Is not reportable under Section 8(e), the company becomes aware that an employee, as an individual, subsequently reported the item to the EPA, the company should review the situation to determine what action, if any. it should take with the EPA.
2.4 How are employees notified of 8(e) requirements?
All exempt company employees and others so designated by their organizational unit (plant nurses, contract physicians, scientists and engineers, etc.) within organizations that might receive or have access to TSCA 8(e) information, shall be informed of the provisions of Section 8(e). Annual reminders of 8(e) requirements will be provided to said employees. Records documenting the information communication will be maintained by the DRM, Toxic Substances.
(Revised andApproved: Vice President, Environmental Safety and Health, October 22,1992.).......
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QSW 107975
PROCEDURE
#3
RECORDING ALLEGATIONS OF SIGNIFICANT ADVERSE REACTIONS UNDER THE TOXIC SUBSTANCES CONTROL ACT
The company's procedure for handling the Recordkeeping Requirements ofthe United States Environ mental Protection Agency's (USEPA) Final Rule Under Section 8(c) ofthe Tbxic Substances ControlAct (TSCA) is as follows:
3.1 Abstract of Rule
Manufacturers and certain processors of chemical substances and mixtures must maintain records of significant adverse reactions to health or the environment alleged to have been caused by a substance, mixture, article, process, effluent or emission. These records are subject to USEPA inspection. -
Rule Reference - 40 CFR Part 717 (48 FR 38178 August 22,1983)
ii. Was a manifestation of a toxic effect after a significantly shorter exposure level than described.
iii. Was a manifestation of a toxic effect by an exposure route different from that described.
c. "Significant adverse reactions" are reactions that may indicate a substantial impairment of normal activities, or long-lasting or irreversible damage to health or the environment.
Note: The Rule does not apply to pesticides, food, food additives, drugs or cosmetics when manufactured, processed or distributed for these uses.
33 Key Definitions
- -
33 Exemptions from the Rule that Relate to the Company
a. Activities involving solely mining or other solely extractive functions.
(See Section 717.3 of the Rule for complete listing of definitions.)
b. Significant adverse reactions that are known human effects.
a. "Allegation" means a statement made without formal proof or regard for evidence, that a chemical substance or mixture has caused a significant adverse reaction to health or the environment
c. Significant adverse reactions to the environment directly attributable to incidents of environmental con tamination that have been reported to the United States federal government under any applicable authority.
b. "Known human effect? means a commonly recognized human health effect of a particular substance or mixture described in:
L Scientific articles or publications abstracted in standard reference sources.
ii. The firm's product labeling or material safety
data sheets (MSDS).
.
However, an effect is not a "known human effect" if it
i. Was a significantly more severe toxic effect than previously described. .
3.4 Who Can Receive an Allegation?
Allegations can come from a variety of sources including employees, contractors, customers and neighbors.
As a result, the company's receiving network must be broad. Initial receptors include plant, laboratory and other company location supervision, plant and other company location managers, the company's medical community at all locations, the offices of the operating company directors of Environmental Operations, sales and marketing contacts, switchboard operators at all locations, and environmental network contacts.
MONSANTO COMPANY
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3.5 Procedure for Handling Health or Environmental Allegations
The company's Toxic Substances Control Act (TSCA)
Section 8(c) procedure consists of a four-step review
and decision process. A determination than an allegation
is not recordable under the Rule can be made at any step
in the process. The procedure is shown schematically on
Appendix 3.3.2.1
.
a. Step One - Each plant or other company-designated locations or laboratory will have at least one identified and trained TSCA Section 8(c) key contact The director of Environmental Operations (DEO) or designee from the appropriate operating companies, representatives of the Business and Research Support Services (BRSS), and director, regulatory management (DRM). Toxic Substances, will serve as the key contacts for the General Office. The DEOs have responsibility under this procedure for free standing divisions and subsidiaries of which the err :pany owns 50 percent or more of the voting stock or other equity rights, or for which the company has the power to control the management and policies of that firm. At Step One, all initial receptors will automatically transfer persons making oral allegations to the key contact at their locations. Initial' receptors will also transfer written allegation to the key contact at their location. There are two exceptions with respect to oral allegations: If the initial receptors are either members of the department of Medicine and Health Sciences Occupational Medicine (DMHS-OM) group (physicians) or the DEO's office, then these individuals may judge at Step One if an oral allegation is exdoded. Decision criteria for Step One: pesticides, food, food additives, drags, or cosmetics are excluded. If a decision is made that the allegation is excluded, the allegation, if written, will be discarded and. if oral, will not be acted cm under this procedure.
If the allegation is oral and not excluded, the key contact will inform the alleger that such allegation may be recordable under the Rule and request that the alleger submit a written and signed allegation to the key contact. Monsanto Form 8(c)A. shown on Appendix 3.2, is available to be used for all employee related oral health allegations and can be used at the discretion of the DEO for external oral health allegations. All key contacts must note on a written allegation the date of its receipt
b. Step Two The key contact at a company location or the appropriate DEO for the General Office will pro vide company employees with Form 8(c)A for oral allegations of health effects. Written allegations will then be reviewed by the key contact, who will then make a Step Two decision. The key contact will deter mine if the written allegation is exempted from the Rule using the criteria in Step One. If a decision is made that an allegation is exempt from the Rule, the allegation will be discarded. Otherwise, the allegation will be sent to the appropriate DEO for review.
c. Step Three - The appropriate DEO will serve as the coordinator for Step Three and Step Four activities. Allegations received from the location (e.g. plant, etc.) key contacts will be reviewed by the DEO and a Step Three decision made. A Step Three decision will also be made by the DEO or other General Office key contact regarding allegations made to the General Office receptors. If the Step Three decision is that the allegation is not recordable under the Rule, the allegation will be discarded. Otherwise the allegation will proceed to Step Four.
d. Step Four - The DEO will form a committee to make decisions with respect to allegations that must be recorded under the Rule. The committee will be chaired by the DEO and consist of the appropriate members of DMHS-OM for human effects, appropriate members of Environmental Sciences staff for environmental effects. Environmental Law staff, and the DRM, Toxic Substances. If the decision is that the allegation is not recordable under the Rule, the allegation will be discarded. The DEO will provide feedback to the location key contact. If the Step Four decision is that the allegation is recordable under the Rule, than the DRM, Toxic Substances, will place the allegation and documents mandated by the Rule in the TSCA Section 8(c) file. The DEO will provide feedback to the location key contact
3.6 Recordkeeping
The TSCA Section 8(c) file will be kept in the Office of the DRM, Toxic Substances. The file structure will confoim to requirements of Section 717.15 of the Rule. Files pertaining to adverse reactions to health of employees will be retained for 30 years. Hies pertaining to other adverse reactions will be maintained for five years.
'A separate procedurefor litigation claims (Appendix 3.3.1) and the company's Wear-Dated Hotline (Appendix 3.3.3) will be used
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WATER_PCB-SD0000021523
3.7 Communications
a. Disposition of written allegations will be communi cated back to tbe individual making the allegation. The key contact will facilitate the communication.
b. A summary of the TSCA Section 8(c) procedure will be periodically communicated to all affected employees and updated, as appropriate.
(Revised and Approved: Vice President, Environmental, Safety and Health, October 22,1992.)
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Appendix 3.1
SIMPLIFIED FLOW DIAGRAM OF MONSANTO PROCEDURE FOR HANDLING ALLEGATIONS SUBJECT TO TSCA 8(c)
STEP ONE: Decision
Not subject to TSCA 8(c) recordkeeping. Drop from process.
Note: Initial Receptors may be key contact. DEO office is also a key contact.
STEP FOUR: ---------Decision
Allegation qualifies for TSCA 8(c) recordkeeping. Put in 8(c) Tile in St. Louis PR3, Page 4 of 8 Company Confidential
Send written allegation and Forms 8(c)A to St Louis
i
DEO Office
DEO forms an 8(c) review committee
I
8(c) Committee
OSW L0797S
STEP TWO: Decision
Not subject to TSCA 8(c) recordkeeping. Drop from process.
STEP THREE: Decision
Not subject to TSCA 8(c) recordkeeping. Drop from process.
STEP FOUR: w- Decision
Not subject to TSCA 8(c) recordkeeping. Drop from process.
WATER PCB-SD0000021525
TO: SITE KEY CONTACT
Form 8(c)A 11/92
Appendix 3.2
REPORTING FORM FOR ALLEGATIONS OF SIGNIFICANT ADVERSE REACTION TO HEALTH
Toxic Substances Control Act, Section 8(c) 40 CFR Part 717
NAME OF ALLEGER:_____ ADDRESS: (If not employee)
SITE LOCATION:
DATE:_____ /_____ /____
MO DAY
YK
SITE LOC CODE:
(If health effect only): M F
YR. OF BIRTH: _
Employer (if other than Monsanto):____ ___________________________________
DESCRIPTION OF ALLEGED AVERSE HEALTH EFFECT: 1. WHAT IS TOE HEALTH EFFECT BEING CLAIMED? _________________
2. HOW LONG DID IT LAST?
3. HOW OFTEN HAVE YOU EXPERIENCED EFFECT?
4. IN WHAT WAY DID IT AFFECT YOUR NORMAL ACTIVITIES?
5. HOW WERE YOU EXPOSED?
WHAT SUBSTANCE, MIXTURE, PROCESS OR OPERATION DO YOU THINK CAUSED TOE EFFECT YOU DESCRIBED:
FOR COMPANY USE ONLY: RECEIVED ON: B Y:
OSH 107980
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WATER PCB-SD0000021526
Appendix 33.1
TSCA 8(c) RECORDKEEPING: LITIGATION CLAIMS
Detailed Procedure:
Step 1
Litigation complaints will be reviewed at the time of receipt by the law department for relevance to TSCA 8(c) recordkeeping. Criteria for this reiriew include the following:
a) Is the claim against a Monsanto product or process? b) Is the produces) in question one that is covered by TSCA. i.e., other than pesticide, herbicide, food, food
additive or pharmaceutical? c) Is the claim a health or environmental claim?
If all criteria is met, the claim will be sent to the DMHS occupational medicine group. Exceptions to this include claims against the Agricultural Group, Nutrition and Health Care Products that will be sent to these respective groups when the law department is unsure of the answer to question (b).
Step 2
The occupational medicine group of DMHS will review the litigation claims passed to them by the law department The
review will be based on EPA's definitions of "known human effect" and "significant adverse reactions" (40 CFR 717).
For environmental effects. DMHS may need to contact the appropriate DEO for assistance. Claims that do not meet
TSCA 8(c) criteria will be dropped from further TSCA review of this step. Those claims that meet TSCA 8(c) criteria
will be forwarded to the DRM, Toxic Substances, for filing.
-
Sup 3
Claims meeting the 8(c) criteria will be filed in the TSCA 8(c) file maintained by the DRM, Toxic Substances. This office will request a copy of the complaint, abstract, and "answer" from the law department.
Step 4
The law department will forward a copy of the complaint, abstract, and "answer" to the DRM, Toxic Substances, for filing in the TSCA 8(c) file, along with the "complaint." The "complaint," abstract and "answer" will constitute the TSCA 8(c) recordable "allegation" and "follow-up" for all litigation filings.
A block flow diagram of the TSCA 8(c) process for litigation complaints appears on the reverse side of this page.
(Revised 10/22/92)
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OSH 107981
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Appendix 3.3.2
TSCA 8(c) REVIEW PROCEDURE OF LITIGATION CLAIMS
Request "Answer"
t
Law Department
"Answer" I
OSH 107982
DRM TSCA
FUe "Answer" In 8(c) nie
PR3. Page 7 of 8 Company Confidential
WATER PCB-SD0000021528
Appendix 3.3.3
TSCA 8(c) RECORDKEEPING: WEAR-DATED HOTLINE
Detailed Procedure:
Step I
AH health and environmental effect allegations received by the Wear-Dated hotline will be documented by the
phone operator on a standard fotta.
'
Step 2 The documented health and environmental effect hotline call will be reviewed by the Chemical Group Product Safety department for TSCA 8(c) relevance.
Step 3 The hotline allegations that are judged by the Chemical Group Product Safety department as meeting TSCA 8(c) recordkeeping requirements will be forwarded to the DRM, Toxic Substances, for filing.
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OSH 107983
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PROCEDURE
#4
PREMANUFACTURE NOTIFICATION TO UNITED STATES ENVIRONMENTAL PROTECTION AGENCY UNDER THE TOXIC
SUBSTANCES CONTROL ACT
The company's procedure for development ofpremanufacture notification (PMN) to the United States Environmental Protection Agency (USEPA) as required under Section 5 ofthe Tbxic Substances Control Act (TSCA) is as follows:
4.1 Abstract of Requirements
A PMN is required to be submitted to USEPA for all new chemical substances at least 90 day before the substance can be manufactured for commercial purposes. A number of substances are exempted from these requirements, including, but not limited to drugs, food and food additives, pesticides, RAD substances, nonisolated intermediates, and substances on the TSCA inventory.
Final Rules Reference - 40 CFR Part 720.
4.2 Isa PMN Required?
At a very early stage of new product development, including isolated intermediates and new imports, several checks should be made to determine if a PMN will be required for the product
4.2.1 Is the Product (Substance) Exempt under TSCA?
Responsibility: Operating unit director. _ Environmental Operations (DEO) or designee.
Section 2(B) of TSCA exempts broad classes of substances such as pesticides, food, food additives, mixtures and others.
The PMN rule exempts small quantities for RAD purposes and has provisions to exempt substances for test marketing low volume manufacture and for polymer manufacture.
The rule also exempts impurities, some by-products, articles and nonisolated intermediates.
Refer to TSCA law and regulations or the company's PMN manual for details or contact operating unit DEO or designee or director, regulatory management (DRM). Toxic Substances (TSCA).
4.2.2 Is the Substance "New" under TSCA? (Is It on the TSCA Inventory of Chemical in Commerce?)
Responsibility: Operating Unit DEO or designee.
Contact the operating unit DEO or designee and have the TSCA non-confidential inventory searched for the substance.
If the substance is on the TSCA nonconfidential inventory, it is not new under TSCA definition and a PMN is not required. If the substance in question is not on the nonconfidential inventory, the confidential inventory must be searched.
To search the confidential inventory, a Bona Fide Intent to Manufacture (BIM) notice must be submitted to USEPA. A copy of the instruction for submitting a BIM can be found in 720.25 of 40 CFR 720. Send a copy of the BIM to the DRM. TSCA, for corporate recordkeeping purposes.
MONSANTO COMPANY
O S to 10#
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WATER_PCB-SD0000021530
If USEPA reports that the substance is not on the confidential inventory, then the substance is a new substance under TSCA and a PMN is required unless the material is exempt under Section 2 (a) above.
4 j What Information Is Required on a PMN
Submission?
Final rules detailing the PMN requirements can be found in 40 CFR 720. All PMNs must be submitted on USEPA Form 7710-25 (1/91). Copies of the form and instructions for its use are available from the DRM, TSCA. The required PMN information falls into either the category of General Information or Risk Assessment Data. USEPA will accept additional data- in many cases, it is desirable to submit Risk Analysis, pollution prevention data or other information to assist USEPA with their assessment. Since the company performs a Risk Analysis on all new products via the Pledge Guidelines and the EC-201/202 procedures, the information is available for this purpose.
4.4 What Are the Details of the PMN Procedure?
The PMN process should be integrated into the
.
development scheme of a new project In most cases, the
PMN development will be initiated during the earliest
phases of commercialization of a product The PMN
must be submitted to USEPA at least 90 days before the
product can be manufactured for commercial purposes,
including test marketing.
4.5 How Is a PMN Initiated?
Responsibility: Operating unit DEO or designee.
The operating unit contact submits an ER-200 or EC-201 to the Department of Medicine and Health Science (DMHS) if one has not already been submitted (See company booklet G-2738 for ER-200 and EC-201/202 Procedures).
The operating unit contact drafts a PMN using the USEPA form.
The operating unit contact calls a scoping meeting. Minimum participants at the meeting are operating unit contact, operating unit DEO or designee (if not serving as a contact), member of corporate Environmental Sciences center or other qualified environmental effects expert (if appropriate), DMHS toxicologist and DRM, TSCA. Copies of PMN drafts, along with an
PR4. Pape 2 of 3
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approved ER-200 or EC-201 for the substance are supplied to participants in advance. Note: The scoping meeting can be bypassed at the discretion of the operating unit DEO. At the scoping meeting, decisions are made by the operating unit contact, as to the scope and detail of optional information to supply. If optional risk analysis is desired, assignments are made to DMHS toxicology, industrial hygiene, etc., to complete the necessary sections. A decision is also made as to whether an EC-202 is needed before a PMN submission. Note: It is appropriate at this stage ofproduct development to initiate a Material Safety Data Sheet (MSDS) and a TF-837for label andfreight classification.
4.6 How Are PMNs Finalized? Responsibility: Operating unit DEO or other designated operating unit contact. The operating unit contact prepares a final draft using input from the scoping meeting as well as follow-up input from DMHS. The operating unit contact, together with the patent department, reviews the final draft for confidential information and develops appropriate confidentiality claims with substantiation, where necessary. The final draft is circulated to the participants of the scoping meeting for final review. The operating unit contact calls a meeting for final comments/approvals if needed.
4.7 How Are PMNs Submitted?
Responsibility: DRM, TSCA After final review/approval, (he operating unit
contact forwards the PMN to the DRM, TSCA (authorized official), for submission. The DRM, TSCA, will submit the PMN (both confidential and non-confidential as appropriate), using applicable USEPA submission requirements.
i079a5
WATER_PCB-SD0000021531
4.8 How Is USEPA Follow-up on i PMN Handled?
Each PMN will identify a technical contact in addition to an authorized official. The technical contact will typically be operating unit DEO. Commercial Develop ment, or R&D contact
4.8.1 PMN Fees
A S2.500 fee is required for all PMNs, except intermediates filed at the same time
as final product (SI,000) or exemptions
(zero cost).
A unique six-digit TS-user fee identification must be assigned to each PMN and must also appear on the check.
The fee is sent to a separate USEPA office from the PMN.
4JL2 Phone Contact
All calls from the USEPA on technical matters should be handled by the "Technical Contact."
All verbal questions concerning nonconfidential inquiries by the USEPA may be discussed at the time of call or deferred to obtain an answer if unknown or if unsure as to USEPA authority to ask for the information.
Non-confidential oral responses may be followed up with a written response when deemed appropriate by the contact. In all cases the technical contact should write a note to file documenting the conversations, with a copy to the DRM, TSCA.
Confidential inquiries previously discussed with the USEPA or claimed confidential in the PMN may de discussed at the discretion of the technical contact
All other verbal confidential questions will be addressed by written response only.
Verba] response to USEPA will be followed up. at the discretion of the technical contact, with a written letter documenting the conversation and clearly indicating areas of confidentiality, with a copy to the DRM, TSCA.
4iJ EPA Actions
.
Responsibility: The operating unit DEO or
designee will have prime
responsibility, with counsel
of Environmental Law and
the DRM, TSCA.
USEPA may extend the review period by an additional 90 days.
USEPA may ask for more information under Section 5(e).
i. An order may be issued by USEPA.
ii. A consent order may be jointly agreed upon. The consent order can include restriction on manufacture or use in lieu of information generation.
USEPA may restrict manufacture or use under Section 5(f).
4.9. How Is the Company Follow-up on the PMN Submission Handled?
Responsibility: Operating unit DEO or designee.
The company may request USEPA to stop the clock on PMN reviews at any time during the review period.
After USEPA's review period expires, manufacture can commence at any time, subject to any 5(e) or 5(0 restrictions. A Notice ofCommence to Manufacture (NCM) must be submitted to USEPA within 30 days of the first manufacture for commercial purposes. The information to be included in the notice are detailed in 40 CFR 720. Confidential claims must be made again at this time, as appropriate. Send a copy of the NCM to the DRM, TSCA for corporate recordkeeping purposes. Once a NCM is filed with USEPA, the PMN substance is placed on the TSCA inventory.
(Revised and Approved: Vice President, Environmental Safety and Health. October 22.1992.)
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PROCEDURE
#5
OCCUPATIONAL FATAL ACCIDENT REPORTING
In case ofa fatal accident, the company's Law Department must be contacted in addition to following government, operating company, and corporate-reporting requirements.
OSHA regulations require that, within 48 hours after the occurrence of an employment accident which is fatal to one or more employees or which results in hospitaliza- . tion of five or more employees, the employer of such employee(s) shall report the accident either orally or in writing to the nearest office of the OSHA Area Director. The reporting may be by telephone or telegraph. The report shall relate the circumstances of the accident, the number of fatalities, and the extent of any injuries.
In such instances the following guidelines are considered necessary to protect the civil rights of company employees.
In addition to routine operating company and corporate notifications in fatal accidents, either Mary M. Tonkin or Michael E. Gewin (for accidental deaths) or L. William Higley (for deaths for long-term chemical exposure), the company's attorneys for OSHA matters, must be notified immediately. The telephone numbers are listed below. They will provide prompt necessary legal guidance including, where necessary, sending an attorney to the site for on-the-spot counseling.
In the meantime, OSHA inspectors) should be given access to the site of the accident when the inspector arrives on the premises, without requiring that the inspector secure a warrant for entry. However, neither members of location management nor any wage employee should discuss the accident with the OSHA inspector until advised to do so by the company attorney.
The location manager or his designee will greet the inspector and state that location employees have been asked not to discuss the accident until the company attorney advises them accordingly.
The inspector is to be told that we have been forced to take this posture as a result of the OSHA Procedurefor Investigating Criminal/Willfitl Violations. The inspector will be permitted to inspect the plant, and, of course, should be advised of any chemical hazards and protective measures needed, related or not to the accident
Location personnel will not allow the inspector to view any records or documents at this time, other than the lost-time injury log, OSHA Form 200 and Form 101 or its equivalent, until advised to do so by the company attorney.
If the location is requested to rope off the area of the accident, local discretion should be exercised. The inspector, however, is not authorized to keep plant management away from any part of the operation.
If local management believes entry by the inspector must be delayed for a few hours because of exposure, safety, confusion, etc., management will seek such a recommendation from Ms. Tonkin or Mr. Higley at the time of the initial call to St. Louis.
Contacts Mary M. Tonkin, 314/694-2967 (office), (314) 721-8209 (home).
Michael E. Gewin, 314/694-2849 (office), (314) 352-2176 (home).
L. William Higley. 314/694-8503 (office); (314) 862-1796 (home).
(Revised and Approved: Vice President, Environmental, Safety and Health, October 22,1992.)
MONSANTO COMPANY
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PROCEDURE
#6
TRANSMITTAL OF TOXICOLOGY AND HEALTH-RELATED DATA TO UNITED STATES REGULATORY AGENCIES
Health-related information should be submitted through the Department ofMedicine and Health
Sciences.
The various regulatory agencies are continually supplied
information from toxicology and health-related tests on
the company's products done by or for die company. In
order to provide consistency in the handling and review
of such information, as well as to assure proper follow-
through on commitments to these agencies, the
transmittal of such test results will be carried out in
accordance with the following guidelines:
.
6.1 All toxicology or health-related data will be reviewed with the department of Medicine and Health Sciences (DMHS) prior to submission to any regulatory agency, except for routine submissions by the company's Agricultural Group of test data required under the Federal Insecticide, Fungicide, and Rodentidde Act (FIFRA). In addition, DMHS will be informed of all such submissions at the time via the letter of transmittal.
6.2 Any such information transmitted must be recorded and the copy of the final submission retained both by DMHS and the involved operating company.
6J The letter of transmittal for any toxicology or health-related data must include a listing of the materials being transmitted including sufficient bibliographic information for subsequent retrieval of the original data.
6.4 If the submission includes data on human health effects, it is preferable that the information be submitted to the regulatory agency by the director of the depart ment of Medicine and Health Sciences.
6.5 Agreements with a regulatory agency that commit the company to the future transmittal of toxicology or health-related data must also be reviewed and approved in advance by DMHS; further. DMHS must concur with the feasibility of meeting commitment dates. Appropriate records of such commitments must be maintained both by the involved operating company and DMHS in order to ensure future compliance with such agreements.
6.6 Any exceptions to the above must be approved by the director of DMHS.
(Revised and Approved: Vice President, Environmental, Safety and Health, October 22,1992.)
MONSANTO COMPANY
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REFERENCE: Cross Reference ESH Worldwide Guidelines, Pledge Guidelines, and Responsible Care
ESH Worldwide Guideline
Effluent and Emission Control Waste Management Plant Environmental Assessments
Employee and Community Safety and Health
Pledge Guideline Pollution Prevention
Responsible Care
Code on Pollution Prevention Practices No. 1 through No. 11, except No. 4 and No. 8
Employee And Community Safety and Health
Code on Process Safety, Employee Safety and Health and Community Awareness and Emergency Response
None (Internal Process Safety
and Emergency Response Policy Elements)
Product Stewardship
Process Safety and Emergency Response
Product Stewardship
Code on Process Safety Code on Community Awareness and
Emergency Response
Code on Product Stewardship
None (Internal Distribution Policy
Elements)
Waste Management - Corrective and Remedial Action
Plant Environmental Assessments
Chemical Distribution
Groundwater and Soil Quality
Outside Processors
*
Outside Processors
Code on Distribution
Code on Pollution Prevention, Practices No. 13 and No. 14
Code on Pollution Prevention, Practices No. 12
Code on Pollution Prevention, Practices No. 12
None
(Internal Policy Elements on Public Participation and Involvement)
Community Awareness at Manufacturing Sites
Code on Community Awareness and Emergency Response. Practices No. A1 - No. A9
Code on Pollution Prevention Practices No. 4 and No. 8
DSW 107989
REFERENCE
Company Confidential
WATER PCB-SD0000021535
Responsible Care: A Public Commitment
GUIDING PRINCIPLES
Member companies at the Chemicei Manufacturers Association are committed to support a continuing effort to improve the industry's responsible management of chemicals. They pledge to manage their businesses according to these principles:
To recognize and respond to community concerns about chemicals and our operations. To develop and produce chemicals that can be manufactured, transported, used, and disposed of safely. To make health, safety and environment considerations a priority in our planning for all existing and new products and processes. To report promptly to officials, employees, customers and the public, information on chemicalrelated health or environmental hazards and to recommend protective measures. To counsel customers on the safe use. transportation and disposal of chemical products. Tp operate our plants and facilities in a manner that protects the environment and the health and safety of our employees and the public. To extend knowledge by conducting or supporting research on the health, safety and environmen tal effects of our products, processes and waste materials. To work with others to resolve problems created by past handling and disposal of hazardous substances. To participate with government and others in creating responsible laws, regulations and standards to safeguard the community, workplace and environment To promote the principles and practices of Responsible Care* by sharing experiences and offering assistance to others who produce, handle, use. transport or dispose of chemicals.
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Responsible Care:A Public Commitment
SUMMARY DESCRIPTION RESPONSIBLE CARE* PROGRAM ELEMENTS
The statement of Guiding Principles for Resoonsi&le Care1 is a commitment ov eacn memoer company to fully support a continuous effort to improve the industry's-responsible manage ment of cnemicais Each member company has pledged to operate according to tne Guiding Principles and has signed to that effect. The signed statement is considered an obligation of membership m the Chemical Manufacturers' Association (CMA). The Guiding Principles are based on CMA's 1983 policy statement on health, safety and the environment and on the Canadian Responsible Care4 principles. They also incorporate guidance received from memoer company executive contacts.
Following association adoption of the Guiding Principles, various CMA committees began developing-Codes of Menage* ment Practices m January 1989. Each Code of Management Practices addresses several public concerns. Impetus for developing a specific Code comes from either a substantial public concern!si identified by the Public Advisory Panel or the industry, a substantive need to take voluntary action, or both. Codes m development address community awareness and emergency response, distribution, pollution prevention, process safety, employee health and safety, and product stewardship. The Codes of Management Practices identify expected manage ment practices as obiectives rather than prescribing absolute or quantitative standards. Since the Codes are intended to serve as objectives, they complement existing member company programs or practices that achieve the same goals. Responsible Care*, therefore, becomes an integral part of existing company programs and will cause each company to stretch to contmualiy
improve performance Another important element in the Responsible Care*
initiative is the Public Advisory Panel which is composed of a group of environmental, health and safety thought leaders. The panel is an industry (CMAI effort, not a company responsibility, it was assembled and is moderated by an experienced facilitator working at the association's direction. It serves to assist the industry in identifying and developing programs and actions that are responsive, and are viewed as responsive, to public con cerns. Meeting several times a year, the panel reviews issues on which CMA requires comment and advice. Panel members also identify areas they believe require.industry response, critique all proposed Codes of Management Practices and provide early definition of public concerns involving the chemical induspY- Community Advisory Panels at the local or regional level can sene companies and the industry in a similar manner CMA has developed guidance to facilitate companies formation and operation of local panels.
Effective performance evaluation is a critical element of Responsible Care* Therefore each Code of Management Practices includes a Self-Evaluation Form that measures a company s improveo use of tne management practices that the Code aefmes Memoer companies will conauct self-evaluations
for each Code annually CMA will compile tne results arc periodically report industry s collective impiementauoa orcoress to the public.
To document progress m ways that are meaningful to me public,CMA also will monitor statistical rrena aata wnere available, on industry performance. For examoie. Suoenunc Section 313 emissions reporting and Department of Transoc.ation hazardous materials incident statistics will be a component of public reporting for the Pollution Prevention Code ana tne Distribution Code.
Due to their varying size and operations, member comoanies will not be expected to be at the same level of performance for each Code of Management Practices at the same time However, it is expected that each member compaay report continued progress.
To facilitate and support each member company's continual improvement in the responsible management of chemicals. Executive Leadership Groups (ELGsl have formed ELGs provide an opportunity for corporate leaders to discuss progress and share experiences with implementing elements of Responsible Care*. These regional groups of ten to twenty executive contracts will meet at least once a year to review Codes of Management Practices under development discuss members' progress with implementing existing Codes, identify areas where individual companies need assistance from CMA or other companies, and to address other priority industry issues
Endorsement of the Responsible Care* initiative is an Obligation of Membership in the association. A member company's obligation to Responsible Care* applies to all of its chemical business. Each member company is expected to make a commitment to Responsible Care* by: a) signing the Guiding Principles of Responsible Care*' bj communicating the commitment to Responsible Care* to
employees: c) making good-faith efforts to implement the Codes of Management Practices, participate in the self-evaluation process, and meet the expectations of the Responsible Care* initiative: and d) using the Responsible Care* name and logo according to CMA's guidelines.
Member companies are also expected to participate m the development of the Codes and programs.
In an extreme case, where a member company has consis tently not conducted its operations in accordance with the Guiding Principles and program elements of Responsible Care? association representatives will meet with the member company's executive contact to seek the company's positive involvement in the program. If this fails to produce a commit ment to pursue the objectives of Responsible Care*, appropriate actions will be taken including the disassociation of me company from memOership.
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Responsible Care:1 A Public Commitment
QUESTIONS AND ANSWERS ABOUT RESPONSIBLE CARP
Q Who had the idea for the Responsible Care* initiative?
A. Executives of the Canadian Chemical Producers Association (CCPAl began Developing the concept m 1984. Executives of Chemical Manufacturers Association ICMAI member companies that have Canadian operations brought Responsible Care* to CMA's attention. CMA considered a variety of options and adopted the performance-based Responsible Care* initiative in 1988.
0 How is Responsible Core1 different from what the chemical industry has been doing?
A. Many chemical companies have programs that are designed to improve performance. However. Responsible Care* is a broad chemical industry commitment to improve performance through a process that ensures responsiveness to the public's concerns. Two aspects make Responsible Care* unique. First bylaws obligate CMA member companies, representing 90% of basic industrial production capacity in the United States, to participate in the initiative. And second, through a Public Advisory Panel, the public is directly involved in developing program elements.
Current CMA programs such as Community Awareness and Emergency Response ICAER). Air Quality. Waste Minimization, and National Chemical Response and Information Center (NCRIC) are vital parts of the initiative. Through Responsible Care' s self-evaluation process and Public Advisory Panel. CMA will identify areas where additional resources need to be developed to help member companies achieve the goals of the initiative. Responsible Care* also encourages member companies to help each other improve performance by sharing expenences and resources in specific areas of chemical operations.
Q Why does the chemical iadestry seed to do anything?
A. Because in spite of past efforts there still are too many incidents involving chemical operations. Politicians and government regulators will respond to the public's concerns about chemicals ancfour industry if the chemical industry does not respond first Therefore, it is important for the industry to take continuing positive action to address public concerns.
Q Isn't there some other way? The cbemicel industry is already doing e let can't it just communicate this?
A. The CMA membership concluded that the chemical industry doesn't just have a public relations problem: it has a perfor mance problem. The chemical industry has to respond effectively to public concerns through improved performance. It is clear mat me public's expectations are not being met on a
performance basis. Until me chemical industry truiv understands puoiic concerns and addresses mem for a oerfcrmance standpoint. CMA member companies can t oossiow improve the public perception of their industry
Q Who proporod tfco Guiding Principles and what are they based oo?
A. The guiding Principles are based on CMA's 1983 boardapproved policy on 'Health. Safety and the Environment' and the Canadian Responsible Care* principles. They are consistent with both. They were prepared by representatives of CMA member companies and approved by the CMA Board of Directors.
Q Why does CMA's Board think Responsible Care * will work?
A. Since Responsible Care* is based on concepts proven m bom the Canadian experience aod CMA's voluntary programs such as CAER. the CMA membership has confidence that it can achieve improved industry performance. Most important by signing me Guiding Principles. CMA member companies have demonstrated their commitment to make' Responsible Care* work.
Q How much will Responsible Cere* cost CMA member companies to implement?
A. Significant resources are needed from member companies, both in terms of the `sweat equity' of participants in the development and support of the program, and in the people and dollars necessary to make the initiative `live* In each company.
These costs have not been quantified because they will be different for each company. However, overall industry costs for Responsible Care* implementation will undoubtedly add to the billions of dollars already being spent by industry to manage health, safety, and environmental issues.
Q Why should a commitinent to Rospoosiblo Cora* bo an obligation of momborship?
A. Public concerns about chemicals and the industry are the result of collective experience with the entire industry. If the chemical industry is to respond to public concerns effectively, it must act as a total industry: Responsible Care* must be visibly working throughout the industry and. therefore, must be both a commitment and a membership obligation of every company in the association, ft is critical to achieve the cultural change needed for. the industry to improve performance in a responsive manner. The public must be convinced that the chemical industry is living up to its commitment.
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Q Why have a Public Advisory Panel?
A. Rescinding to ouoiic concerns is what Resoonsibie Care' <s
all aoout Therefore, a xev component of tne initiative is rne
Puonc Aovisorv Panel Tne oanei neios the industry loentifv and
oeveioo orograms and actions that are resoonsive to public
concs'ns aocut soecnic oerformance.orooiems.
CMA nas aiso ceveiooec a gumebook for companies which
wish to estaonsn community advisory panels at operating
locations
'
q who is on the Public Advisory Panel? Who sets it up? Can panel members be replaced.
A. The Public Advisory Panel acts as a sounding board for public
concerns ana as a specially Qualified focus group that directly
imoacts industry policies and programs under Responsible Care*
Meeting five times a year, oanei members help CMA identify Puoic concerns and suggest ways to respond to those concerns.
Panel members aiso review proposed Codes bf Management
Practices and evaluate other features of the initiative. Each
meeting is managed by an outside facilitator experienced with
panel management, industry representation is kept to a
minimum to encourage an open exchange of views and ideas.
Currently, me panel is a 15-member group composed of
individuals from bom public and private sectors. To ensure that
a wipe range of public opinion is expressed, the composition of the panel is diverse, Occupations and interests of members
range from business and local government officials to environ
mental. academic, and consumer activists, a fanner, and an
expert in business ethics.
'
Panel members were selected by the facilitator. Panel
membership will penodically change in response to pane) members' availability and/orthe changing needs of penei
expertise. The facilitator will handle such changes.
Q Who wiH develop the Cedes of Management Practices? Will the public have imput?
A. The development of Codes of Management Practices begins with me identification of public concerns by a number of sources, including the Public Advisory Panel and-CMA's Board of Directors. CMA reviewsthese concerns and recommends priorities for Code development If a public concern cuts across a range of company operations or activities, it maybe addressed by more than one Code.
CMA member comoany experts develop each Code. Every memoer company has opportunities to comment on the Codes through open meetings and workshops. Public input to the codes is achieved through the Public Advisory Panel. All codes, once approved by CMA's Board of Directors; are made available to others. Use of the Responsible Care* service mark, however, must follow CMA's guidelines and can be used only with CMA approval.
0 Will Responsible Cara* Codes of Management Practices become the basis for future legislation and fegulation?
A. A very positive result of Responsible Care* should be for its meaningful and workable practices to be reflected in legislation or regulation that the public endorses through government action.
Q How will performance against the practice Codes be measured? Who does the measuring and how are the results reported?
A. 'naiviauai comoany managemerr wim 5v3n,c!f :~z
performance agamst the Cooes of Manacemer; =-j::
annually bv fiimc out a seit-evaiuauon :::r. -or ear Z:zs
Companies will feed this information cacx rc CMA s- me", r;
of such feedback would De to direct tne association $ sue::"
work to areas of tne greatest neeo ana highest ootent.a Cvr
me longer term, these aggregate reoons sncuic =s:a:-s* a
record of improvenvenrtnarwitt enaole CMA
------
industry's performance progress to the puonc
0 What will CMA do to holp companies address the Codes of Management Practices?
A. CMA will develop support programs to help companies implement the practices defined m the Codes in genera*, programs and aids (videotapes, guide-books, educational meetings, etc.) will be similar to the support provideo tor Tme ;i: and CAER. A unique element of Responsible Care* is trust member companies will help each other by sharing resources and methods they develop to implement the Codes of. Management Practices.
0 Given tire kind of date wo are reporting under Title III. will the public accopttho Responsible Care4 initiative now?
A. Disclosures under Tide III raise the level of public concern significantly in some cases. But their only effective response is to deal with the concerns through company and industry-wide improvements. This is the essence of Responsible Care * The experience in Canada and in the United States suggests it can work.
G Will chemical companies apply the initiative outside the United States?
A. CMA represents North American manufacturers and can best assist its members in implementing Responsible Care* here. However, the initiative is already international in scope. CMA learned from a two-year old Canadian effort Other countries that have officially adopted Responsible Care* initiatives include Australia. New Zealand. England. Germany. The Netherlands, and France.
CMA's experience with CAER suggests that good initiatives soread rapidly. The United Nations, with U.S. chemical industry assistance, has already developed an international emergency response program modeled on CAER.
CMA has shared Responsible Care* materials with counter part organizations in Europe. Japan. Australia, and Taiwan.
Page 6 of 98
OSW L07995
WATER_PCB-SD0000021541
Responsible Care: A Public Commitment
COMMUNITY AWARENESS AND EMERGENCY RESPONSE CODE OF MANAGEMENT PRACTICES
Purpose:
Hie goal of the Community Awareness and Emergency Response (CAER) Code ofManagement Practices is to assure emergency preparedness and to foster communityright-to-know. Itdemands a commitmenttoopenness and community dialogue, The code has two major components: first, to assure that member facilities that manufacture, process, use, distribute orstorehazardous materials initiate and maintain a community outreach program to openly communicate relevant, useful information responsive to the public's questions and concerns about safety, health, and the environment; second, to help protect employees and communities by assuring that each facility has an emergency response program to respond rapidly and effectively to emergencies.
The community outreach component will communicate program activities and performance under all codes of management practices and will promote an open, ongoing dialogue with employees and the community. Information should be provided about such activities as waste minimisation, emission reduction, health effects of chemicals, and efforts to ensure the safe transport ofchemicals.
The CAER Code of Management Practices is supported fay, and will build on, CMA's CAER process. CAER supports the community's right to know about chemical industry operations and their effect on safety, health, and the environment. CAER originally was a voluntary initiative focused on emergency response issues. The new CAER Code ofManagement Practices broadens the facility-community dialogue to cover the full range of safety, health and environmental issues.
Relationship to Guiding Principles
The Code helps achieve.several of the Responsible Care Guiding Principles:
To recognize and respond to community concerns about chemicals and our operations.
To report promptly to officials, employees, customers, and the public, information on chemical-related health or environmental hazards and recommend protective measures.
To participate with government and others in creating responsible laws, regulations, and standards to safeguard the community, workplace and environment.
To promote the principles and practices of Responsible Care by sharing experiences and offering assistance to others who produce, handle, use, transport, or dispose of chemicals.
. OSH 107996 R, Page 7 of 98
WATER_PCB-SD0000021542
CAER Code of Management PrmcUccs
November 6. 1989 -- Page 2
Manageimfllt Pprtices: A. Community Awareness and Outreach
Member facilities that manufacture, process, use, distribute or store hazardous materials shall have a community outreach program that includes:
Vnr Rmnloveesr
------------------
-------------- -----------
L An ongoing assessment of employee questions and concerns about the facility.
2. Communications trainingfor key facility and company personnel who communicate with employees and the public concerning safety, health, and environmental issues.
3. Education of employees about the facility's emergency response plan and safety, health, and environmental programs.
4. An ongoing dialogue with employees to respond to their questions and concerns and involve them in community outreach efforts.
5. A regular evaluation ofthe effectiveness ofdie ongoing employee communications efforts.
Far Community:
.
6. An ongoing assessment of community questions and concerns about the facility.
7. An outreach program to educate responders, government officials, the media, other businesses and the community about the facility's emergency response program and risks to the community associated with the facility.
6. A continuing dialogue with local citizens to respond to questions and concerns about safety, health, and the environment, and to address other issues ofinterest to the community.
9. A policy ofopenness that provides convenient ways for interested persons to become familiar with the facility, its operations, and products, andits effortsto protect safety,health, and the environment.
10. A regular evaluation ofthe effectiveness of the ongoing community communications efforts.
B. Emergency Response and Preparedness
'
Member facilities that manufacture, process, use, distribute or store hazardous materials shall have an emergency response program that includes:
L An ongoing assessment of potential risks to employees and local communities resulting from accidents or other emergencies.
2. A current, written facility emergency response plan which address, among other things, communi cations and the recovery needs of the community after an emergency.
Page 8 of 98
DSM 107997
WATER_PCB-SD0000021543
CAER Code of Management Practices November 6. 1989 -- Page 3
3. An ongoing training program for thoae employee* who have response or communications responsi biiities in the event of an emergency.
4. Emergency exercises, at least annually, to test operability of the written emergency response plan.
5. Communication of relevant and useful emergency response planning information to the Local _____ Emergency Planning Committee.
6. Facility tours for emergency responders to promote emergency preparedness and to provide current knowledge of facility operations.
7. Coordination of the written facility emergency response plan with the comprehensive community emergency response plan and otherfacilities. Ifno plan exists, the facility should initiate community efforts to create a plan. .
8. Participation in the community emergency response planning process to develop and periodically test the comprehensive community emergency response plan developed by the Local Emergency Planning Committee.
9. Sharing ofinformation and experience relating to emergency response planning, exercises, and the handling of incidents with other facilities in the community.
MEMBER SELF-EVALUATION
Each member company shall report
to CMA, orits designated agent, the stage ofimplementation
of each Management Practice in this Code. The reports shall be on the member self-evaluation form
attached as Exhibit A.
DSW 107997.01
R. Page 9 of 98
WATER_PCB-SD0000021544
R. Page 10 of 98
OSW 107998
WATER PCB-SD0000021545
Member Self-Evaluation January 6. 1992 -- Page 1
Responsible Care: A Public Gommitment-
CHEMICAL MANUFACTURERS ASSOCIATION MEMBER SELF-EVALUATION FORM
COMMUNITY AWARENESS AND EMERGENCY RESPONSE CODE OF MANAGEMENT PRACTICES
Member Company Name:___________ Responsible Care Coordinator Name: - - . - . - --
Address:
Telephone ( )_________________ Number qf facilities subject to code
OSH 107993 R. Page 11 of 98
WATER_PCB-SD0000021546
Member Seif-Evaluation January 8. 1992 Page 2
COMMUNITY AWARENESS AND EMERGENCY RESPONSE CODE OF MANAGEMENT PRACTICES
s4.
Inetnirtinns:
Underthe'Responsible Care Initiativeresebmeiaber .company ..will submit a Self-Evaltiatjon form
annually to CMA. To establish the industry baseline, each member company should complete this Self
Evaluation form,
`
2. Indicate on the cover page the number ofmember company facilities subject to the Code. Each company must report the mplwwmtiti^n category for all facilities subject to the Code on this form.
3. For each Management Practice on the following four pages, indicate the number of facilities that have attained each implementation category. Each facility should appear in only one milestone category per Management Practice. The total number of facilities subject to the Code should equal the number of
. facilities across all sis implementation categories for each Management Practice.
4. Only subject facilities owned or operated as of the reporting date should be included.
6. The implementation categories are:
Category NA Category EV -
Category OP Category IA
Category PP Category RI -
No action. Ifno action taken becaoee the management practice is not applicable, please explain. Evaluating existing company practices against the Management Practice.
Developing plan to implement Management Practice.
Implementing action plan Management Practice in place. Reassessing Management Practice implementation.
R. Page 12 of 98
DSW 107999.01
WATER_PCB-SD0000021547
CAER Code of Managanent Practices January 8. 1992 -- Page 3
yanaocrngnt Practices
Cltrgnrifs
Community Awtreneii
NA EV DP LA PP RI
1. An ongoing assessment of employee concerns and questions about the facility.
Comments on Category NA:-------------- --------------------- .
2. Communications training for key facility and company person
nel who will communicate with employees and the public con cerning safety, health and environmental issues.
Comments on Category NA;
3. Education ofemployees about the facility's emergency response plan and safety, health, and environmental programs.
Comments on Category NA:
_________________
4. An ongoing dialogue with employees to respond to their ques tions and concerns and to involve them in community outreach efforts.
Comments on Category NA:
5. Aregular evaluation ofthe effectiveness ofthe ongoing employee communications efforts.
Comments on Category NA:
CiU|7 NA
cutfwrtv
CatifiyPP CatagecylA
c*mrir CunogB
ItoMdaBi (hi
EwlaaUf Stn| wapay yuBm i|lMt tfca
OtnlqtalflMUlBpliMtl
'
ICtaagaMBt Practice ta pice*,
aiming
Practice
11# ffppHffffklfff plffffff# Practice.
OSW 108000
R. Page 13 of 98
WATER_PCB-SD0000021548
CAER Code of Management Practices January 8. 1992 -- Page 4
Caicgntirs
NA EV DP 1A PP RI
6. An ongoing assessment of community questions and concerns
about the facility. Comments on Category NA;.
Mfc
7. An outreach program to educate responders, government offi cials, the media, other business, and the community about the facility's emergency response program and risks to the commu nity associated with the facility.
Comments on Category NA;
8. A continuing dialogue with local citizens to respond to questions and concerns about safety, health, and the environment, and to address other issues of interest to the community.
Comments on Category NA;
9. A policy of openness that provides convenient ways for inter ested persons to become familiar with the facility, its operations, and products, and its efforts to protect safety, health, and the environment.
Comments on Category NA_\
10. A regular evaluation ofthe effectiveness ofthe ongoing commu nity communications efforts^
Comments on Category NA:;
CtUfy KA Catfry CT Caffary DP CalagaryU Category PP Catagoty XI
Maaagamaat PnctSea la ykca. Xaaaaaarliig Kaaagamaat Practlaa laiplamaalaili
R. Page 14 of 98
la amt appScakla. plaaaa arplatn. Practice. DSW 108001
WATER_PCB-SD0000021549
CAER Code of Management. Practices January 8. 1992 -- Page 5
Emergency Reiponie
1. An ongoing assessment of potential risks to employees and local communities resulting from accidents or other emergencies.
...... Comtnents on Category NA;.
Cateyorix NA EV DP IA PP RI
_i i
2. A current, written facility emergency response plan which address, among other things, communications and the recovery needs of the community after an emergency.
Comments on Category NA:.
3. An ongoing training program for those employees who have response or communications responsibilities in the event of an emergency.
Comments on Category NA:.
4. Emergency exercises, at least annually, to testoperability ofthe written emergency response plan..
Comments on Category NA:
5. Communication of relevant and useful emergency planning information to the Local Emergency Planning Committee.
Comments on Category NA:.
cu(r iu Ciuiercr
Category Of Catagary 1A Catagaty IV Calagary K
He Im
Pwlqill pla U >rmetlca U yhn.
ImiiiriiH Konagamaat HicUn tepb
it pictlM la *e appBcafclo. plaaaa aiplala OSW 108002
R. Page 15 of 98
WATER_PCB-SD0000021550
CAR Code of Management Practices January 6. 1992 -- Page 6
Citcgnriri
KA EV DP 1A PP RI
6. Facility tours for emergency responders to promote emergency preparedness and to provide currentknowledge offacility opera
tions.
.
Comments on Category NA:,
7. Coordination of the written facility emergency response plan with the comprehensive community emergency response plan and other facilities. If no plan exists, the facility should initiate community efforts to create a plan.
Comments on Category NA:
6. Participation in the community emergency response planning process to develop and periodically test the comprehensive community emergency response plan developed by the Local Emergency Planning Committee.
Comments on Category NA:
.
9. Sharing of information and experience related to emergency response planning, exercises, and the handling ofincidents with other facilities in the community.
Comments on Category NA:
Notes: Please identity any specific problems and/or resources.
Ctlifvy KA Catagary 1A Catagaqr IT Category U
Page 16 of 98
Ha aetlaa. Baa actlaa takaa Satan tfca aaaageaaaat practice la aat applicable. placet tiplala. *tlaadag txUtlaf taapaay practice# agafatat the Wn^wl Piactlaa. Dnatofiai pla ta teptemaat Maaagamaat Practice. lmpUmtla| actlaa plea Mm|int Practice la place Saaaaaaahis Maaagamaat Practice tmpleiaaatadaa.
OSW L08003
WATER_PCB-SD0000021551
ResponsibleGare: A Public Commitment
DISTRIBUTION CODE OF MANAGEMENT PRACTICES
Purpose
The purpose of the Distribution Code ofManagement Practices is to reduce the risk ofharm posed by the distribution ofchemicals to the general public; to carrier, distributor, contractor and chemical industry employees; and to the environment. Adherence to the code will lead to continually safer chemical distribution and help member companies to: evaluate the risks associated with ^hAmiral distribution and methods to reduce those
risks; meet or exceed all regulations and industry standards governing chemical distribution.; provide emergency advice and/or assistance to people on the scene in the event of a
chemical distribution emergency; develop new technologies and methods to improve chemical distribution safety. The code will also promote improvements in: 3 employee preparedness and awareness in preventing distribution emergencies; the safety performance of carriers and other providers of distribution services; 3 the public's preparedness in responding to chemical distribution emergencies;
OSW 108004
R. P*ge 17 of 98
WATER_PCB-SD0000021552
Distribution Code of Management Practices January 15, 1991 -- Page 2
the public's understanding of, and confidence in, industry efforts to improve chemical
distribution safety.
.
The Distribution Code of Management Practices applies to all modes of transportation
(highway, rail, marine, air and pipeline) and to the shipment of all chemicals, including
chemical waste. The code also applies to distribution activities (storage, handling, transfer
and repackaging) while chemicals are in transit between member companies and their
suppliers and customers. The implementation ofa number ofpractices ofthe code will vary
according to the characteristicsoftHechemicahbeingdistributed themode oftransportation
and the type of distribution activity involved.
' ~
Relationship to Responsible Care Guiding Principles
This code helps achieve several Responsible Care Guiding Principles:
to recognize and respond to community concerns about chemicals and our operations;
to make health, safety and environmental considerations a priority in our planning for all existing and new products and processes;
to counsel customers on the safe use, transportation, and disposal of chemicals;
to operate our plants and facilities in a manner that protects the environment and the health and safety of our employees and the. public;
to participate with government and others in creating responsible laws, regulations and standards to safeguard the community, workplace and environment; and
to promote the principles and practices ofResponsible Care by sharing experiences and offering assistance to others who produce, handle, use, transport or dispose ofchemicals.
Management Practices
Each member company shall have an ongoing chemical distribution safety program that
includes senior management commitment through policy* communications and resources to
improvements in chemical distribution safety. The program should include the following
elements:
'
1. Risk Management
1.1 Regular evaluations ofchemical distributionriskswhichconsider the hazards ofthe material, the likelihood of aeddentsfinddents and the potential for human and environmental exposure from release of the material over the route oftransport.
1.2 Implementation of chemical distribution risk reduction measures that are appro* priate to the risk level.
Page 18 of 98
os,, 108005
WATER_PCB-SD0000021553
Distribution Code of Management Practices January 15.1991~ Page 3
1.3 Internal reporting and investigation of chemical distribution acddents/xnddents. and implementation of preventive measures.
2. Compliance Review and Training
2.1 A process for monitoring changes and interpretations of new and existing regula tions and industry standards for their applicability to the company's chemical dis-
........ tribution activities, and for implementing those regulations and standards^_____
2.2 Training for all affected company employees in the proper implementation of applicable regulations and company requirements.
2.3 A program for providing guidance and information to carriers, distributors and contractors who perform distribution activities for the company on the company's training and compliance requirements for the activities.
2.4 Regular reviews of company employee, carrier, distributor and contractor compli ance with applicable regulations and company requirements.
3. Carrier Safety
3.1 A process for qualifying carriers of all modes and types (common, contract, private and customer controlled) that transport chemicals to and from company facilities that emphasizes carrier safety fitness and regulatory compliance, and includes regular reviews of their performance and compliance.
3.2 Feedback to carriers on their safetyperformance and suggestions forimprovement.
4. Handling and Storage
4.1 Documented procedures for the selection and use ofcontainers that are appropriate for the chemical being shipped, in compliance with testing and certification requirements, and free ofleaks and visible defects.
4.2 Documented procedures forloadingchemicals at company facilitiesthatwill reduce emissions to the environment, protect personnel and provide securement of the lading during transit.
4.3 Documented procedures for unloading chemicals at the company's facilities that will reduce emissions to the environment, protect personnel, and provide for safe unloading into proper storage facilities.
4.4 Defined criteria for the cleaning and return of tank cars, tank trucks, marine vessels, and retumable/refillable bulk and semi-bulk containers, and for the proper disposal of cleaning residues.
OSH 108006
R, P*ge 19 of 98
WATER_PCB-SD0000021554
Distribution Code of Management Practices January IS,1991 - Page 4
4.5 A program for providing guidance and information to customers, distributors, and other receivers on proper procedures for unloading and storing the company's chemicals.
4.6 A process for selecting distributors and other facilities that store or handle the company's chemicals in transit that emphasizes safety fitness and regulatory com pliance and includes regular reviews of their performance and compliance.
4.7 Feedback to distributors and operators of other facilities that store or handle chemicals in transit on their safetyperformance and suggestions for improvement.
5. Emergency Preparedness
5.1 A process for responding to chemical distribution accident/incidents involving the
company's chemicals;
.
5.2 Documented procedures for making information about the company's chemicalsin distribution available to response agencies.
5.3 A program for making facilities and/or training materials available to emergency response agencies.
5.4 Dialogue with state andlocal emergencyplanningorganizations on the distribution and hazards of the company's chemicals to improve community preparedness to respond to chemical distribution emergencies.
5.5 Dialogue with the public on their concerns about chemical distribution safety, actions taken bytheindustryand the companytoimprove the safetyofchemical dis tribution, and the effectiveness of emergency preparedness and emergency re
sponse assistance.
Member Self Evaluation
Member companies shall report annually the stage ofimplementation ofeach management practice in this code to an agent designated by the Chemical Manufacturers Association.
Relationship to Other Codes of Management Practice
This Code complements, and should be implemented in copjunction with, current and future Codes of Management Practices.
R. Page 20 of 98
lO 0OO.7
os#
WATER_PCB-SD0000021555
SAMPLE
A Public Commitment
CHEMICAL MANUFACTURERS ASSOCIATION MEMBER SELF-EVALUATION FORM
DISTRIBUTION CODE OF MANAGEMENT PRACTICES Member Company Name:_____________________ Responsible Care Coordinator Name:_____________________ Address:___________________
Telephone (__
losoos
R. Page 21 of 98
WATER_PCB-SD0000021556
R. Page 22 of 98
DSW 108009
WATER PCB-SD0000021557
MemDer Seu-tvaiuauon form
January 15, 1991 -- Page 2
Member Self-Evaluation Distribution Code of Management Practices
1. Under the Responsible Care initiative, each member company must submit a Self Evaluation Form annually to CMA or its designated representative. The annual self reporting has three purposes:
to establish an industry baseline from which to demonstrate continual progress in implementation of the Code.
to assist individual member companies in establishing a base line from which to set priorities for future development; and
to assist the industry (CMA) in designing programs to assist the member companies in achieving the goals of the Responsible Care initiative.
2. TO ESTABLISH THE INDUSTRY BASELINE, EACH MEMBER COMPANY SHOULD COMPLETE THIS SELF-EVALUATION FORM AND SEND IT BY C.O.B., MAY 23, 1991
3. The Distribution Code is unique in the sense that it deals with both products and facilities, but more importantly it deals with a broad range of third party providers of services and many external organizations and communities. This is considerably different than the CAER, WARE and Process Safety Codes, which deal primarily with fixed facilities and, as a result, have a more common base for self-evaluation. In contrast, different self-evaluation bases for each element of the Distribution Code will likely be more helpful and appropriate.
4. Self-evaluations for the Distribution Code should be expressed as percentages since the different bases for Code elements may not always be countable units. Therefore, the evaluation of each of the 21 separate elements ofthe Distribution Code ofManagement Practices should show what percentage of the company's distribution process is at each of the six implementation stages. For example, for a specific Code element, a company could report that 10% oftheir distribution process is at stage 1,50% at stage H, 30% at stage IH, 10% at stage IV and 0% at stages V and VI. Judgment will be required on how to develop these percentages, both in terms of what base to use for the calculation, and how to reflect centralized and/or decentralized distribution activities. Mostimportantly, each company will need to establish a methodology that will remain constant over the years in orderto measure annual progress. The suggestions under Item4 below are meant to assist you in developing your self-evaluation methodology.
5. The following bases for evaluation can be applied to a number of specific code elements:
Corporate programs, such as a corporate emergency response process, may be viewed as applying across the company for purposes of completing the Self Evaluation Form. The percentage implementation would result from judgment of
DSW 108010
R Page 23 of 98
WATER_PCB-SD0000021558
R. Pipe 24 of 98
OSW 108011
WATER PCB-SD0000021559
Member Self-Evaluation Form January 15, 1991 -- Page 3
sample
the existence and implementation of that process, or progress upon your own implementation action plan.
Alternatively, decentralized programs, such as site or division specific emergency response processes, should be judged as separate processes. A large multi-division company may have multiple emergency response processes to considerin establish ing a percentage of implementation.
Risk management activities are often undertaken on a product specific basis. Each company deals with a very large number ofproducts which are hazardous or nonhazardous, and must select a basis from which to evaluate and report future progress in implementing the Code. Judgmentis required to make sure that a large number ofnon-hazardous products which the company produces or distributes do not distort the evaluation. They should also not decrease the validity ofthe base for future evaluations.
Carrier safety reviews should be based on the number ofcarriers that fall under the code. Judgmentmustalsobe used where datais notreadily available on all carriers. The time spent on determining this basis will provide good information for progressing toward full implementation.
The number of third party providers of services to your company can serve as the basis for determining percentages of implementation in each stage.
Customer related elements should be evaluated on the basis of the number of customers, the hazardous nature ofthe products, and/orby the company divisional or business unit programs.
There are some elements, such as loading and unloading procedures, that are site specific and should be evaluated on that basis.
6. It is recognized that self-evaluation methodologies will vary from company to company. Because of this, flexibility has been built into the evaluation process. The basis for evaluating a company's distribution process should be established, documented and applied consistently for each annual self-evaluation exercise.
7. The six implementation stages are:
Stage I Stage II Stage m Stage IV Stage V Stage VI
No action Evaluating company practices against Code practices Developing action plan to implement Code practice Implementing action plan Code management practice in place Implementation reviewed and reaffirmed this year
OSH 108Q12
R. Page 25 of 98
WATER_PCB-SD0000021560
Member Self-Evaluation Form January 15, 1991 - Page 4
Risk Management PracticesIII HI IV
1.1 Regular evaluations of chemical dis
tribution risks which consider the haz
ards ofthe material, the likelihood of
accident5/inddents and the potential
far human and environmental exposure from release ofthe material
----
over the route of transport.
------- -
-
V____________________VI
--- ----- -- --
--
1.2 Implementation of chemical distri bution risk reduction measures that are appropriate to the risk level.
1.3 Internal reporting and investigation of chemical distribution acddents/inddents, and implementation of pre ventive measures.
J
v*
Compliance Review and Training
2.1 A process for monitoring changes and interpretations of new and existing regulations and industry standards for their applicability to the company's chemical distribution activities, and for implementing those regulations and standards.
2.2 Training forall affected company em ployees in the properimplementation ofapplicable regulations and company requirements.
2.3 A program for providing guidance and information to carriers, distributors and contractors who perform distribution activities for the company on the company's training and compliance requirements for the activities.
2.4 Regular reviews ofcompany employee, carrier, distributor and contractor com pliance with applicable regulations and company requirements.
R. Page 26 of 98
X)SM 108013
WATER PCB-SD0000021561
Member Self-Evaluation Form January 15, 1991 -- Page 5
Carrier Safety
I ________ III
3.1 A process for qualifying carriers ofall inodes and types (common, contract,
private and customer controlled) that transport chemicals to and from company facilities that emphasizes carrier safety fitness and regulatory ----compliance, and includes regular
reviews of their performance and compliance.
- - - -- ----------
3.2 Feedback to carriers on their safety performance and suggestions for im provement.
IV V
VI
--- -- A%
Handling and Storage
4.1 Documented procedures for the selec tion and use of containers that are appropriate for the chemical being shipped, in compliance with testing and certification requirements, and free of leaks and visible defects.
4.2 Documented procedures for loading chemicals at company facilities that will reduce emissions to the environ ment, protect personnel and provide securement ofthe lading duringtran sit.
4.3 DneuTngnted prneednrag fnr iinlAadiwg
chemicals at company facilities that will reduce emissions to the environ
ment, protect personnel, and provide
for safe unloading into proper storage
facilities.
.
4.4 Defined criteria for the cleaning and return of tank cars, tank trucks, marine vessels, and retumable/refillable bulk and semi-bulk containers, and for the proper disposal of clean ing residues.
\.5 A program for providing guidance and information to customers, distribu tors, and other receivers on proper
OSW 1080
R, Page- 27 of 98
WATER PCB-SD0000021562
Member Self-Evaluation Form January 15, 1991 - Page 6
Handling and Storage______
SAMPLE
I II_____ HI IV V
VI
procedures for unloading and stor ing the company's chemicals.
4.6 A process for selecting distributors and other facilities that store or handle
... the company's chemicals in transit that emphasizes safety fitness and -- -- --------------------_
regulatory compliance, and includes regular reviews oftheir performance and compliance.
-- --...... -.
4.7 Feedback to distributors and operators ofother facilities that store or handle chemicals in transit on their safety performance and suggestions for improvement.
Emergency Preparedness
5.1 A process for responding to chemical distribution accidents/intidents in volving the company's chemicals.
5.2 Documented procedures for making
information about the company's chemicals in distribution available to response agencies.
5.3 A program for making facilities and/ or training materials available to emergency response agencies.
5.4 Dialogue with state and local emer gency planning organizations on the distribution and hazards of the com pany's chemicals -to improve commu nity preparedness to respond to chemi cal distribution emergencies.
5.5 Dialogue with the public on their concerns about chemical distribution safety, actions taken by the industry
and the company to improve the safety ofchemical distribution, and the ef
fectiveness of emergency prepared ness and emergency response assis tance.
R. Page 28 of 96
OSW L080L5
WATER_PCB-SD0000021563
Distribution Code of Practices
Questions and Answers
1. What is the distinction between a distribution emergency and a distributiOTi accident/
incident?
.
Answer:
An accident/incidentis a definite and distinct occurrence ofan undesirable event. It may
involve an accident (traffic, derailment, collision, mishandling) ornearmiss, or be a result of a non-accidental container or operational failure. The undesirable effect can range from a small release of product (but major media coverage) to a major release with subsequent loss of property or personal injury.
An emergency is simply an accident/incident that requires immediate action.
In the context ofthe code, we distinguish between the two because we have direct control or influence over the causes ofaccidents and incidents. Many circumstances that dictate the emergency nature ofthe situation are most often outside ofour sphere ofcontrol and influence.
2. The words process, program, documented procedures and defined criteria are used throughout the code. What do they mean?
Answer: A program is meantto mean an organized list ofprocesses and procedures. In developing
a comprehensive distribution safety program the management practices ofResponsible Care should be included in the list ofprocesses and procedures. In a hierarchy ofterms, a program lies below a policy (a general statement of commitment or philosophy) and somewhere above a process or procedure. A program must address management needs, as expressed by policy, and contain feedback and measurement steps to determine if the needs are being met.
A process is a series ofrelated activities or actions that will lead to the desired end result. In the context ofthe code we have used process when itis dear the process can take many different forms, yet still provide the desired results.
Documented procedures are specific instructions or steps required to complete a task successfully. They may be written procedures or videotaped procedures, for example, that are to be explicitlyfollowed and are notleft open to interpretation. They are the most detailed step in the heirarchy, below policies, programs and processes.
Defined criteria are the ground rules around which a process or a procedure must be developed. In the code, the term is used to provide criteria to a third party that would enable that party to develop a process or procedure to lead to the desired end.
02m 1080X6
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WATER_PCB-SD0000021564
Questions and Answers January 15, 1991 - Page 2
3. Reference is made in the code to adherence to industry standards. What is meant by this0
Answer: The term industry standards, means those agreements, developed and complied with voluntarily, by a wide range ofco-producers, interindustrygroups and trade associations. Many of these agreements, in time, result in regulations or rulemaking procedures. It may also apply to a company's own internal standards of operation or practice.
4. The term, regular reviews, is used when referring to carrier safety performance, contractor and distributor performance and regulatory compliance. Whatis meantby the' term, regular review?
Answer: Regularreviews is a term used to measure ortest whetherour expectations are being met. They are crucial formanaging the whole distribution safetyprocess. By regular, we allow room for periodic or random reviews and allow the company to determine its own frequency ofreviewfor each element ofthe code, where itisappropriate. Reviews can take many forms, ranging from on-site and detailed audits, to presentations ofprogress with charts and graphs. This also allows incorporation of many of the safety performance reviews into quality and service review initiatives.
5. The code refers to cleaning and return ofreturoable/refillable containers. What is meant by returoable/refillable?
Answer: Returnable containers are those containers specifically designed for return to the company for reuse without reconditioning or reworking the container. Generally,, this typically only applies to containers of 55 gallons and above. The EPA is developing regulations regarding refillable containers that would drop below 55 gallons. Tank trucks, tank cars and marine vessels may or may not normally return to the company. Often, they are cleaned and placed back in general service.
All ofthe containers listed above are examples ofreturoable/refillable containers. For the purpose of the Distribution Code we must define criteria aimed at developing proper cleaning and residue disposal of these containers. Non-refillable, non-returnable containers are not covered under this code.
6. What is meant by regular evaluations of chemical distribution risks?
Answer:
How often distribution risk studies should be conducted will depend significantly on the chemical involved and the dynamics ofthe distribution. Evaluations should be regular in the sense they become a normal and routine part of distribution activities and are conducted often enough to respond to technology changes and operating experience.
Page 30 of 98
DSW 108016.01
WATER_PCB-SD0000021565
Questions and Answers January 15, 1991 - Page 3
7. The code requires dialogue with state and local planning organizations and the general public. What do we mean by dialogue?
Answer.
_,
#
Dialogue is simply two-way conversation. It implies that both parties listen and respond
to each other in a constructive way. With state and local planning organizations, the
dialogue will naturally focus on the more technical and factual aspects of chemical
distribution. Dialoguewith thepubhcwill involvemoreeducational types ofinterchange
for both parties. t
DSW 108017
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WATER_PCB-SD0000021566
R. Page 32 of 98
OSW 108016
WATER PCB-SD0000021567
April 6. 1990 AmcndH Scpirmbcr A. |99l
Responsible Care: A Public Commitment
POLLUTION PREVENTION
CODE OF MANAGEMENT PRACTICES
Purpose.
This Code is designed to achieve ongoing reductions in the amount or all contaminants and pollutants released to the airt water* and land from member company facilities. These reductions are intended to respond to public concerns with the existence of such releases, and to further increase the margin of safety for public health and the environment.
The Code is also designed to achieve ongoing reductions in the amount of wastes generated at facilities. These reductions are intended to help relieve the burden on industry and society of managing such wastes in future years.
In implementing the Code, each company should strive for annual reductions, recognizing that production rates, new operations, and other factors may result in increases. Despite these fluctuations, however, the goal is to establish a long-term, substantial downward trend in the amount of wastes generated and contaminants and pollutants released. Quantitative reduction goals will be established for giving priority to those pollutants, contaminants and wastes of highest health and environmental concern.
This code also includes practices that address the broader waste management issues beyond source reduction and other waste and release reduction efforts. Each member company must manage remaining wastes and releases in a manner that protects the environment ana the health and safety of employees and the public.
This Code complements, and should be implemented in conjunction with current and future Codes of Management Practices. Key terms arc defined in the Glossary, which should be consulted for assistance in interpreting the provisions of this Code.
0Sw 10801.9
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WATER_PCB-SD0000021568
Pollution Prevention Code . Peg# 2
Relationship to Guiding Principles
Implementation or this Code helps achieve the following Guiding
---- ------------ Principles;--
.... --------------------------------.......----------- ----
o To recognize and respond to community concerns about chemicals and our operations;
o To develop and produce chemicals that can be manufactured, transported, used and disposed of safely.
o To make health, safety, and environmental considerations a priority in our planning for all existing and new products and processes;
o To report promptly to officials, employees, customers and the public, information on chemical*related health or environmental hazards and to recommend protective measures.
o To operate our plants and facilities in a manner that protects the environment and the health and safety of our employees and the public;
o To extend knowledge by conducting or supporting research on the health, safety, and environmental effects of our products, processes, and waste materials.
o To promote the principles and practices of Responsible Care by sharing experiences and offering assistance to others who produce, handle, use, transport, or dispose of chemicals.
o To work with others to resolve problems created by past handling and disposal of hazardous substances.
o To participate with government and others in creating responsible laws, regulations and standards to safeguard the community, workplace and environment
o To promote the principles and practices of Responsible Care by sharing experiences and offering assistance to others who produce, handle, use, transport or dispose of chemicals.
R. Page 34 of 98
OSU 108020
WATER PCB-SD0000021569
Pollution Prevention Code Page 3
Management Practices.
Each member company shall haw a pollution prevention program which shall include:
1. A clear commitment by senior management through policy, communications, and resource, to ongoing reductions at------
each of the company's facilities, in releases to the air, water, and land and in the generation of wastes.
2. A quantitative inventory at each facility of wastes generated and releases to the air, water, and land, measured or estimated at the point of generation or release.
3. Evaluation, sufficient to assist in establishing reduction
priorities, of the potential impact of releases on the
environment and the health and safety of employees and the
public.
'
4. Education of, and dialogue with, employees and members of the public about the inventory, impact evaluation, and risks to the community.
5. Establishment of priorities, goals and plans for waste and
release reduction, taking into account both community concerns and the potential health, safety, and environmental impacts as determined under Practices 3 and 4.
6. Ongoing reduction of wastes and releases, giving preference first to source reduction, second to rccydc/rcusc. and third to treatment. These techniques may be used separately or in combination with one another.
7. Measurement of progress at each facility in reducing the generation of wastes and in reducing releases to the air, water, and land, by updating the quantitative inventory at
least annually.
8. Ongoing dialogue with employees and members of the public regarding waste and release information, progress in achieving reductions, and future plans. This dialogue
* should be at a personal, face-to*face level, where
possible, and should emphasize listening to others and discussing their concerns and ideas.
9. Inclusion of waste and release prevention objectives in research and in design of new or modified facilities, processes, and products.
nsw 108021
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WATER_PCB-SD0000021570
Pollution Prevention Code Pago 4
10. An ongoing program for promotion and support of waste and
release reduction by others, which may, for example,
include:
*
a.----- Sharing of technical information and experience with --------------- customers and suppliers;
b. Support of efforts to develop improved waste and release reduction techniques;
c. Assisting in establishment of regional air monitoring networks;
d. Participation in efforts to develop consensus approaches to the evaluation of environmental, health,
and safety impacts of releases;
c. Providing educational workshops and training materials;
f. Assisting local governments and others in establishment of waste reduction programs benefUting the general public.
11. Periodic evaluation of waste management practices associated with operations and equipment at each member company facility, taking into account community concerns and health, safety, and environmental impacts and implementation of ongoing improvements.
12. Implementation of a process for selecting, retaining, and reviewing contractors and toll manufacturers taking into account sound waste management practices that protect the environment and the health and safety of employees and the
public.
13. Implementation, of engineering and operating controls at each member company facility to improve prevention of and early detection of releases that may contaminate
groundwater.
14. Implementation of an ongoing program for addressing past operating and waste management practices and for working with others to resolve identified problems at each active
or inactive facility owned by a member company taking into account community concerns and health, safety, and environmental impacts.
R. Page 38 of 98
OSM 108022
WATER_PCB-SD0000021571
Pollution Prevention Code . Page 5
Industry Trend Data To develop and maintain statistical industry trends. CMA will collect currently available data. Each company shall report annually to CMA. or its designated agent, for each facility:
o Releases of substances as reported under SARA Section 313; and
o Wastes generated, as defined and reported in CMA's annual waste survey.
Member Self-Evaluation. Each member company shall report annually to CMA, or Us designated agent, the stage of implementation of each management practice in this Code. The reports shall be on the member self-evaluation form attached as Attachment A.
OSW U18023
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WATER_PCB-SD0000021572
Pollution Prevention Code Page 6
Glossary* of Terms
As used in this Code, key terms arc defined as set forth below. Note that these definitions may be broader than regulatory definitions, and that adherence to this Code does not relieve a company of the obligation to meet Federal, state and local regulatory requirements.
Facility - A site used for chemical manufacturing, processing, refining, packaging, R&D, distribution or related commercial activity.
Recycle A practice which regenerates or processes a material from a process to recover a useable product or material for reuse.
Release - Any emission, effluent. spill, discharge or disposal to the air. land, or water, of any pollutant or contaminant whether routine or
accidental, at or from a facility. The term does not include shipment or
distribution of chemical product nor release to the environment as part of normal and intended use of a product by the consumer.
Reuse - A practice that rccmplovs a material from a process cither as an ingredient in a process to make a product or as an effective substitute for a commercial product in a particular function or application.
Source Reduction * A practice that reduces the amount of any release or waste generated at the source, including closed loop recycle and reuse before exit from a process. The term includes, among other practices, equipment and technology modifications, process and procedures modifications, reformulation and redesign of products, substitution of raw materials, and improvements in housekeeping, maintenance, training and inventory control.
Treatment - A practice, other than recycle or reuse, that alters the physical, chemical, or biological characteristics or the volume of a waste through a process or activity separate from the production of a commercial product or the provision of a service.
Waste - Any gas, liquid, or solid residual material at a facility,
whether hazardous or non hazardous, that is not used further in the production of a commercial product or provision of a service and which itself is not a commercial product.
R. Page 38 of 98
osw 10802* WATER PCB-SD0000021573
POLLUTION PREVENTION CODE
REPORT 1: MEMBER SELF-EVALUATION FORM FOR THE 1991 REPORTING YEAR
Instructions for the Company Responsible Care* Coordinator.
1. This form is to be submitted annually to CMA by each member company. This year the due date Is XXX SI. 1992. Please submit directly to:
2. Indicate on page 1 the number of your member company's facilities that are subject to the Code. Rarh company's Responsible Care* Coordinatormust report the implementation stage for all facilities subject to the PoDutlon Prevention Code on this farm.
3. The Self Evaluation form for the 1991 reporting year covers fourteen management practices. DO NOT COMPLETE THIS FORM. (CMAwlH send the SelfEvaluation Form farthe 1991 reporttngyeartnApril/May 1992.)
4. Far Management Practices 1-11 and 13 on the following pages, indicate the number of facilities that have attained each implementation category. Identify the current implementation category for each of your facilities at the nww you complete the farm. Formanagementpiactlces 12 & 14. indicate the company-wide reporting using a percentage (following instructions on page 5).
5. For the Industry Trend Data, show the total number offacilities tn each appropriate box. The total number of faculties for each type of Trend Data should equal the total number of faculties subject to the Code.
6. Only subject facilities owned or operated as of the reporting date should be included.
7. The implementation categories are:
Category NA - No action. Ifno actiontakenbecauaethemanagementpractice Isnot applicable, please explain. Category EV - Evaluating existing company practices against the Management Practice. Category DP - Developing plan to implement Management Practice. Category IA - Implementing action plan Category PP - Management Practice m place. Category R1 - Reassessing Management Practice implementation.
8. Ifany facilities are shown in Category NA. please add anypertinent rosaries to the space marked "comments."
*oa0*s
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WATER_PCB-SD0000021574
POLLUTION PREVENTION CODE OF MANAGEMENT PRACTICES
REPORT 1: MEMBER SELF-EVALUATION FORM FOR THE 1991 REPORTING TEAR
l
Member Company Name:_____ ________________ Responsible Cere* Coordinator Name:__ Address;
Telephone: ( 1 Number of facilities subject to the Pollution Prevention Code
R. Page 40 of 98
OSW 108026
WATER_PCB-SD0000021575
POLLUTION PREVENTION CODE
Industry Trend Data
V
Report annually to CMA or its designated agent, the number of facilities far which annual report to CMA has
has not been submitted:
'
Member Company Name:.
Annual Baport Submitted*
T-l. Release of substances as re ported underSARASection313: and
T-2 Wastes generated, as defined and reported in CMA's annual waste survey.
Form R
j Form 1 _HR_ 1 1
Annual Raport Mat ubmlttad*
Total FaeUmaa
'Enter the number of facilities.
NOTES:
1. CMA expects to receive release data only from those facilities that are required to complete the Form R following the requirements in the Superfund Amendment and Reauthorlzatlon Act (SARA! Section 313 and EPA's clarifying regulations and instructions.
2. Instruction: Under Form R. enter the number of facilities that are submitting TR1 data to CMA.
line T-l:
Q These facilities should submit the same data as ERA requires. The 313 Form R release data are due to ERA on Jufy 1.1992 and to CMA an July 31.1992.
Under Form NR. enter the number of facilities that are not subject to the EPA reporting requirements. These facilities should complete Form NR Companies, not required to report 313 release data to EPA. mav volunteer to mend release data to CMA. These facilities are not required to submit TRI release data to CMA as an obligation of membership.
line T-2:
The 1991 Reportingyear is the first year thatfacilities must complete CMA's annual Waste Survey as an obligation of membership under the Pollution Prevention Code.
IJOBOZJ
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WATER_PCB-SD0000021576
POLLUTION PREVENTION CODE OF
Management Practice*
MANAGEMENT PRACTICES
Categories
IU XV OP 1A
^\
PI*1 RE
1. A clear commitment by senior management through policy, communications, and resources, to ongoing reductions, at each of the company'* facilities, m releases to the air. water, and land and in the generation of wastes.
2. A quantitative inventory at each ifccfflty ofwastes generated and releases to the air. water and land, measured or estimated at the point of generation or release.
torments on Catenary NA:
3. Evaluation, sufficient to assist in establishing reduction priorities, of the potential impact of releases on the environmeni and the health and safety ofemployees and the public.
torments on Category NA:
4. Education of. and dialogue with, employees and members of the public about the inventory, impact evaluation, risks to the community.
torments on Category NA:
..........
f
CiUfay XA Ct|iy CT CHimyDP Cili(7U
c*tg7 rr
CltlfMJ B2
R. Page 42 of 98
R*k8m. geo actfoa lafaa >inm Q--ysstl-- toat ifyBtaMa.
8*hitla< 8i iU| itapuy yneltM agalaat tfca Mnnwal PiaaUaa.
D**tapa| flaa to tapWmMt PTifmet pioatlaa. laptiaadai octloe plae Kuqraal fnctln te pkao.
Kuu|n<at Practice taplamoetatloe.
OSM 108028
WATER_PCB-SD0000021577
r4.
Catcaorlea NA EV OP
5. Establishment of priorities, goals and plans for waste and release reduction, taking into account both community concerns and the potential health, safety, and environmental trnpan* as determined under Practices 3 and 4.
Comments on Category NA:,
Rl
6. Ongoing reduction ofwastes and releases, giving preference first to source reduction, second to recycle/reuse, and third to treatment These techniques may be used sepaxatety or m combination with one another.
Comments on Category NA:
_________
7. Measurement of progress at each facility tn reducing the generation of wastes and in reducing releases to the atr. water, and land, by updating the quantitative inventory at least annually.
Comments on Category NA:
8. Ongoing dialogue with employees and mmbers cf the pubUc regarding waste and release intonation, progress to achieving reductionsand future plans. ThisdialogueshouldbestaperscnaL face-to-face level where possible, and should emphastee hstcntng to others and discussing their concerns and fcleM.
Comments on Category NA:.
C4U|7 IU Cttt|07 EV Ctti|r7 OP Ct|T U Ctiafi7 PP
Category U
IhtcdM. BMlwt>ii>iwiiOWM|w>t|nttfwfcMti||8Mlli,ytoMiaa.
trilutlai
caafuyynctlcM iidttt tko l*mnwi Piaadao.
Derotoptag pUa It Iwflwwt VihibwI Pixdoo,
tmpUmoadag aedaa plaa
K|taia( PnctiM la plus.
Itmwilni SUaafwmit Procdce layliawtitlM
SH 1 OSD 2 9
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WATER_PCB-SD0000021578
Categories
NA EV DP 1A PP
9. Inclusion of waste and release prevention objectives in research, and in design of new or modified facilities, pro* cesses, and products.
Comments on Category NA:.;
Ri
10. An ongoing program far promotion and support ofwaste and release reduction by others, which may, far example. Include:
a. Sharing of technical information and experience with customers and suppliers: *
b. Support ofefforts to develop Improvedwaste and release reduction techniques:
c. Assisting in establishment of regional air monitoring networks.
d. Participationm efforts to develop consensusapproaches to the evaluation for environmental, health, and safety impacts of releases:
e. Providing educational workshops and trainingmaterials:
Assisting local governments and othas m establishment of waste reduction programs benefiting the gmeral pubbe.
Comments on Category NA:
11. Periodic evaluation of waste management practices associ ated with operations and equipment at each member com pany facility, taking into account community concerns and health, safety, and environmental impacts and implementa tion of ongoing improvements.
Comments on Category NA:
Gatagerr KA Calegry XV CMi|7 DP CatagarylA
uit|U7 rr
Category B1
Page 44 of 98
Ha aattaa. Si* actfaa
hawi tka -----g---- pnetlea ia aat appScabla. plaaaa aiplata
t*lHtfi| aaUttag aaaapa*j practlaaa agataat tka Mm|aiit htelUt.
Oarataplaa plaa U tapli--t Mnafl Praattaa.
baplamaatlag trtta plaa
HiHfiMt htctlct la plaaa.
UmimmIm HuunMat Vractfaa tailiawiarta
,, _.
OS U 108030
WATER_PCB-SD0000021579
12. Sec Instructions below.
--N--A---- EV
Categoric* DP 1A
PP
RI
13. Implementation of engineering and operating controls at each
member company facility to Improve prevention and eazfy ---- ion Tarases that may PnntWTTM^. gpmmrfafter.
..... -
%
Infractions far Practices 12. ContractorJterlcw.
CMA recognizes that companies may Implement Practices 12 and 14 on a company-wide or even corporation-wide basis rather than on a facility baste. Therefore. CMAasks companies to complete the Self-EvaluationForm using percentages that represent company-wide implementation ibr these two practices. In adding up the total percentages aaoas all ofthe six categories, the numbermust equal 10046. Also, please use onlywhole numbers. Farthese two management practice* the numWothrimv. used to calculate the percentage may exceed the number offadhtles shown on page 1.
Companies may use ary appropriate method to calailate these percentages. One csudca companies will want to carefully consider
ralwilaMrtn t+ p-rfnrjnmA and nae an a yearly haste so that the data ha year to year can be compared mgartnftiPy
QttSgorlef
NA EV DP IA PP
12. lmplanentation ofa process Jarselecting, retiming. and reviewing contractors and ton manufacturers taking into account sound waste managenentpractices thatprotect the environment andthe health and safety of employees and the public.
Comments on Category NA:
RI
14. Implementation ofanongoingprogram firaddressingpastoperat ing and waste management practices and far working wflh others to resolve kjenuQed prebloos at each active or inactive facility owned by a member company, taking no account community concerns and health, safety. and envimnmmtal impacts.
Comments on Category NA:
C4U|7 ru C*l|t7 XT ctf7 or Ctti(7 U Catagsry IP Ci fry at
Us aetlam. ff actiaa taka twiwi tk saa|rsat yrmctlaa la sat tyybcahU. ylaaaa oyUS.
Erihadai trUtlng eaapaay praeticM sgataut tk* Maaagaaaat PnetUa.
Dmlrflag plu U laplisal Masagawaat PmBw.
Implementing actiai piaa
Mangmeat Pncttcr ta plaea.
IrainwlBf Managaaaaal Pnttlc fagplamaataUaa.
OSM 1-08032
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WATER_PCB-SD0000021580
Pollution Prevention Cod* Page 7
ATTACHMENT C
WASTE AND RELEASE REDUCTION CODE OF MANAGEMENT PRACTICES
QUESTIONS ANO ANSWERS
1. Is this s voluntary or mandatory policy?
Answer: Ths Vasts sad Release Reduction Cods of Management Practices has bsaa developed under CHA's Responsible Cars prograa. Adherence to ths Ssspoasibls Cara guiding principles is aa obligation of naabarship ia CMA.
2. Hast ths Management Praeticss bs coaplstad ia ths apscifie ordsr listsd?
Aaswar: Ths Maaagsasat Praeticss ars laid oat ia a logically sequential pattern to coaplsts a redaction project. Ths sequence should bs generally adhered to although slight re-arrangeseat under specific dreuastaaees aay bs warranted.
3. Since ths seqps of this policy covers all haaardoos and non-hazardous wastes and releases, doesn't the Code require too aueh too fast or dilute the focus froa hazardous pollutants?
Answer: The public is not seeing or ashing a distinction between hazardous and non-hazardous releases and wastes. Public opinion research shows that the public wants releases lowered and perforeanee inproved. This research indicates that the public is concerned about both ehealeals and trash generated by industry.
The definition of "hazardous" is not unifora throughout the United States, since nany states have their own definitions that are wore restrictive than the federal SPA's. Furthermore, these definitions of "hazardous" keep changing over tine.
Each'company is starting froa differing points. Each eoepany sust identify its own reduction opportunities, identify the concerns of its own public, determine the reduction priorities and goals, and develop and implement its own reduction plan. The goal of this Code is continued performance lmprovesent by a long term comaltaent to the reduction of wastes and releases.
R. Page 46 of 96
osw loao^2
WATER_PCB-SD0000021581
Pollution Prevention Code Pege 8
4. Why doe* this Cod* *pp*r to endorse redaction* for reduction* **k*7 Why should wastes and relsass* be reduced below health-based standards? Why should wastes and releases be reduced below levels allowed by statute, regulation, or permit?
Answer: The public does not endorse the concept of "permitted" feneration of wastes or releases to the eavlronnent. The public desires An Increased nargln of safety and envlronaental protection as a goal. Zf the policy Is to address the concerns of the public, It snist require sustained reductions.
5. Zs this Code a never-ending spiral of reduction?
Answer: The policy is flexible so that each coepany can assess the viability of further reductions. Certainly, reductions will be sustained under the Code as long as they are technically and econoaically viable. To the extent reduction options reaain viable, the goal is to establish a long-ten, substantial downward tread in wastes generated and releases to the eavlronnent.
6. Will this Cede cause eesber to aceoopllsh substantive reduction?
Answer: To achieve the goal of earning the public's trust through improved perfonaace, real reductions nust occur. Therefore, this Code has neasurable iapleneatatloa stages and Industry treads data subaissioa requireaeats.
7. Does this Code apply to both large and snail coapeales and facilities? Is there a threshold below which this Code does not apply?
Answer: The Code applies to all neabers of CHA. Evan a snail conpaay or facility can generate wastes and releases to the eavlronnent. There is no threshold for voluae of wastes geaersted, releases to theeavlronnent, or sise of facility below which this Code does not apply. Each coepany/facility will establish its own priorities. The Code envisions progress by all of Industry la reducing wastes and releases.
8. Does this Code apply to dooestlc or world-wide operations?
Answer: The principles behind the Code are universal in concept. The reduction of wastes and releases is good business and good citizenship. However, for purposes of CHA eligibility requireaeats, the Code applies to that portion of a corporation or conpaay that is used to deterniae CHA dues.
OSW 108033
R. Page 47 oi 98
WATER_PCB-SD0000021582
Pollution Prevention Code Page 9
9. Vhst-about ultl-divisionml companies? Does this Code apply to ainlug operations? Service atatlona? Harahouses?
An*war*: Adharaaea to the Coda of Managaaant Praetlea* Is a Guiding Principle of tha Xasponslbla Cara prograa. Tba Responsible Cara prograa la a aaabarablp requirement for tboaa portions of a coopany that dataraina tba CHA duas structure. The . principle of reducing wastes sad releases la responsible corporate behavior and should be encouraged throughout an organisation. ~
Tbs Vasts and Release leductloa Code of Hanageaent Praetlea Is dasignad for flaxlbls laplaaeatatioa by eoapanlas and faeilltlas. Each coopany/facility oust dataraina tba reduction opportunities, priorities* baseline* and lapleaaat the reduction plan In accordance with these coapany/facility-derived goals. Inherent In this Coda is tba need to cooaualcate with tba public when determining reduction opportunities and prioritise. Therefore, while the scope of this policy Is broad* each coopany oust Identify tba sources that are included la Its lapleaantatlon activities as well as the priority and timing for these reduction activities.
10. If all of the ehealeal industry is to be affected* how do we ensure fair and equitable reductions? How do we prevent eoapetltlve disadvantages aaong CHA samber coapanies?
Answer: The Vaste and Xelease leductloa Cede is predicated on aaklng reductions that are eceuoaleallj and technically sound. Tha Coda does not envision enforcing eoapetltlve disadvantages on amber coapanies by usurping their decision-asking processes. Each coapany east evaluate its own reduction opportunities and develop Its own reduction plan to aeet coapany/facility priorities.
11. Xf all of the ehealeal industry Is to be affeetad, how do wa ensure fair and equitable reductions? low do we prevent eoapetltlve disadvantages with other industry segaents?
Answer: This Cede will actually nuke our industry wore eoapetltlve than those that do not eabrace its concepts. Haste and release reductions will result in less wastes* laproved efficiency, and aaka tha industry a superior coepetitor.
12. Is this a non-growth Code? How can this Coda be reconciled with the need for expansions? How are opportunities for eaisslen offsets (needed for air permitting) to be preserved?
Answer: This Code envisions a long-tern* substantial downward trend la total releases to the environment and waste generation. However* the aethod of achieving reductions is left to tha needs and priority daterainations of tha individual aasbar coapanies.
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OSW 108034
WATER_PCB-SD0000021583
Pollution Prevention Code Pag* 10
The policy la not * no-grovth policy; rather, it la a policy of balancing fatore expansions with futara vasts and release reductions.
Voluntary vasts and release reductions nay be eligible to be banked vith appropriate governaental agencies. Any plan for vesta and release reductions Bust also plan to aeeossodate expansions. Public perceptions aay ultinately require a vasts and release reduction type pragma Just as a condition to be able to construct or expand. Several states already have proposed such regulations.
13. Won't this Code have enoraous econoale consequences?
Ansver: Waste and release reductions aay or aay not have a huge price tag. Soae reduction projects, like fugitive ealaslon abateaent, tend to pay for theaselves in recovered product(s); other projects aay increase the price of doing business. Industry sust be villing to invest in plants that will lead to a future with less vastes and fever releases to the environaent. The goal of Responsible Care is that the ebeaical industry vill iaprove the perforaance of Its operations constantly.
Zn aaking reduction progress, each eoapany aust look at all the reduction opportunities and set their ova priorities. Each eoapany can set the scope of these priorities broadly or narrowly and lapleaent actions at their ovn paee.
Each eoapany aust identify its ovn reduction priorities and iapleaent a reduction plan to aeet eoapany/facility-sat goals.
14. Does the hierarchy of reduction aethodologies seen that all projects aust use source reduction unless it is technically infeasible?
Answer: Eaeh waste and release source aust be evaluated for its reduction potential. The hierarchy requires that reduction projects fog source reduction be evaluated before reeycle/reuse or treatseat. However, the project to be lapleaeated vill depend on the evaluation.
Technical lnfeasibillty is only one of several facility and/or waste specific criteria that can lead to selection of a reduction project involving recycle/reuse or treatseat. When developing their reduction priorities, coapenles aay choose to consider other criteria including risk/benefit neehanlsas, public concern, sirs of the facility, ecoaoalcs, and other factors such as conservation of resources*
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15. Tbit Code, as veil as other eodes voder the Responsible Care prograa, require ongoing dialogues vlth eaployees and aeakers of the public. Does each such Hanageent Practices require a separate aeetlagT
.. Answer: No. Heatings vlth eaployees or the public can have avltlple agenda lteas. If several Hanageaant Practices lteas are to be covered in a single seating, all that is required la that the agenda end presentation dearly address eaeh topic, rather than have a general "discussion of topics."
Under the Responsible Care Prograa, the process to coaaunicate vlth the publle and eaployees Is established under the Coaaunlty Awareness and Eaergeaey Response (CAER) Code of Hanageaent Practice. Coapenies are encouraged to use the aeehanlsas set up under other codes to enhance effective lapleaentatlon of the Responsible Care Prograa and to better use and conserve coapany resources.
16. Is dialogue with the publle required for all facilities?
Answer: Meaningful dialogue is essential to better understanding public concern, laproving the public's understanding of our operations, and building trust. Sons facilities, due to slse and location, nay have Halted opportunity for such dialogue. Where the opportunity for dialogue exists, even on e Halted basis, it should be actively pursued individually or* Jointly with other neighboring coapenies/facilities.
17. Should individual coapanles and/or facilities subalt to CHA the rationale behind the annuel Industry Tread data subaisslons?
Answer: No. Tbs data subaltted for the Industry Tread Data reports need not have supporting docuaeatatlan subaltted to CHA. However, when discussing these data with the local public, it is assuaed that general aethods sad essuaptions will be discussed as part of the public education and dialogue process.
18. When eoepletlng the Self-Evaluation Fora, Bust every facility atteapt to progress through all the lapleaentatlon stages, or can soae facilities "nature" their progress la code lapleaentatlon at less than full lapleaeatatlonf
Answer: All participating facilities should work to achieve full lapleaentatlon of eaeh Code and eabraee the concepts of this Code In the spirit of the Responsible Care Guiding Principles. Depending on the sine of particular facility or the ectivltiea carried on by that facility, a coapany nay decide that different lapleaentatlon aethods are appropriate. For exaaple, a large facility aay use foraal procedures such as written policies and
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manuals mod conduct formal employee tint*. Vbereas, gBiier mfaecthiolditsy. can accomplish the same iepleeentation us in* leas foraal
SH 108037
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Attaehnent B
QUESTION AND ANSWERS FOR PRACTICES H-1*
Th*a* quMtioas address Issues In tb* four praetlcas added to tba Pollution Prevention Code of Manageaent Practices. As coapanles lapleeent Practices 1*10, they should axaalne their lapleaentatlon actions and codify thea to Include waste cans*event.
QUESTIONS:
IN PRACTICE II, WHAT ARE THE WASTE MANAGEMENT PRACTICES ASSOCIATED WITH AIL OPERATIONS ANO EQUIPMENT?
The Code envisions companies reviewing all waste aanageaent practices at each step of the operatlon(s) where wastes are generated or released within eaeh facility. This review is within the operstlng processes not just at the "end of the pipe."
WHAT 00 YOU MEAN BY A CONTRACTOR AND TOLL MANUFACTURER?
Contractors are any entity a neaber coopany uses to handle its secondary aatarlals and wastes. This Includes, for ezaaple, waste treatnent facilities, disposal facilities, tank cleaners, redaiaers, recyclers, and the like. "Contractors" does not Include publicly owned treataent works.
Responsible Cared covers toll aanufacturers* operations under two Codes. Ibis code covers the wastes generated by relevant operations of toll aanufacturers. For the purpose of this code, toll nanufaeturers are independent parties who: perfora a aanufacturlng step for a neaber coapany In which the neaber coapany owns the work In process; use the neaber coapany's feed stock; and generate waste froa the aanufacturlng step.
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ro i lUtoigii r i c ***< vm wuut
Page 14
WHAT DOES "IMPLEMENTATION OF A PROCESS. . .. MEAN?
The requirement for tb "Implementation of a process. . .i* designed to encourage aabr coapanles to do business with those contractor* and toll aanafactnrar* that, aftar raaaoaabla inquiry, arc believed to engage In sound vast* management praetlcaa.
As part of tha contracting procadnra, aaabar coapanlas should consider inclodinf languafa raqulrlnf tha contractor to us* proper health, safety, and anvlronaentel practices and statinf that the aeaber coapany has a rifht to inspect for that purpose.
HOW DO YOU REVIEW THAT A CONTRACTOR OR TOLL MANUFACTURER USES SOUNO WASTE MANAGEMENT PRACTICES?
A process for "reviewing" includes reasonahle review* of the relevant practices of contractors and toll aanufacturers. Because of the variety of.coaaerclal relationships and circuastancea, aeaber coapanles are to exercise their own judfeaent as to how to conduct "reviews" and precisely what to do with the inforeation obtained.
CHA aeaber* are not expeeted to control the operations of their contractors and toll aanufacturers. CHA aeaber eoapenies should consider performing a site visit and visual inspection of waste management practices by a coapany representative. The aeaber coapany aay determine that a wore rigorous inspection is appropriate based on initial findings.
HOW OFTEN SHOULD YOU REVIEW CONTRACTORS AND TOLL MANUFACTURERS?
A review or evaluation should be done on some repeat basis. Coapanles should deteralne the tlalng by an evaluation of the results of previous reviews, potential iapacts, potential liability, etc.
WHAT DO WE KEAN BY "IMPROVE THE PREVENTION OF RELEASES TO GROUNDWATER?"
The goal is *a prevent releases to the ground and to protect existing groundwater quality. While it is envisioned that a coapany will have an 5FCC (Spill Prevention Control and Counteraeasures) plan for certain materials, coapanles should review the ehealeals at the facility and extend the SPCC concepts to other aaterlals. To laprove efforts to prevent releases, aeaber coapanles should review the cbeaieals and operatlane et a facility; develop plane to prevent, detect, and contain releases or potential releases; and lapleaent these plans to protect groundwater froa contamination.
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IN PRACTICE 14 WHAT IS MEANT BY IMPLEMENTATION OF AN ONGOING PROGRAM TO RESOLVE IDENTIFIED PROBLEMS?
"implementation of an ongoing program..." noans developing processes for evaluating the health* safety, and envlronaental lupacts of identified problems ariaing from port operating and waste nanageeest practices and for setting priorities for addressing those probleas. The Coda recognises that sot every identified problea poses adverse impacts. Resolving identified probleas should consider factors such as, regulatory, technical, and eeonoaie considerations.
WHAT IS MEANT BY "PAST OPERATING AND WASTE MANAGEMENT PRACTICES?"
Past operating practices and waste aanagesant practices that companies should consider nay include operating practices such as: manufacturing operations, loading and unloading areas, storage, areas of spill containment, and recycling and reuse processes; and waste management practices such as: surface impoundments, waste treatment, land disposal, land treatment and faming, and deepwell injection.
WHAT IS MEANT BY "WORKING WITH OTHERS TO RESOLVE IDENTIFIED PROBLEMS?"
Each member company's program should Include a process to cooperate, to the extent appropriate, with governmental agencies, past owners, operators, insurance carriers, the community, and ethers to resolve the potential health, safety, and environmental impacts, and community concerns associated with identified problems.
WHICH MEMBER COMPANY FACILITIES, ACTIVE OR INACTIVE, ARE INCLUDED IN PRACTICE 14?
This practice applies to facilities currently owned by a member company. Thin includes properties that are still owned, but no longer have ongoing operations. Inactive sites that are not owned by a member company, hut where the company has potential involvement, should be addressed to the extent the member company determines feasible.
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WHAT IS MEANT BY "TAKING INTO ACCOUNT COMMUNITY CONCERNS AND HEALTH, SAFETY, AND ENVIRONMENTAL IMPACTS?"
When CKA aeaber companies lapleaaat the employee cad public outreach of the Code (Practices 4 and 8), companies should present information about their current and past vasts nanageseat practices vith the goal of identifying the coaaunity concerns. Coapanies should consider this input when developing plans and setting priorities for waste aanageaent and reaediatlon activities.
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Responsible Care: A Public Commitment
PROCESS SAFETY CODE pF MANAGEMENT PRACTICES
The Process Safety Code is designed to prevent fires, explosions and accidental chemical releases. The Code is comprised of a series of management practices that reflect this goal, with the expectation of continuous performance improvement for each management practice. The practices are based on the principle that facilities will be safe if they are designed according to sound engineering practices, built, operated and maintained properly and periodically reviewed for conformance.
Process safety is an interdisciplinary effort. Consequently, the Code is divided into the followingfour elements: management leadership, technology, facilities and personnel. Each element is composed of Management Practices. Individually, each Practice describes an activity or approach important to preventing fires, explosions and accidental chemical releases. Collectively, the Practices encompass process safety from the design stage through operation, maintenance and training. The scope of this Code includes manufacturing, processing, handling and on-site storage of chemicals. This Code must be implemented with full recognition of the community's interest, expectations and participation in achieving safe operations.
The process safety management program in each fadHty is complemented by workplace health and safety programs, as well as waste and release reduction programs which address and minimize releases and waste generation. These three programs, and others, will help assure that CMA member facilities are operated in a manner that protects the environment and the health and safety of personnel and the public.
Relationship to Guiding Principles
The Code helps achieve several of the Responsible Care Guiding Principles:
To recognize and respond to community concerns about chemicals and our operations,
To make health, safety and environmental considerations a priority in our planning for all existing and new plants and processes.
To operate our plants and processes in a manner that protects the environment and the health and safety of our employees and the public.
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Management Practices Each member company shall have an ongoing process safety program that includes:
Management Leadership .
1. Leadership by senior management through policy, participation, communications and resource commitmenu in achieving continuous improvement of performance.
.t
2. Clear accountability for performance against specific goals for continuous improvement.
3. Measurement of performance, audits for compliance and implementation of corrective actions.
4. Investigation, reporting, appropriate corrective action and follow-up ofeach incident that results or could have resulted in a fire, explosion or accidental chemical release.
5. Sharing ofrelevant safety knowledge and lessons learned from such incidents with industry, government and the community.
6. Use of the Community Awareness and Emergency Response (CAER) process to assure public comments and concerns are considered in design and implementation of the facility's process safety systems.
Technology 7. Current, complete documentation ofprocess design and operating parameters and procedures.
8. Current, complete documentation of information relating to the hazards of materials and process technology.
9. Periodic assessment and documentation of process hazards, and implementation of actions to minimize risks associated with chemical operations, including the possibility ofhuman error.
10. Managementofchanges to chemical operations to maintain or enhance the safety originally designed into the facility.
Facilities
11. Consideration andmitigation ofthe potential safety effects ofexpansions, modifications and new sites on the community, environment, and employees.
12. Facility design, construction and maintenance using sound engineering practices consistent with recognized codes and standards.
13. Safety reviews on all new and modified facilities during design and prior to start-up.
14. Documented maintenance and inspection programs that ensure facility integrity.
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.
15. Sufficient layers of protection through technology, facilities and employees to prevent escalation from a single failure to a catastrophic event.
16. Provision for control ofprocesses and equipment during emergencies resultingfrom natural events, utility disruptions and other external conditions.
Personnel
17. Identification of the skills and knowledge necessary to perform each job.
18. Establishment of procedures and work practices for safe operating and maintenance activities.
19. Training for all employees to reach and maintain proficiency in safe work practices and the skills and knowledge necessary to perform theirjob.
20. Demonstrations and documentation of skill proficiency prior to assignment to independent work, and periodically thereafter.
21. Programs designed to assure that employees in safety criticaljobs are fit for duty and are not compromised by external influences, including alcohol and drug abuse.
22. Provisions that contractors either have programs for their own employees consistent with applicable sections of this Code or be included in the member company's program, or some combination of the two.
Glossary
This Code uses key terms in a context that may be broader than their associated regulatory definitions. However, adherence to this Code does not relieve a company of the obligation to meet Federal, state and local regulatory requirements.
Process Safety - The application of management and engineering principles to prevent fires, explosions and accidental chemical releases at chemical process facilities.
Sound Engineering Practice The application ofmandatory codes and standards supplemented by the use of voluntary codes, standards and guidelines, tempered by professional judgement
Safety Critical Jobs. Jobs, activities and tasks, ifimproperly performed, that have the potential to significantly increase the risk of a fire, explosion or accidental chemical release.
Accidental Chemical Release Unplanned, sudden releases of chemicals from manufacturing, processing, handling and on-site storage facilities to the air, water or land. It does not include permitted or other releases.
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Responsible Care: A Public Commitment
SAMPLE
CHEMICAL MANUFACTURERS ASSOCIATION MEMBER SELF-EVALUATION FORM
PROCESS SAFETY CODE OF MANAGEMENT PRACTICES
Member Company Name:_______________
Responsible Care Coordinator Name- .... Address:
Telephone ( ) Number offacilities subject to code
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i^ACUiWC4 *99
S4WPLE
. PROCESS SAFETY CODE OF MANAGEMENT PRACTICES
Instructions:
1. Under the Responsible Care Initiative, eaeh member company will submit a Self-Evaluation form annually to CMA.
2. Indicate on the cover page the number of member company facilities subject to the Code. Each company must report the implementation category for all facilities subject to the Code on this form.
3. For each Management Practice on the following four pages, indicate the number of facilities that have attained eaeh implementation category. Eaeh facility should appear in only one milestone category per Management Practice. The total number of facilities subject to the Code should equal the number of facilities across all six implementation categories for each Management Practice.
4. Only subject facilities owned or operated as ofthe reporting date should be included,
fi. The implementation categories are:
Category NA Category EV . Category DP Category IA Category PP Category RI -
No action. Ifno action taken because the management practice is not applicable, please explain. Evaluating existing company practices against the Management Practice. Developing plan to implement Management Practice. Implementing action plan Management Practice in place. Reassessing Management Practice implementation.
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Process Safety Code 01 Management Pracuaes November 21. 1991 -- Page 3
MiTr,f*m,nf Practice
S&flrlPLE
r tfgnri<Ni
Management Leadership
NA EV DP IA PP RI
1. Leadership by senior management through policy, participa tion, communications and resource commitments in achieving
continuous improvement of performance.
Comments on Category NA:_______________ _____________
2. Clear accountability for performance against specific goals for continuous improvement
Comments on Category NA:
3. Measurement of performance, audits for compliance and im plementation of corrective actions.
Comments on Category NA.*
4. Investigation, reporting, appropriate con active action and fol low-up of each incident that results or could have resulted in a fire, explosion or accidental chemical release.
Comments on Category NA:
5. Sharing of relevant safety knowledge and lessons learned from such incidents with industry, government and the community.
Comments on Category NA:
Catofory KA CUtfory KV Calofory DP
Category IA Catafoty PP Category K1
Wo aetlaa. Ih aetlaa Uka >hwi tfca
pnctlca la sot ippItUU, phut upUi.
bthtdai aaledag ctopuy ptmcdcoa agalaat tfca Maaagoaaat PncSta.
'
Dmbpla|pUi ta Impliieanl Kaaagamaat PtacUaa.
lapliaailii mSm ptsa
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timiiiln llaaa|Mt fticSat hwplmatfaa.
Sk Log054.
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CUCfflTlff
NA EV DP IA PP R1
6. Use of the Community Awareness and Emergency Response (CAER) process to assure public comments and concerns are considered in design and implementation ofthe facility's process safety systems.
Comments on Category NA:___________________ _________
Technology
7. Current, complete documentation ofprocess design and operat ing parameters end procedures.
Comments on Category NA:________
8. Current, complete documentation ofinformation relating to the hazards of materials and process technology.
Comments on Cateeorv NA:
9. Periodic assessment and documentation ofprocess hazards, and implementation of actions to minimize risks associated with chemical operations, including the possibility ofhuman error.
Comments on Cateeorv NA:
10. Management of changes to chemical operations to maintain or enhance the safety originally designed into the facility.
Comments on Catesorv NA:
CutfoyM Catsgary gV Cstsgsry Of Cstsgery IA Csts(7 W Cstsgoiy K1
Page 66 of 98
Us acdss. ff as setlsa tsksa liemi the >s|aiswt pnetice U ast eppMcshM. ylsass eipMta.
Bvslastlag uSstiag ctmpuj practical agaiaat the Maa|--snt Practice.
Develeplag plan ta tepleraeat Maaegemeat Fraadaa.
haplemeadag actlsa pica
-
Meaegemeat Practice ta pisas
Prancering Maasgemeat Practice hwpl--icetctlca.
OS* 108052
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Process Safety Code of Management Practices November 21. 1991 -- Page S
SAMPLE
Cttraorie*
Facilities
NA EV DP 1A PP RI
11. Consideration and mitigation of the potential safety effects of expansions, modifications and new sites on the community, environment, and employees.
Comments on Category NA:
12. Facility design, construction and maintenance using sound
engineering practices consistent with recognized codes and
standards.
'
Comments on Category NA:
13. Safety reviews on all new and modified facilities during design and prior to start-up.
Comments on Category NA:
________________
14. Documented maintenance and inspection programs that en sure facility integrity.
Comments on Category NA:
15. Sufficient layers ofprotection through technology, facilities and employees to prevent escalation from a single failure to a cata strophic event.
Comments on Category NA:
.
Caugwym Catayry gV
CMfeyV CatagaryU Catagory Catagary B2
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a<M|tMt rraettea la ySaaa. Uniiiiiliil Maaigamaat MmSm laijilwftlaa
-DSW 108053
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SAMPLE
CatxnrK
NA EV DP IA PP RI
16. Provision for control of processes and equipment during emer gencies resulting from natural events, utility disruptions and other external conditions.'
r,,mm*nt* on Categoi ry NA:
Personnel
17. Identification of the skills and knowledge necessary to perform each job.
Comment* on Category NA:
....................
18. Establishmentofproceduresandwoikpraetieesforsafeoperat-
ing and maintenance activities.
Comment* on Category NA:
19. Training for all employees to reach and maintain proficiency in safe work practices and the skills and knowledge necessary to perform their job.
Comment* on Category NA:
20. Demonstrations and documentation of drill proficiency prior to assignment to independent work, and periodically thereafter.
Comments on Category NA:
Category KA Category ZW
Category DP Catagary IA Catagary PP Catagary 11
Raaetlae. r~T r-r~a t~*--i I rian r>i grant purtln li ait >rrTT~~*~`~ T*--------------T*`*~
Ereleattag arteh| ooapeay piaatlcaa ogotsot tfca MasagaMaet Piatdra.
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ImpIoaaasUsg aetiae plaa
Maaagaaaat Practice la plaaa.
Xaaaaaaatag Maaagamaat Praetlca faaplaaaatatlaa.
\.0 805*
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November 21. 1991 --Page 7
SAMPLE
Citcgnriffi NA EV DP LA PP RI
2L Programs designed to assure that employees in safety critical jobs are fit for duty and are not compromised by external influences, including alcohol and drug abuse.
Comments on Category NA:
1
I 1
22. Provisions that contractors either have programs for their own employees consistent with applicable sections ofthis Code or be included in the member company's program, or some combine* tion of the two.
Comments on Cateeorv NA:
UtqoiT M
Catagary EV CUigwr OP Category1A Category IV Category U
l*a utiM. V as actloe takas >w the maaageaast practice U ast sppSeahic, pi---- crpUhi Cvalaadag aaiaflsg ceapaayprmctlcaa agalaat tbs **ianiint ftictie*. Dcrolepiaf plaa U Implsa-st Maaagamast Practise. Imp!--leafing sctlsa plaa Kaaagmcst Practice la pleas. Iiiuwitnl Maaagaaant Practice lmnlaa-a*i*f-a
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Process Safety Code of Management Practices Questions and Answers
Management Leadership
1. Q: How does one define senior management?
A: Senior management is that level that has (he authority to establish policies and authorize expenditures to implement them. As used in this Code, this probably includes plant managers and above.
2. Q: What is meant by participation by senior management?
A: Participation in this context refers to activities which convey and reinforce commitment and leadership as well as support the implementation of policies and procedures.
3. Q: Is it necessary to have a written process safety policy?
A: Yes.
4. Q: What parameters can be used to measure process safety performance?
A: Each company should establish its own methods of measurement. Counts of unwanted incidents, frequency rates, property loss statistics, audit violations, permit violations, risk reviews and completion of training are a few examples.
5. Q: How should one define the type ofincident that should be investigated?
A: There is no single standard which defines the type of incident or near-miss to investigate. Management should establish a formal procedure to investigate those uncontrolled events which have potentially serious consequences.
6. Q: What should be done after each incident or near-miss investigation?
A: Corrective actions orfollow-up should be identified, carried outand communicated as appropri ate within the company.
7. Q: What kind ofknowledge and lessons should be shared?
A: Knowledge and lessons which can benefitothers because oftheirgeneral applicabilityor novelty or unusualness. Member companies may establish procedures to promote sharing consistent with proprietary and legal considerations.
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8. Q: How much input do you envision our industry receiving from the public sector?
A: The CMA fully supports the concepts ofworking with local communities to listen to their views and concerns and to considerthem in plant safety systems. The intent is to discuss major process additions and new grass-roots construction as opposed to minor plant changes. Individual companies are responsible for the safe design and operation of facilities; that responsibility cannot be shared with the public. Itis intended thatpublic concerns be considered in design and operations of the facility. The CAER network provides a useful vehicle to accomplish this.
Technology 9. Q: What type of documentation of process design and operating parameters should exist?
A operating unit should have up-to-date safety related information that contains the design basis and procedures, (e.g., process flowsheets, piping and instrument diagrams or engineering flow diagrams, vessel drawings, electrical area classifications, safetyvalve capacity information and operating manuals). The documents will serve as the back bone for employee training, hazard evaluation and process modifications.
10. Q: What is meant by operating parameters?
A Operating parameters are the ranges of conditions (eg. temperature, pressure and flow composition) within which a unit is designed to operate. Within that range, a unit is expected to operate without any problems. For example, the safe operating parameter for a reactor temperature during exotherm might be 70 degrees TMniinniH to 130 degrees maximum. Operating outside the range could cause instability in the reaction -- runaway temperature if above, potential brittle fracture if below.
11. Q: What are some ofthe types ofinformation needed to define the chemistry?
A- Each reactant and product should have a material safety data sheet(MSDS). Chemical reaction kinetics and acute toxicity should be known and understood. Reactive chemical performance upon mixing various ehcmicals in different proportions should be documented. Waste stream* should be included as well as reactants and products.
12.Q: What type of procedures should be maintained?
A- Generally, all routine jobs or tasks with process safety implications should have written stepby-step instructions. These procedures should capture the experience base ofthe knowledgeable experts. The protective equipment and employee concerns should be incorporated in the procedures. Also, emergency procedures must be dear and unequivocal
13. Q: What is the difference between documentation covered in practice 7 versus that included in practice 8?
A* Number 7 refers mainly to design operating information, while number 8 specifically addresses the hazards associated with the unit being evaluated.
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' 14. Q: Does the reference in the Code to rick imply that we will be required to perform quantitative risk assessment* on all our plants?
A: No. Qualitative analytic alone should be sufficient to satisfy process safety analysis objectives in most eases. In any ease, qualitative analysis should be considered prior to performing numerical frequency or consequence calculations.
15. Q: What does periodic assessment of process hazards mean in the technology element?
A: Each member company should establish its own review frequency based on inherent hazards, operating experience, rate oftechnology change and other factors. Typical review frequencies range from three to seven years. Under very special circumstances, review frequency may be as short as one year.
16. Q: What is meant by "management of change"?
A: "Management ofchange" means having management systems in place that ensure the original
safe design of the
u maintained and all changes, including minor modifications, are
properly reviewed, recorded and communicated
17. Q: What changes should be covered?
A: All changes except like for like substitutions. Examples include hardware, procedures, raw materials, operating conditions, throughput, employee, software and control mode.
18. Q: There does notseem tobe a deardistinction between Technology and Facilities-shouldn't these two sections be combined?
A: While it is true that the two sections are closely related and interdependent. Technology (i.e.,
chemistry and know-how) and Facilities (Le^ equipment and hardware) each deserve an
independent focus as related to process safety.
.
19. Q: Should the community be consulted when considering potential effects of a new rite or new
installation?
-
A: Yes, using principles of the CAER process.
20. Q: Does this mean the community has approval or rejection authority over our projects?
A: No: It means that we should identify and respond to community concerns.
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September 11. 1990 -- Page 4
.
21.Q: Choosing a new plant cite involves many complex considerations. Can we realistically expect to completely satisfy all interests?
A: Possibly not, bat the Responsible Care Guiding Principles require health, safety and the environment to be priority considerations and such issues must be adequately resolved.
22. Q: Does the Code cover concerns about sabotage or terrorism?
A: Such issues are not intended to be within the scope ofthe Code. However, good practice in site selection and planning will consider such general security issues as buffer zones, fencing, lighting, entrance gates and security surveillance. Also, mitigation and emergency response measures can help minimise consequences ofhostile acta
23. Q: Does "sound engineering practice" extend beyond mandatory codes and regulations?
A: In many cases, yes. While government codes and regulations may establish minimum legal requirements for plant design, operation and maintenance, member companies ere expected to use qualified professionals to identify and apply other engineeringpractices (such as contained in many non-mandatory or consensus standards or codes) as may be necessary to fulfill our safety commitment to employees and the community.
24. Q: Are "Safety Reviews" as prescribed in practice 13 differentfrom "Process Hazard Assessments" as prescribed in practice 9?
A: Yes. "Process Hazard Assessment" is done during the process design stage and periodically thereafter. It focuses on the hazards inherent to the process and measures to control these hazards. "Safety Reviews" use "Process Hazard Assessment" as a starting point and focus on the physical installation to assure that itis in accordance with design and is safe to start-up and operate.
25. Q: Shouldn't Safety Reviews go beyond simple field inspection?
A: Yes. Safety Reviews may include such things as testing equipment, controls, control logic, interlocks, "water runs" ete., prior to operation with hazardous materials. In addition, such reviews should also confirm that process documentation and procedures are in place and that operators have been trained.
26. Q: Doesn't a "Preventive Maintenance Program" meet the requirement of practice 14?
A: To meet the intent of this code practice, the preventive maintenance (PM) program must go beyond operating reliability and economic considerations and address all potential failures which, while possibly extremely unlikely, could impact process safety. A program to "ensure facility integrity" must search outhidden deterioration and flaws that can result in sudden end unexpected failure that can impact process safety.
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27. Q: What are tome examples that could be included in a PM program to satisfy practice 14?
A: Metallurgical examinations for stress corrosion cracking, nondestructive acoustic testing, compressor vibration monitoring, thickness measuring for erosion or corrosion on key parts of pressure vessels and pipelines, verification of bolt and damp material of construction and qualify, reliability of critical instruments and operation of safety valves are examples.
28. Q: Shouldn't a hierarchy be considered in applying 'layers of protection"?
<
A: Normally technology should be applied first, choosing an inherently safe or less haxardous process wheneverpossible. Then hardware, safetyfactors,redundantcontrols, failure detection systems, etc., should be applied. Finally, emergency procedures and employee training should complement the process and hardware design.
29. Q: How many layers constitute "sufficient layers of protection"?
A: There is no absolute answer to this question. The number of levds needed depends on the likelihood ofan initial failure, the nature ofthe consequences and whether additional levels of protection will materially improve safety. Layers of protection include more than redundant equipment. They may include process techniques, instrumentation and hardware, operating procedures and operator training.
30. Q: What is meant by "external conditions"?
A: By external conditions we mean anythingthat is beyond the direct and immediate control ofthe process operator. An example might be an evacuation order for your plant caused by a fire or toxic release from a neighboring plant as well as an upset or incident in an adjoining process unit.
Personnel
31. Q: We train our employees thoroughly; why is it necessary to also demonstrate their proficiency?
A: Even with the best employee trainingprograms, people learn at different rates and comprehen sion. An actual demonstration is the only way ofbeing sure that each individual has grasped essential concepts or skills Demonstrations can involve written tests and/or havingthe trainee show a qualified observer how they would do a job.
32. Q: Do procedures and work practices have to be documented?
A: Generally, yes. Procedures typically require proper execution of several stages. Documented procedures help assure that a critical action is not overlooked and that the procedure is carried out consistently by everyone.
33. Q: Does the code require that employees be screened for alcohol and drug abuse?
A: No. The Code requires programs designed to assure fitness for duty.
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Proceea Safety Code of Management Practices September 11. 1990 -- Page 6
34. Q: What kinds ofjobs are safety-critical?
A: A position is safety-critical when it involves tasks which, if not performed prooerly, can significantly increase the likelihood of a fire, explosion, or accidental chemical release.
35. Q: What is meant by `external influence"?
A: External influenza indude abuse of alcohol or drugs, but the terms also refers to any factor which mightimpairjudgement, attention or general capacity to perform ajob safely. Examples indude physical impairment, emotional stress, and stress from too much overtime work.
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Responsible Care: A Public Commitment
EMPLOYEE HEALTH AND SAFETY CODE OF MANAGEMENT PRACTICES
PURPOSE
The goal of the Employee Health and Safety Code ofManagement Practices is to protect and promote the health and safety of people working at or visiting member company work sites.
To achieve *hi goal, the Code provides ManagementPractices designed to continuously improve work site health and safety. These practices provide amultidisciplinarymeans to identify and assess hazards, prevent unsafe acts and conditions, maintain and improve employee health, and foster communication on health and safety issues.
Implementation ofthe Employee Health and Safety Code, together with ether Codes ofManagement Practices, can enable member companies to operate in a manner that further protects and promotes the health and safety of employees, contractors, and the public, and protects the environment.
RELA TIONSHJP TO GUIDING PRINCIPLES
Implementation of the Code helps achieve several of the Responsible Care* Guiding Principles:
I To recognize and respond to community concerns about chemicals and our operations.
I To make health, safety, and environmental considerations a priority in our planning for all existing and new products and processes.
I To operate our plants and facilities in a mannerthat protects the environment and the health and safety of our employees and the public.
I To extend knowledge by conducting or supporting research on the health, safety, and environmental effects of our products, processes, and waste materials.
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MANAGEMENT PRACTICES
Each member company shall have an ongoing occupational health and safety program that includes:
Program Management
1. Commitment by all levels ofmanagement to protecting and promoting the health and safety of people working at or visiting member company work sites through published policies; accountability for implementation; and provision ofsufficient resources, including qualified health and safety personnel
2. Opportunities for employees to participate in developing, implementing, and reviewing health and safety programs.
3. Provisions, including selection criteria, to confirm that on-site contractors' programs are consistent with applicable Management Practices ofthis Code.
4. Written, up-to-date health and safety programs and procedures appropriate to the facility.
5. Means to verify that health and safety programs and procedures are effective and that actual practices are consistent with these programs and procedures.
6. Systems for maintaining records and analyzing data to evaluate health and safety perforznance, determine trends, and identify areas for improvement.
identification and Evaluation
7. Methods to identify and evaluate potential health and safety hazards in planned or existing facilities, including facilities to be modified.
8. Exposure assessments and safety analyses to evaluate health and safety hazards to employ
ees from processes; equipment; potentially hazardous chemical, physical, or biological
agents; or other work site conditions.
..
9. Health assessments to determine employee medical fitness for specific job tasks.
10. Employee occupational medical surveillance programs tailored to work site hazards.
Prevention and Control
1L Mechanisms for reviewing the design and modification offacilities andjob tasks, taking into account the following hierarchy of controls: inherent safe design, material substitution, engineering controls, administrative controls, and personal protective equipment.
12. Systems to verify that health and safety equipment is properly selected, maintained, and used.
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13. Preventive maintenance and housekeeping programs to maintain the safety of facilities, tools, and equipment.
14. Timely investigation of work site illnesses, injuries, and accidents; corrective actions to prevent recurrence; and evaluation of the effectiveness of corrective actions taken.
15. Security procedures and systems to control entry and exit of personnel and materials at the work site and restricted areas.
16. Provisions for emergency medical assistance for people at work sites.
Communications and Training 17. Communication ofhealth and safety information that is relevant to specificjob tasks and the work site. 16. Health and safety training programs, including documentation of these programs, and methods to evaluate the effectiveness of both training and communications activities.
INDUSTRY TREND DATA
To identify industry trends, each company shall report to CMA, or its designated agent, occupational injuries and illnesses, as specified in CMA's Occupational Injury and Illness Reporting Program.
RELATIONSHIP TO OTHER CODES OF MANAGEMENTPRACTICES
This Code complements, and should be implemented in conjunction with, current and future Codes of ManagementPractices, especially those elements ofthe CAER Code involvingemergency response, the Process Safety Code involvingtrainingofemployees in theirjob functions, and the ProductStewardship Code involvinghealth, safety, and environmental information, and employee education and product use feedback.
MEMBER SELF-EVALUATION
Each member company shall report annually to CMA, or its designated agent, the implementation category attained for each Management Practice in this Code. The reports should be submitted on the member self-evaluation form provided.
RESOURCE GUIDE
A separate resource guide is available to assist member companies in implementing the Code.
The Reaponaibla Carr* Employee Health A Safety Cade of Uanagcmeat Practical waa approved by CMA'a Board of Director* on January 14.1092
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Responsible Care: A Public Commitment
EMPLOYEE HEALTH AND SAFETY CODE OF MANAGEMENT PRACTICES
MEMBER SELF-EVALUATION FORM
Member Company Name*.
Responsible Care* Coordinator Name:. Address:.
Telephone: I____ 1
Number of facilities subject to the Employee Health and Safety Code:.
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EMPLOYEE HEALTH AND SAFETY CODE
MEMBER SELF-EVALUATION FORM
Instructions for the Company Responsible Cere* Coordinator
1. This form is to be submitted annually to CMA by each member company.
2. Indicate on page 1 the number ofyour member company's facilities that are subject to the Code. Each company must report the implementation stage for all facilities subject to the Employee Health and Safety Code on this form.
3. For each Management Practice on the following pages, indicate the number offacilities that have attained each implementation category. Each facility should appear in only one implementation category per ManagementPractice. Identify the current implementation category for each ofyour facilities at the time you complete the form.
4. For the Industry Trend Data, reportthe previous calendar year's cumulative occupational injuries and illnesses. Occupational injuries and illnesses should be reported on a company wide basis as specified by CMA's Occupational Injury and Illness Reporting (OER) Program.
5. Only subject facilities owned or operated as of the reporting date should be included.
6. The implementation categories are:
Category NA - No action. If no action token because the Management Practice is not appli cable, please explain in space marked ^comments."
Category EV - Evaluating existing easnpanypractices against the Management Practice. Category DP - Developingplan to implement Management practice.
Category Li - Implementing action plan. Category PP - Management Practice in place. Category PI - - Reassessing Management Practice isnplementmtion.
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EMPLOYEE HEALTH AND SAFETY CODE OF MANAGEMENT PRACTICES
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Management Practices
Categories
NA EV D* IA PP HI
1. Commitment by all level* of management to protecting and promoting' the health and safety ofpeople working at or visiting membercompany sites, through: publishedpolicies:accountabil ity for implementation; and provision of sufficient resources, including qualified health and safety personnel
Comments on Ceteforv NA-
2. Opportunitiesfor employees to participate in developing, imple menting, and reviewing health and safety programs.
Comments on Cale?nrv NA-
3. Provisions, including selection criteria, to confirm that on-site contractors' programs are consistent with applicable Manage ment Practices ofthis Code.
Comments on Cateaorv NA:
4. Written, up-to-date health and safety programs and procedures appropriate to the facility.
Comments on Category NA?
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Management Practice*
Categories
NA EV DP 1A PP HI
5. Means to verify that health and safety programs and procedures are effective and that actual practices are consistent with these programs and procedures.
Comments on Category NA: '
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6. Systems for maintainingrecords and analyzing data to evaluate health and safety performance, determine trends, and identify areas for improvement.
Comments an Category NA:
7. Methods to identify and evaluate potential health and safety hazards in planned or existing facilities, including facilities to be modified.
Comments on Cateforv NA;
6. Exposure assessments and safety analyses to evaluate health and safety hazards to employees from processes; equipment; poten tially hazardous chemical, physical, or biological agents; or other work site conditions.
Comments on Category NA:
9. Health assessments to determine employee medical fitness for specific job tasks.
Comments on Category NA:
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Management Practice*
Categories
_______________________________________________ ___________ _ NA
10. Employee occupational medical surveillance programs tailored to work site hazards.
Comments on Category NA-
1L Mechanisms for reviewing the design and modification offacili ties andjob tasks, takinginto aeeount the foDowinghierarchy of controls: inherent safe design, material substitution, engineer* ing controls, administrative controls, and personal protective equipment.
Comments on Category NA:
12. Systems to verify that health and safety equipment is properly selected, maintained, and used.
Comments on Category NA:
13. Preventive maintenance and housekeeping programs to main tain the safety offacilities, tools, and equipment.
Comments on Category NA:
14. Timely investigation of work site illnesses, injuries, and inci dents; corrective actions to prevent recurrence; and evaluation of the effectiveness of corrective actions taken.
Comments on Category NA:
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Management Practice*
Categories
NA tV DP IA PP ftl
15. Security procedures and systems to control entry end exit of personnel end materials at the work site and restricted areas.
Comments on Category HA:
16. Provisions for emergency medical assistance for people at work
sites.
.
Comments on Category NA;
17. Communication ofheahh and safetyinformation thatis relevant to specific job tasks and the work site.
Comments on Category NA;
18. Health and safety training programs, including documentation of these programs, and methods to evaluate the effectiveness of both training and communications activities.
Comments on Category NA;
INDUSTRY TREND DATA
Occupational injuries andforthe previous calendaryearwere reported as specified
in CMA's Occupational Injury and Illness Repenting Program.
Yes____
No____
"
If no, please explain:____________________________________________________________
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Page 68 of 98
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QUESTIONS AND ANSWERS
EMPLOYEE HEALTH AND SAFETY CODE OF MANAGEMENT PRACTICES
Throughoutits development, theEmploy#* Health andSafety CEHS) Codewasreviewed regularly by CMA't Health and Safety Committee, Engineering and Operations Committee, and Responsible Care*CoordinatingGroup. An earlydraftoftheEHSCodewasreviewedbymembereompanies through written comments and an open meeting, and member eompanies conducted a second review ofthe draft EHS Code with their employees. In addition, the draft EHS Code was reviewed periodically by the Responsible Care* Public Advisory Panel
During these reviews, the following questions were frequently asked about the EHS Code of Management Practices:
1. Does the EHS Code cover all aspects of an employee's health and safety?
Answer: The EHS Code is restricted to those aspects ofan employee's health and safety that are affected by his orher employmentin the chemical industry. TheEHS Code addresses occupational health and safety and does not address employee wellness or cff-the-job safety.
2. Does the EHS Code include visitors and all contractor operations?
Answer: The EHS Code covers all visitors and contractor employees who enter a member company's work site. Visitors should be protected from hazards they may encounter while on the work site. All contractors should have health and safety programs for their employees that are appropriate forthe hazards encountered in their contractedjob tasks and that are consistent with applicable management practices of the EHS Code. Contract manufacturers, or tollers, are addressed in the Product Stewardship Code.
3. Does the EHS Code require employee participation at work sites at which employees are represented by a union?
Answer: The objective of the EHS Code is to encourage member companies to fully involve employees in safety and health activities. However, at facilities at which employees are represented by a union, negotiations concerning ruch employee participation may be required. In the contract negotiation process, member companies should make s good-faith effort to address opportunities for employee participation.
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4. What is CMA's Occupational Injury and Illness Reporting (OUR) Program?
Answer: CMA's OIIR Program serves as a basis for awarding the annual Lammot Du Pont Safety Awards recognizing sustained achievement by CMA member companies in reducing workplace injury and illness rates. Each participating company submitt its injury and illness data, as reported on the OSHAForm 200, based on guidelines issued bythe U.S. Bureau ofLabor Statistics (BLS).
4
6. Are contractor employees included in the OQR Program?
Answer. At this time, contractor employees are not included in the CMA OUR Program, unless the company directly supervises their day-to-day activities. Current BLS guidelines require reporting of occupational injuries and illnesses by individual employers besed on Standard Industrial Classification (SIC) codes. Both CMA and OSHA are considering revisions to the reportingguidelines that would consolidate rite reporting ofoccupational injuries and illnesses for a single work site, without regard to the SIC code ofthe employer.
6. Does the EHS Code address subetanee abuse in the workplace as part of sueeasing medical fitness for specificjob tasks?
Answer. Substance abuse is addressed by the Process Safety Code in Management Practice 21: "Programs designed to assure that employees in safety-critical jobs are fit for duty and are not compromised by external influences, ineluding alcohol and drug abuse.*
7. Does the EHS Code require job tasks to be evaluated for physical requirements?
Answer. Job tasks should be evaluated to determine the specific physical abilities associated with a task. An employee's abilities should be evaluated using medical criteria before being assigned to a job task with specific physical requirements. For example, employees should be medically evaluated to determine their ability to wear a respirator before being assigned to job tasks requiring the use of a respirator.
6. Does the EHS Code require member companies to provide annual medical examina tions to all employees aa part of an occupational medical surveillance program?
Answer. No. .Occupational medical surveillance programs should provide appropriate, targeted medical assessments to those employees exposed to specific hazards. For example, regular spirometry examinations to assess lung function should be offered to employees exposed to an agent known to affect lung function.
9. Does the EHS Code require member companies to assess the effect of exposure* to chronic hazards on the health of employees?
Answer. As s part of maintaining records and analyzing data for trends, member companies should assess the long-term health experience oftheir employees in relationship to exposures to chronic hazards. Chronic hazards include, for example, long-term exposures to carcinogens.
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Product Stewardship Booklet for the Code of Management Practices
The code's management practices are grouped into three categories, described as
follows:
-
Management Leadership and Commitment contains Management Practices 1-3. These practices serve to give direction, provide resources, set priorities, and establish
responsibilities within your company that provide an appropriate atmosphere and founda tion tor successfully implementing product stewardship.
Information and Characterization includes Management Practices 4 and 5. These address the need to continually increase the body ot Knowledge surrounding chemical products in order to improve hazard identification and risk characterization at every stage in a product's fife.
As the cornerstone of product stewardship. Management Practices 6*12 are categorized as Risk Management practices, which work together to manage risks at every stage of a product's life. Some of these management practices are the most chaflenging in ihe Code because they extend the risk management process beyond traditional boundaries to consider risks beyond the point of sale.
Management practices in the first two categories provide the foundation for conducting the risk management practices in the third category. The ability to implement each management practice, therefore, refies upon the successful implementation of previous practices, with the successful development and implementation of product stewardship progressing from a planning and resource allocation to an information collection phase,
and finally to action-oriented, risk management activities.
Purpose and Scope
The purpose of the Product Stewardship Code of Management Practices is to make health, safety and environmental protection an integral part of designing, manufacturing, marketing, distributing, using, recycfing and disposing of our products. The code pro vides guidance as well as a means to measure continuous improvement in the practice of product stewardship.
The scope of the code covers all stages of a product's life. Successful implementation is a shared responsibility. Everyone involved with the product has responsibilities to address society's interest in a healthy environment and in products that can be used safely. All employers are responsible tor providing a safe workplace, and aO who use and handle products must follow safe and environmentally sound practices.
The code recognizes that each company must exercise independent judgment and discretion to successfully apply the code to its products, customers and business.
i
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THE PRODUCT STEWARDSHIP CODE
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Relationship to Responsible Care* and Guiding Principles
Implementation of the code promotes the achievement of several of the Responsible Care* Guiding Principles:
to make health, safety and environmental considerations a priority in our planning tor ail existing and new products and processes:
to develop and produce chemicals that can be manufactured, transported, used and disposed of safely:
< to extend knowledge by conducting or supporting research on the health, safety and environmental effects of our products, processes and waste materials;
to counsel customers on the safe use, transportation and disposal of chemical products;
to report promptly to officials, employees, customers and the public, information on chemical-related health or environmental hazards and to recommend protec tive measures;
to promote the principles and practices of Responsible Care* by sharing experi ences and offering assistance to others who produce, handle, use. transport or dispose of chemicals.
This code complements, and should be implemented in conjunction with, current and future Codes of Management Practices. Chapter 3 discusses the Product Stewardship Code's relationship to the other existing codes.
Management Practices
Management Practice 1
LEADERSHIP: Demonstrates senior management leadership through written policy, active participation and communication.
The objective of this management practice is to set the driving force for the Product Stewardship Code. To this end. senior management must first adopt a policy that reflects the company's vision of product stewardship. Thispolicy should state clearly how senior management expects product stewardship to be managed within the com pany.
To be effective, the policy should emphasize that product stewardship, lice quality and safety, must be woven into the company's culture. It also should be clear that the commitment is an ongoing, tong-term part of the company's operations and business.
Finally, if the new policy represents a change in the way of doing business, it should be dear that a change in behavior is expected. In some companies, a separate written product stewardship policy may be effective. In others, a broader health, safety and environmental (H.S&E) policy that incorporates the principles of product stewardship may be more appropriate.
However, a policy alone is not enough. The words of a policy must be reinforced by actions and behaviors that continuously reaffirm the goals senior management has set Senior management is responsible for conveying throughout the organization its involve ment with, and support of. product stewardship--especially to the next level of manage-
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merit and encouraging it to do the same. (Management Practices 2 and 3 tocus on some o< the visible signals - tor example, goals, performance measurement and resource allocation).
Management PraCtiCC.2
ACCOUNTABIUTY snd PERFORMANCE MEASUREMENT: Establishes goals and responsibilities for Implementing product stewardship throughout the organiza tion. Measures performance against these goals.
One of the key ways senior management can convey the importance of product steward ship is by establishing it as a priority in business planning and individual performance planning. The objective is to develop a process that will result in continuous improve ment through goals that are well-defined, achievable and measurable. Similarly, indi vidual responsibilities should be clear and consistent
Management Practice 3
RESOURCES: Commits resources necessary to Implement and maintain product stewardship practices.
The commitment of resources, both human and financial, is a critical signal that manage ment can send to show its commitment to product stewardship practices and is a vital component for some implementation activities. Undoubtedly, resources will vary from company to company. However, in all cases, the commitment of resources should be consistent with product stewardship implementation plans and sufficient to support continuous improvement
Management Practice 4
HEALTH, SAFETY and ENVIRONMENTAL INFORMATION: Establishes and main tains Information on health, safety and environmental hazards and reasonably foreseeable exposures from new and existing products.
Just as Management Practice 1 is the driving force for the Product Stewardship Code. Management Practice 4 is the foundation. The objective of Management Practice 4 is to
establish a knowledge base of human and environmental hazards and reasonably foreseeable exposures and, once established, to maintain it Underthis practice, compa nies gather information to support the system that characterizes a product's risk (Man* agement Practice 5) and. ultimately, the system that develops the methods to manage that risk (Management Practice 6).
Initially, some companies may establish their knowledge base by developing information; others may do so by collecting and compiling available information. However, all compa nies should have a process to continuously gather relevant product information and to review existing information to determine if it is accurate, current and complete.
Sources of information may indude pubfished, unpublished and/or internally generated scientific reports on health, safety and environmental effects and exposures. Generally, the types of information could cover animal or human toxicity, ecotoxidty and chemical and physical properties that affect exposure or the environmental impact. In many cases, exposure information is not directly available but may be estimated with product use information.
Information on a product's handling, use and reasonably foreseeable exposures in research, development, manufacturing, transport, storage, packaging and disposal may
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be obtained by a number of means. These could include surveys ot customers ana otner product receivers, technical reviews or visits to customers, and/or observations reported by sales and marketing personnel.
Management Practice s
PRODUCT RISK CHARACTERIZATION: Characterizes new and existing products with respect to their risk using Information about health, safety and environmental hazards and reasonably foreseeable exposures. Establishes a system that ini tiates re-evaluation.
This practice has two objectives. The first is to use the information gathered in Manage ment Practice 4 to develop a thorough understanding of the product's risk. This charac terization may be either quantitative or qualitative. The second objective is to establish a system that triggers re-evaluation, whether upon receipt of new information or upon periodic, scheduled review.
A product may bq characterized as a single entity or it may be characterized in a group of products based on similar uses, compositions or physical properties. Product risks may vary with different uses or exposures.
The time frame for re-evaluation may vary from product to product. Triggers for such re evaluations might include significant new hazard or exposure data, significant new use or misuse information as it becomes known or a substantial increase in sales volume, suggesting new uses or markets.
Management Practices
RISK-MANAGEMENT SYSTEM: Establishes a system to Identify, document and Implement health, safety and environmental risk-management actions appropriate to the product risk.
The objective of Management Practice 6 is to establish a system for identifying and implementing risk-management actions. Risks involved in the production and use of chemicals can be managed and controlled if each company takes the basic information on a product's risk (Management Practice 4), characterizes It (Management Practice 5) and then implements a series of risk management actions (Management Practice 7 through 12). These risk management actions are a result of a conscious weighing of technical, ethical, societal and business issues surrounding a product Actions taken as a result can range from no action, to provkfing MSOSs and labels, to product reformula tion or repackaging, to removal of the product from a market
The management practices that follow. Management Practices 7 through 12, are specific areas of company operations that warrant discussion and special emphasis.
Management Practice 7
PRODUCTand PROCESS DESIGN and IMPROVEMENT: Establishes and main tains a system that makes health, safety and environmental impacts-induding the use of energy and natural resources-key considerations In designing, developing and Improving products andprocesses.
Designing products and processes (or redesigning existing products and processes) with a system to identify health, safety and environmental impacts throughout the product lifecycle is one of tire most effective ways of managing the product risks identified in Management Practice #5. One objective of this Practice is attainment of the preferred
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IIIE PRODUCT STEWARDSHIP CODE
environmental hierarchy: source reduction: reuse: recycling: and disposal. Source reduction includes equipment or technology modifications, process or procedure changes, product reformulation or design, substitution of raw materials, and improve merits in housekeeping, maintenance, training or inventory control.
This Practice also addresses the need for proper energy and natural resource utilizationimportant considerations for reducing potential adverse environmental impacts and achieving sustainable development.
The health, safety and environmental attrfeutes of the product throughout its entire life cycle should be addressed at the beginning, during the concept and design (or redesign) phases. Re-evaluation should occur on a periodic basis or whenever changes to the
product or process are contemplated.
Insights and contributions from employees in all functional areas that may affect health,
safety and the environment should be incorporated into the review. These functional
areas include research and development, manufacturing, distribution, sales and market
ing and regulatory personnel.
'
Management Practlce.8
EMPLOYEE EDUCATION and PRODUCT USE FEEDBACK: Educates and trains employees, based on Job function, on the proper handling, recycling, use and disposal of products and known product uses. Implements a system that encour ages employees to feed back Information on new uses. Identified misuses or adverse effects for use In product risk characterization.
This practice has two parts. The first is to ensure that all employees who are involved with products have the training and education necessary to understand product (and packaging) hazards, proper use, handling, reuse, recycling and disposal procedures. The second is to help ensure that any new information that may alter the way risk is being managed is factored into the risk characterization process on a timely basis (Management Practice 5).
The training and education of employees should be tailored to specific job functions. For example, marketing and sales personnel are in a unique position to know how customers are using products and must be aware of product hazards, reasonably foreseeable exposures, appropriate uses and proper handling procedures. They should be able to identify product deviations and to recognize adverse health or environmental effects. These personnel should be alert to the customer's and the public's comments or percep tions.
It is essential that there be timely feedback of this safety, health or environmental infor mation or concerns into the risk characterization process (Management Practices 4 and 5). This feedback may change the risk management actions (Management Practice 6).
Management Practice 9
CONTRACT MANUFACTURERS: Selects contract manufacturers who employ appropriate practices for health, safety and environmental protection for the operations under contract, or works with contract manufacturers to help them implement such practices. Provides Information and guidance appropriate to the product and process risk to fosterproper handling, use, recycling and disposal. Periodically reviews performance of contract manufacturers.
The objective of this Management Practice is to encourage the use of contract manufac turers who have sound health, safety and environmental practices for the specific opera tions under contract.
SW 108081
'
R Page 95 of 98
WATER_PCB-SD0000021630
THE PRODUCT STEWARDSHIP CODE
The level of involvement will vary according to the product's risk. Activities could inciuae reinforcement of previously provided health, safety and environmental information, additional training, etc. At a minimum, both parties should share any accumulated knowledge that would enhance health, safety and environmental protection.
The "transmittal of appropriate information" acknowledges that while we want customers to pass along H.S&E information, product changes made by the customer may mean that the information originally supplied with the product no longer applies. In these cases, the customer needs to issue information that reflects the current H.S&E informa tion.
Along with Management Practices 9.10 and 11. this management practice constitutes an important outreach component of the Product Stewardship Code. The long-term result of implementing this practice. Bka the other outreach management practices, should result in improved health, safety and environmental performance - not just for CMA member companies but the entire chemical industry.
As with distributors and suppliers, reviews of customers win be commensurate with product risk. However, it is appropriate to expect companies to extend the principles of product stewardship beyond the CMA membership and Responsble Care*partners.
R. Pape 98 of 98
DSU 108084
WATER_PCB-SD0000021631
{{& MONSANTO PLEDGE GUIDELINE
. #1
POLLUTION PREVENTION
The company will work toward the ultimate goal ofensuring zero effect attributable to waste in all media. It will research, design and operate its facilities to minimize the generation ofprocess and nonprocess waste and the potential effect ofchemical releases to the environment. For waste and releases that remain, the company will comply with regulations, while minimizing environmental threat and long-term liability.
KEY RESULTS
Reduce by 90 percent the company's 1987 level of worldwide air emissions of chemicals named by the United States Environmental Protection Agency (USEPA) under Title IH of the Superfund Amendments and Reauthorization Act (SARA Section 313) and chemicals of local concern outside the United States by the end of 1992.
Reduce by 70 percent the company's worldwide SARA Section 313, European Community Priority Pollutant List (EC 129) and carbon monoxide chemical releases to all media and off-site transfers by the end of 1995.
Discontinue the deep-well injection of Resource Conservation and Recovery Act (RCRA) hazardous waste streams and SARA Section 313 toxic chemicals by the end of 1999.
PROGRAM
1.1 Process Waste _
The operating units will integrate into their release reduc tion plans the corporate goal of reducing all toxic and hazardous releases and emission to all media, working toward an ultimate goal of zero effect For reducing releases from processes, the order of preference is source reduction, followed by reuse, recycling or co-product sale, and Anally by incineration or other treatment to reduce the volume and/or toxicity of pollutant streams.
The development and use of technologies that improve
competitive positions will be emphasized.
'
The operating units will integrate into their releasereduction plans the following corporate goals:
Reduce by 90 percent the company's 1987 level of worldwide air emissions of SARA Section 313 chemicals and chemicals of local concern outside the United States by the end of 1992.
Reduce by 70 percent the company's worldwide SARA Section 313, EC 129 and carbon monoxide chemical releases to all media and off-site transfers by end of 1995. The January 1990 SARA 313 and EC 129 lists plus carbon monoxide apply through th< end of the multimedia release reduction program.
An effect-based release reduction target will be establisbe every five years beginning in 1995, working reward an ultimate goal of zero effect. By the end of 1993, a metho and process for an effect-based reduction program for toxic chemicals will be developed.
1.2 Nonprocess Waste
Each facility will maintain an inventory of all nonprocess sources of waste generation, including power generation, office and maintenance operations, general warehouse trash, packaging/shipping materials and similar sources.
MONSANTO COMPANY
CSW 108065
MPG 1, Page 1 c Company Confident
WATER_PCB-SD0000021632
1J Underground Well (Deep-well) Injection
The company will discontinue deep-well injection of RCRA hazardous waste streams by the end of 1999. It will also apply best feasible technology to virtually eliminate the deep-well injection of SARA 313 chemicals. The company's name will not appear on the list of companies malting significant use of injection wells for disposal of SARA chemicals for the reporting year 2000 and beyond. The company will demonstrate progress by achieving in 1996 an 80 percent reduction of injected SARA chemicals against the 1990 base reporting year.
To be prepared for the possibility of mandatory regulations, the company intends to select by the end of 1996 optimal technical strategies for to&l withdrawal from deep wells. This preparation will include studygrade estimates to achieve non-brine, treated surface discharge. All operating units will continue where possible to challenge the technical impediments to total withdrawal from deep wells.
No new uses of deep wells for hazardous or toxic materials are permitted. A "new" use of deep wells is defined as injection of streams from new products or the addition of substances not previously injected at that site. New internal or external uses of deep wells for nonhazardous wastes and nontoxic chemicals will be considered by the Environmental Policy Committee (EPC) only on an exception basis and within the constraints of these guidelines. The economics of any project appropriation request for such use must be based on disposal technology other than the use of deep wells.
1.4 Polychlorinated Biphenyls - "PCB-Free"
All company-owned sites (e.g., warehouses, plants, offices) located in the United States will minimize the potential for releases of polychlorinated biphenyls (PCB) by becoming "PCB-free" of Toxic Substances Control Act (TSCAj-contaminated articles by the end of 1994.
1.5 Land Disposal
Landfill of "acutely hazardous" wastes1 and "incinerables"1 will not be practiced. For hazardous wastes and wastes managed as hazardous, fixation of particularly mobile, persistent or bioaccumulative wastes will be accomplished whenever warranted and
feasible. In making the decision to manage wastes as hazardous, the company will take into account public expectations, emerging trends and worldwide company practice regarding the same or similar wastes.
Contractors hired for land disposal of process wastes will be subject to contracting and assessment requirements (see Pledge Guideline No. 7, Outside Processors). In the United States, the use of off-site hazardous waste landfills will be approved by the Environmental Policy Committee and will be limited in number.
Medical wastes generated at the company's locations will be incinerated prior to land disposal of residues. Assurance of incineration will be obtained via manifests or equivalent documents if manifests are not available.
The use of Monsanto facilities to commercially treat, store or dispose of non-Monsanto wastes is normally discouraged. Any such use or joint ventures (other than in site guest/host relationships) for waste management must be reviewed and approved by the Environmental Policy Committee.
Proposals for land application of process by-products and residues, for beneficial use or disposal, should be guided by the "Monsanto Guidance Document: Land Application of Process By-Products and Residues." The ESHA (formerly EC-201/202) discipline will be followed for such proposals, including 5-year reviews. New applications must be approved by the appropriate Directors of Manufacturing and Environmental operations; the Environmental Policy Committee must approve if beneficial use is not included.
Each company location will maintain a record of both the on-site and the commercial waste treatment, storage and disposal sites it uses.
1.6 Air Emission and Water Release Assessments
The company will conduct and maintain an ongoing assessment of potential human health impacts for selected, routinely emitted air pollutants. It will develop appropriate control strategies to reduce identified, potentially unreasonable risk of harm to human health in surrounding communities. The list of air pollutants to be studied include: a) those listed under Section 112(b) of the U.S. Clean Air Act; b) those for which the
1 As listed in 40 CFR 261.33(e). plus any mixtures containing greater than 5 percent 1 Hazardous wastes, or wastes managed as hazardous, with a beat of combustioa greater than 6000 BTU/lb.
MPG 1, Page2of3
Company Confidential
DSw 108086
WATER_PCB-SD0000021633
USEPA has established cancer unit risk values: c) those contained on the International Agency for Research on Cancer (IARC) group 1 and 2A lists: d) other sitespecific pollutants identified by the plant that appear to warrant consideration (including those in significant quantities reportable via SARA Section 313). Plants outside the United States will use the above-given pollutant list plus any additional air pollutants on any local regulatory list that the plant manager deems important.
Each plant will maintain a list of all such air pollutants, ranked by established and approved protocols. Depending upon (he pollutant's relative ranking and if required by the protocols, the plant will use appropriate dispersion modeling techniques to determine potential maximum downwind concentrations for each such pollutant at specified receptors representative of the exposed population utilizing appropriate dispersion modeling techniques. Appropriate assessments of potential human health impacts at the community receptor points will then be analyzed according to protocols established by the company's Environmental, Safety and Health staff. Any potentially unreasonable risk to human health that is identified will be expeditiously reduced to acceptable levels through appropriate actions.
The company will conduct aquatic safety assessments to determine the measurable impacts, if any, of its effluents on receptor water quality. The assessments should include both direct and indirect discharges (if applicable) with the mitigating impacts of the publicly owned treatment works (POTW) taken into account for the indirect discharge assessments. Any potentially unacceptable impacts to the aquatic environment identified will be mitigated in a timely manner. A reconfirming assessment will be conducted to verify that the impacts have been reduced to acceptable levels.
All initial air emission and surface water release assessments required should be conducted for each of the company's worldwide manufacturing sites within two years of the EPC's approval of this guideline. Operating units will review the status of the assessments annually, and if any significant changes have occurred at a plant site, determine whether the assessment should be repeated. Any such reassessments will be completed within 12 months.
1.7 Measurement
The following indicators will be used to measure progress against this guideline:
1.7.1 Annual progress toward achievement of 90 percent SARA Section 313 air emissions reduction goal.
1.7.2 Annual progress toward achievement of 70 percent worldwide SARA Section 313 chemical releases and off-site transfer reduction goal.
1.73 Achievement of contingency planning for reduction of use of deep-well injection.
1.7.4 Annual progress toward goals involving discontinued deep-well injection of RCRA hazardous waste streams and toxic SARA Section 313 chemicals.
1.7.5 Am Emissions and Water Release
Assessments
The company's air and water steering committees will be responsible for tracking the air emission and water release environmental assessments conducted at each site and maintaining an ongoing list of the assessments' current status. In addition, ti'C plant's environmental compliance audit will check the current status of these assessments and report on progress as pan of the audit's findings.
1.8 Coordinators
Where clarification is required, the following coordinators should be contacted:
WASTE MANAGEMENT D. B. Redington, ESH, Corporate, A3NA (314) 694-6503.
ASSESSMENT C. D. Malioch, ESH. Corporate, A3NA (314) 694-8889.
(Revised and approved by the Environmental Policy Committee, February 18,1994.)
DSW 10808-7
MPG 1. Page 3 Company Confiden
WATER_PCB-SD0000021634
MOWS. A. P1ERLE Me* PrMKMnl
Monsanto
Monsanto Company 800 N. Undbergh Boulevard SL Louis. Missouri 63167 ---------- Phone:^314) 694-1000__ _
November 11, 1992
To Our Employees:
'
......
..............._
Monsanto Company is dedicated to ensuring the safety of our employees, customers, communities and the environment. This is the commitment of the Monsanto Pledge, which serves as the umbrella for our overall environmental, safety and health program.
In support of this commitment, we have developed the "Monsanto Pledge Guidelines." These new guidelines replace our Environmental, Safety and Health Guidelines. They set forth the management expectations for environmental, safety and health performance, and they describe key resuits against which progress will be measured.
The Monsanto Pledge Guidelines update our Environmental, Safety and Health Guidelines, and incorporate Responsible Care, the continuous improvement initiative created by the chemical industry worldwide.
------ Thenew-gtridcBnes have been approved y4he-Envitonm*>ntai Pniiry rninmitt^, Cpnfnrmanrp wTtfi THe'sbifirdl U16 gldgailHKl!>Tima?pduII]Oitiimipi eonBerftbIel^tua<rffidThhoVatlOTvjs:.'--rr '
.____ expeeted in tailoring the guidelines for specific operating units
Please incorporate your existing plans and programs as appropriate to meet the Pledge Guidelines and add any specific programs or requirements that reflect special needs of your business.
To fulfill the Monsanto Pledge, we must engineer change and add value to our businesses. In this way, we can build a competitive advantage to sustain our leadership position in environmental, safety and health improvements.
This Monsanto Pledge Guidelines book should be treated as "company confidential." The section entitled "Introduction," pages i - iii, contains a summary of the Pledge Guidelines and can be used in external discussions.
Sincerely,
Michael A. Pierle
DS w 107930
WATER PCB-SD0000021635
I. INTRODUCTION
TABLE OF CONTENTS
III. MONSANTO PLEDGE GUIDELINES
1. Pollution Prevention
2. Employee And Community Safety And Health
3. Process Safety And Emergency Response
----4. Product Stewardship
-
------ --
5. Chemical Distribution
................. -
........6. Groundwater And Soil Quality
. .. _
7. Outside Processors
8. Community Awareness At Manufacturing Sites
-------
.
.. ...... _..
-
Tv.--otheiTguideOnes^
~~
1. Environmental, Safety And Health Reviews Of Capital Projects
2. Environmental, Safety And Health Reviews Of Divestitures Or Acquisitions Of Property And/Or Businesses
3. Environmental, Safety And Health Protection For Investments Over Which The ...... Company Does Not Have Operating Control - ..........
----------4, P^producliv^arardsTilThf..~* * * V. VI.
-- ^ 3. Safe Haiulllng'OPCaiLhiogem
--- ---
-- ...
6. Contractor/Guest Environmental, Safety And Health
7. Use Of Animals In Research Facilities
8. Ozone-Depleting Chemicals (CFCs)
9. Environmental, Safety And Health Compliance Auditing
V. PROCEDURES
1. Employee Health And Exposure Communications 2. Transmittal To The United States Environmental Protection Agency Of Substantia]
Risk Information Under The Toxic Substances Control Act 3. Recording Allegations Of Significant Adverse Reactions Under The Toxic
Substances Control Act 4. Premanufacture Notification To The United States Environmental Protection
Agency Under The Toxic Substances Control Act 5. Occupational Fatal Accident Reporting 6. Transmittal Of Toxicology And Health-Related Data To United States Regulatory Agencies
VI. REFERENCES Appropriate Responsible Care Program Or industry Initiative
OSW 10 793J.
WATER PCB-SD0000021636
INTRODUCTION
Monsanto's Environmental, Safety and Health Program - The Monsanto Pledge
s, customers. communities and the erivlrordnent. Through the Monsanto Pledge, we have committed publicly to pursue a course of environmental stewardship - one that goes beyond what is required by the law.
I. THE MONSANTO PLEDGE
................ .........
Each of the company's environmental programs and commitments is embodied by the seven-point Monsanto
Pledge. Announced in 1990 by Monsanto's chairman. Richard J. Mahoney, the Pledge represents Monsanto's
environmental commitment to sustainable development.
.......
_ The Monsanto Pledge
It is our pledge to: reduce all toxic and hazardous releases and emissions,
working toward an ultimate goal of zero effect; ensure no Monsanto operation poses any undue risk to
our employees and our communities; work to achieve sustainable agriculture through new
keep our plants open to our communities and involve the community in plant operations; manage all corporate real estate, including plant sites, to benefit nature; and search worldwide for technology to reduce and eliminate waste from our operations, with the top priority being not making waste in the first place.
At the core of the Pledge is our belief that the public grants us the right to operate every day - and every day, we must work to earn that right. The Pledge recognizes that outstanding environmental, safety and health performance isn't a cost of doing business, but is integral to our business success. It assumes that compliance with the law and our internal guidelines is basic, wherever we do business. But the environmentalism embodied in the Pledge is far more than compliance.
The Monsanto Pledge sets the overall direction of the company's environmental, safety and health program. Specific guidelines detail our efforts to achieve the Pledge.
DSW 107932
I
WATER PCB-SD0000021637
II. MONSANTO PLEDGE GUIDELINES
------
All of Monsanto's operations worldwide observe eight Monsanto Pledge Guidelines that help ensure that our products and operations fully protea human health, safety and the environment - while meeting or exceeding existing regulations.
1. Pollution Prevention -- The company will work toward the ultimate goal of ensuring zero effect attributable .. .jo waste in all media. It will research, design and operate its facilities to minimize the generation of process and
nonprocess waste and the potential effect of chemical releases to the enviibiunenL Fdf waiste and releases'that'1 remain, the company will comply with regulations, while minimizing environmental threat and long-term liability.
2. Employee and Community Safety and Health -The company will provide a healthful and safe environment for its employees, site visitors, contractors and neighbors. It will evaluate employee health status, determine and monitor workplace factors affecting employee safety and health, and comply with both the company's workplace exposure guidelines and governmental safety and health regulations. It will review major capital projects to protea the health of its people at work and that of people in the community.
3. Process Safety and Emergency Response - The company will research, develop, design and operate processes in a manna that protects the health and safety of employees, site visitors, contractors and neighbors. Beyond compliance with appropriate governmental regulations, the company will apply such standards and programs as necessary to manage operational risks at a level that ensures its continuing right to opaate. All company sites will complement this effort with strategies to mitigate risk in the event of an incident . including site emergency response and support of comparable efforts within the community.
4. Product Stewardship - The company will research, develop, design, assess, manufacture, market and
dispose of its products so that they meet societal needs and do not pose undue risk to human health or to the
environment during all stages of their life cycles. The company will work with produa stake holdas (suppliers,
employees, distributors, customers, consumers and disposers) to understand and reduce risks associated with the
life cycle of the company's products. ..............
..
6. Groundwater and Soil Quality -- The company will design and operate facilities to protect groundwater and soil quality. The company will assess groundwater and soil quality at its facilities and pursue remedies for releases that threaten health or the environment. The company will address on-site and off-site contamination of groundwater and soil attributable to its operating and waste practices to ensure protection of health and the environment.
7. Outside Processors -- To support its operations, the company will select outside processors that will operate with concern for worker safety, regulatory compliance, community protection and protection of the environment.
8. Community Awareness at Manufaauring Sites - The company will fosta its employees' and the public's right-to-know through a commitment to openness, involvement and community dialogue. The company will be responsive to questions and concerns about human safety, health and the environment at its manufacturing sites.
Included in these guidelines are Monsanto's voluntary programs to prevent pollution and improve safety performance. Also included are specific elements of the Responsible Care initiative.
DSW 107933
1/
WATER PCB-SD0000021638
III. RESPONSIBLE CARE
Monsanto actively participates in the chemical industry's Responsible Care initiative, the most ambitious initiative on environmental, safety and health issues ever undertaken by a manufacturing industry. Responsible Care is woven into the very fabric of Monsanto's commitment to environmental, safety and health protection worldwide. It is an Important tool to help the company fulfill the Monsanto Pledge.
-^jTRcsponSble Cafe codes of management practice are included in the Monsanto Pledge Guidelines:
1. Community Awareness and Emergency Response -- to bring company operations and local communities together through communication and cooperative emergency planning.
2. Distribution -- to make the transportation of chemicals safer, regardless of the carrier or mode of shipment.
3. Pollution Prevention -- to decrease the amount of pollution and hazardous waste generated by
manufacturing operations. "
_
4. Process Safety - to prevent fires, explosions or chemical releases from manufacturing plants and processes.
5. Employee Health and Safety - to improve continuously the protection of employees, contract workers and
visitors at company sites.
'
- 6. Product Stewardship - to reduce the risks to health, safety and environment at every stage of the
company's products, from proposal to disposal.
' ''
- ~ ----
.
Responsible Care is an important part of the operation of every Monsanto facility. It is a vital part of our effort to earn the public's trust and the privilege of continued operation.
By weaving Responsible Care elements into its environmental, safety and health initiatives. Monsanto is forming - the solid foundation it needs to ensure the welfare of its employees, customers, communities and the environment.
Note: Responsible Care is a registered service mark ofthe Canadian Chemical Producers Association and the U.S. Chemical Manufacturers Association, and is an initiative that is being adopted increasingly m countries around the world.
DSH 107934
lit
WATER PCB-SD0000021639
CT/ze ^Monsanto rPledge
It is our pledge to:
<3 reduce all toxic and Hazardous releases and emissions, working toward an ultimate goal ofzero effect;
<3* ensure no lMonsanto operation poses am* undue risk to our employees and our communities;
<3fr work to achieve sustainable agriculture through new
technology and practices;
.. '
<3t ensure groundwater safety;
keep our plants open to our communities and involve the
^mmumty-n^planUjpemtionsi^____________; ' ~
&Hnawge all corporate rea Svzmrmrrrsrmnmwnriiii+vf* to benefit nature; and
<3t search worldwidefor technolog\* to reduce and eliminate waste from our operations, mth the top priority being not making it in thefirst place.
Monsanto
January 1990
WATER PCB-SD0000021640
Jtp***' .
MONSANTO PLEDGE GUIDELINE
#l
^
pollution prevention ~ J ....... - ^ T
w
The company will work toward the ultimate goal ofensuring zero effect attributable to waste in all
media. It will research, design and operate its facilities to minimize the generation ofprocess and
nonprocess waste and the potential effect ofchemical releases to the environment For waste and
releases that remain, the company will comply with regulations, while minimizing environmental
threat and long-term liability.
......
...... .........
KEY RESULTS
-----------
Reduce by 90 percent die company's 1987 level of
worldwide air emissions of chemicals named by the
United States Environmental Protection Agency _. r~.
(USEPA) under Title iff of the Superfund
' ''
Amendments and Reauthorization Act (SARA Section
313) and chemicals of local concern outside the
United Slates by the end of 1992.
Reduce by 70 percent the company's worldwide SARA Section 313, European Community Priority Pollutant List (EC 129) and carbon monoxide............
-the enA
~ r * --------
Discontinue the deep-well injection of Resource Conservation and Recovery Act (RCRA) hazardous waste streams and SARA Section 313 toxic chemicals by the end of 1999.
PROGRAM
1.1 Process Waste
The operating units will integrate into their release reduc tion plans the corporate goal of reducing all toxic and hazardous releases and emission to all media, working toward an ultimate goal of zero effect For reducing releases from processes, the order of preference is source reduction, followed by reuse, recycling or co-product sale, and finally by incineration or other treatment to reduce the volume and/or toxicity of pollutant streams.
The development and use of technologies that improve competitive positions will be emphasized.
The operating units will integrate into their releaseiedhCtion plans the following corporate goals: - - ;
Reduce by 90 percent the company's 1987 level of worldwide air emissions of SARA Section 313 chemicals and chemicals of local concern outside the United States by the end of 1992.
Reduce by 70 percent the company's worldwide ^ARA"Section 313, EC~129and carbon monoxide-- Chemical releasj'to"flnneaianaiMrOTf^flte:Transfenvj hy end nf 1005. Th> January 19110 SARA 313 and - EC 129 lists plus carbon monoxide apply through the end of the multimedia release reduction program.
An effect-based release reduction target will be established every five years beginning in 199S, working toward an ultimate goal of zero effect. By the end of 1993. a method and process for an effect-based reduction program for toxic chemicals will be developed.
1.2 Nonprocess Waste Each facility will maintain an inventory of all nonprocess sources of waste generation, including power generation, office and maintenance operations, general warehouse trash, packaging/shipping materials and similar sources.
1.3 Underground Well (Deep-well) Injection
MONSANTO COMPANY
'
0SW 107936
MPG 1. Pape 1 of 3 Company Conadentiol
WATER PCB-SD0000021641
The company will discontinue deep-well injection of RCRA hazardous waste streams by the end of 1999. It will also apply best feasible technology to virtually eliminate the deep-well injection of SARA 313 chemicals. The company's name will not appear on the list of companies making significant use of injection wells for disposal of SARA chemicals for the reporting year 2000 and beyond. The con^any^u^jtemcmstrate ------progress hu arhiMrfng in 1996m 80 percent reduction of injected SARA chemicals against the 1990 base'
hazardous, the company will take into account public expectations, emerging trends and worldwide company practice regarding the same or similar wastes.
Contractors hired for land disposal of wastes will be subject to contracting and assessment requirements (see Pledge Guideline No. 7. Outside Processors). In the United States, the use of off-site hazardous waste landfills will be approved by the Environmental Policy Committee ahd wifi be hmitedin-ntiniber-.------- ---------
reporting year.
Medical wastes generated at the company's locations
To be prepared for the possibility of mandatory -- -- regulations, the company intends to select by the end of 1995 optimal technical strategies for total withdrawal
wiB be incinerated prior to land disposal of residues. Assurance of incineration will be obtained via manifests or equivalent documents if manifests are not available.
from deep wells. This preparation will include study- _.
...........
grade estimates to achieve non-brine, treated surface
Each company location wilimaintain a record of both
discharge. All operating units will continue where . _
the on-site and the commercial waste treatment, storage
possible to challenge the technical impediments to total-------- and disposal sites it uses. ......
withdrawal from deep wells...... ' ~
. 1.6 Air Emission and Water Release Assessments
No new uses of deep weUs for hazardous or toxic materials are permitted. A "new" use of deep wells is defined as injection of streams from new products or the addition of substances not previously injected at that site. New internal or external uses of deep wells for nanhazardous wastes and nontoxic chemicals will be considered by the Environmental Policy Committee (EPC) only on an exception basis and within the "constraints of these guidelines The economics of tnv
ijiBCBMt
**rhnnln{,v r>tner tnan tne uit 01 deep
The company wiB conduct and maintain an ongoing assessment of potential human health'impacts for : selected, routinely emitted air pollutants. It will develop appropriate control strategies to reduce identified, potentially unreasonable risk of harm to human health in surrounding communities. The list of air pollutants to be studied include: a) those listed under Section 112(b) of the U.S. Clean Air Act; b) those for which the USEPAhas established cancer unit risk values; c) those
raiThf. tnifm7>r>oai Agcncy-for Rescarch.on,___
1.4 Polychlorinated Biphenyls-^TCB-Free" '
All company-owned sites (e.g., warehouses, plants, offices) located in the United States will minimize the potential for releases of polychlorinated biphenyls (PCB) by becoming "PCB-free" of Toxic Substances Control Act (TSCA)-conlaminated articles by the end of 1994.
specific pollutants Identified by Uit (Mlilii lliai jpjx. u n.i. warrant consideration (including those in significant quantities reportable via SARA Section 313). Plants outside the United States wiB use the above-given pollutant list plus any additional air poUutants on any local regulatory list that the plant manager deems important.
1.5 Land Disposal
Landfill of "acutely hazardous" wastes' and "incinerables"2 will not be practiced. For hazardous wastes and wastes managed as hazardous, fixation of particularly mobile, persistent or bioaccumulative wastes will be accomplished whenever warranted and feasible. In making the decision to manage wastes as
Each plant will maintain a list of all such air pollutants, ranked by established and approved protocols. Depending upon the pollutant's relative ranking and if required by the protocols, the plant will use appropriate dispersion modeling techniques to determine potential maximum downwind concentrations for each such pollutant at specified receptors representative of the exposed population utilizing appropriate dispersion
1 As lined in 40 CFR 261.33(e), pliu ny muuurcj containing greeter than 3 percent. 3 Hazardous wanes, or wastes managed as hazardous, with a beat of combust!oc greater than 6000 BTU/lb.
MPG 1. Pape 2 of 3 Company ConHdential
DSW 107937
WATER_PCB-SD0000021642
modeling techniques. Appropriate assessments of potential human health impacts at the community
hazardous waste streams and toxic SARA
Section 313 chemicals.
receptor points will then be analyzed according to protocols established by the company's Environmental, Safety and Health staff. Any potentially unreasonable risk to human health that is identified will be expeditiously reduced to acceptable levels through appropriate actions.
1.7.5 Air Emissions and Water Release
Assessments
The company's air and water steering committees will be responsible for tracking the air emission and water release environmental ^^ ^ .^-^assessinents conducted at each site and
The; determine the measurable impacts, if any. of its effluents on receptor water quality. The assessments should include both direct and indirect discharges (if applicable) with the mitigating impacts of the publicly owned treatment works (POTW) taken into account for
list of the
''
assessments'current status. In addition, each
plant's environmental compliance audit will
check the current status of these assessments
;--and report on progress as pan of the audit's
findings.
the indirect discharge assessments. Any potentially unacceptable impacts to the aquatic environment
.
1.8 Coordinators - . ..
.
identified will be midgated in a timely manner. A
Where clarification is required, the following
reconfirming assessment will be conducted to verify that
coordinators should be contacted:
the impacts have been reduced to acceptable levels.
WASTE MANAGEMENT
All initial air emission and surface water release assessments required should be conducted for each of '
D. B. Redington, ESH, Corporate, A3NA (314)694-6503.
the company's worldwide manufacturing sites within two years of the EPC's approval of this guideline. Operating units will review the status of the assessments annually, and if any significant changes have occurred at
ASSESSMENT C. D. Malloch, ESH, Corporate, A3NA (314) 694-8889.
a plant site, determine whether the assessment should be
repeated. Any such reassessments will be completed
within 12 months. -------------------- ------,, __________________________
..
......
._
(Revised and approved by the Environmental Policy
Thft rnllnuMlip imlimmi A mill lir uwl trt WlAflenrg -
progress against this guideline:
1.7.1 Annual progress toward achievement of 90 percent SARA Section 313 air emissions reduction goal.
1.72 Annual progress toward achievement of 70 percent worldwide SARA Section 313 chemical releases and off-site transfer reduction goal.
1.73 Achievement of contingency planning for reduction of use of deep-well injection.
1.7.4 Annual progress toward goals involving discontinued deep-well injection of RCRA
............
-
OSW 107938
MPG 1. Pape?of? Company Confidential
WATER PCB-SD0000021643
MONSANTO PLEDGE GUIDELINE
#2
EMPLOYEE AND COMMUNITY SAFETY AND HEALTH
The company will provide a healthful and safe environment for its employees, site visitors, contractors and neighbors. It will evaluate employee health status, determine and monitor workplace factors affecting employee safety and health, and comply with both the company's workplace exposure guidelines and governmentalsafety and health regulations. It will review major capital projects to protect the health ofits people at work and that ofpeople in the community.
KEY RESULTS
Approach zero adverse health effects for the company's
employees, site visitors and site contractors, including
zero occupational injury and illness.
~
Certify into the United States Occupational Safety and Health Administrative's (OSHA) Voluntary Protection Program (VPP) or equivalent at all facilities where appropriate by the end of 1997.
Reduce by SO percent the company's 1991 level of "accidental releases of hazardous materials from__
PROGRAM
2.1 Health Surveillance and Assessment
The company will monitor and evaluate the effect of work exposures on employee health by providing occupational health surveillance in all locations. The goal is to offer periodic assessments for all employees. Health surveillance and periodic health assessments will be conducted by the company or by contract health professionals in accordance with the Occupational Medicine Program as defined in the company's Occupational Medicine Program Manual.
2.2 Workplace Surveillance
The company will conduct workplace surveillance to identify potential health risks, evaluate hazards based on current toxicological and epidemiological information and initiate appropriate safeguards to protect employee health.
2J Audits and Reviews
The company will perform periodic on-site audits and reviews of worldwide operations to evaluate status of safety, occupational health and,jpdustnal hygiene pro grams. It will utilize observations and recommendations to achieve and maintain regulatory and code compliance, attain appropriate technological sophistication, reduce the probability of illnesses and injuries, and support employee safety and health education.
2.4 Regulations and Guidelines SDiaatip5riywTil-aehiev^ yrwt-maintaincompliance.
with it _
sign, safe work; injury and illness recordkeeping, workplace exposures, health surveillance, and community safety and health. If regulatory guidelines are unavailable or inadequate to protect worker health, the company will establish guidelines where appropriate.
2.5 Data Management
The company will collect and enter workplace materials, worker exposure, work history and employee health assessment data into the Monsanto Environmental Health Information Analysis & Reporting System (MARS) data base, which will be used to perform epidemiological and other appropriate studies to evaluate worker health and enhance worker protection.
MONSANTO COMPANY
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The company will establish guidelines for classifying
2.10 Security
and recording injuries and illnesses and monitor company-wide performance and adherence to federal
The company will establish security procedures and systems to control entry and exit of personnel and___
and local regulations on recordkeeping. It will issue monthly summaries of appropriate statistics and will
materials at its sites.
~
produce other publications designed to improve awareness and to communicate relevant technologies to the workplace. The company will develop ways to -understand the causation of injuries andexposuresjs - ^
2.11 Measurement
The following indicators will be used to measure progress against this guideline:
well as techruques forprevemion.-': ~^^
t
2.6Loss Prevention Reviews
a? ~ ::: Annual progress toward operating tmit'sgoa&for - ....... the Total Recordable Rate (TRR).
Annual progress toward entry of 100 percent
The company .will conduct safety and industrial hygiene ..
United States manufacturing and service locations
reviews on design, start-up and operational issues for
into VPP by end of 1997.
major new installations and expansions.
Releases as reported per the company's worldwide
2.7 Professional Activities
------- --- - system.--------- -------------- ----------------- -
The company will advance occupational health and safety consciousness through employee participation in
Systematic review of employee health and
___ industrial hygiene data.
....
trade and professional associations and other coopera
tive endeavors.
"
-^
2.12 Coordinators
.... Where clarification is required, the following ^ _
2.8 Employee Education ------------------------------------ --------- Coordinators should be contacted: -- ---^
The company will provide employee training, orientation and education in safety and health.
. V. E. Boyen, Director, Safety & Personal Protection, A2NG, (314) 694-6007
-
2.9 Contract Employees
The company will provide contract employees with any required occupational health surveillance, safety and ~
P. A. Easterday, Director, Industrial Hygiene, A3NL, (314) 694-8836
J. H. Baker, Director, Occupational Medicine.
Mn A, rnnrrnrtnr/T.nrrt, sT^rrrrTTm health and Sufety, Sites located in the United States. will meet the requirements of the contractor environmental, health and safety guideline.
(Revised and approved by the Environmental Policy Committee, October 22,1992.)
MPG 2. Pape 2 of 2
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WATER PCB-Sd600002 1645
MONSANTO PLEDGE GUIDELINE
.... .....................................
#3
PROCESS SAFETY AND EMERGENCY RESPONSE
The company will research, develop, design and operate processes in a manner that protects the health and safety ofemployees, site visitors, contractors and neighbors. Beyond compliance with appropriate governmental regulations, the company will apply such standards and programs as necessary to manage operational risks at a level that ensures its continuing right to operate. All _ company sites will complement this effort with strategies to mitigate risk in the event ofan incident, including site emergency response andsupport ofcomparable efforts within the community.
......... KEY RESULTS
Sustain no major losses from catastrophic incidents.
Retain the company's preferred risk status with'..... . insurers.
Reduce by 50 percent the company's 1991 level of accidental releases of hazardous materials from production operations by the end of 1996.
Incur no major injuries to employees or neighbors from ~ a plantprocess incident.----------- -------------- _-----------
designs. Designs should incorporate relevant consensus standards as appropriate. Additionally, the Safety and . -Property Protection (S&PP) staff shall provide supplemental guidance through Design Guides, Tecfacts . and related documents (e.g- Guidance Notes as published by S&PP, Europe/Africa).
3.3 Project Reviews
All projects (new processes, products or facilities) will undergo safety reviews to ensure adherence to applicable --;--internal and external standards as well as tCLexamine the
3.1 Process Development and Design
Every new process will be characterized in a document (e.g.. Tentative Process, Red Book Processfor Engineering Design) that describes all materials, equipment and processing conditions, including known safe limits. Design and engineering will be based on such documentation for a new process and on existing operations if there is already an established process. The basis for design of all major operating components and critical safety systems will be recorded in a design manual. Any new or expanded facility will be reviewed for its safety impact on the community.
3.2 Technical and Engineering Standards
The engineering organizations will maintain such standards as necessary to allow safe and effective
processes will undergo a research stage review.. participation from the Environmental. Health and Safety (ESH) staff is required for projects managed by an operating unit's engineering organization. All major projects should also have a pre-startup review to confirm that all recommendations from prior reviews and hazard analyses (if performed) have been addressed.
3.4 High Hazardous Materials (HHM) Program
High Hazardous Materials (HHM) are those materials, that if accidentally released would pose the greatest threat to neighbors and employees. A higher level of controls and operating standards are applied to these materials. The major elements of the HHM program include the use of Hazard and Operational Study (HAZOPs). the preparation of a guideline document for each HHM. and audits once every two years.
MONSANTO COMPANY
DSW 107941
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WATER PCB-SD0000021646
3.5Operational Safety Management
Safe process operations or a continuing basis are main tained by each site by the company's commitment to a series of fundamental practices. Included are the following:
3-5.1 Operating Procedures Written procedures are kept current for all
-------- processes. They cover necessary operating ^ ~ instructions, safe handling of materials, safe - operating limits, and responses to deviations,
unusual factors to ensure that no new hazards have been introduced and that appropriate' safety margins have been maintained.
3.5.7 Incident Investigations All significant incidents that threatened or could have threatened process integrity or the well-being of involved personnel will be investigated by a specially appointed team
....... who wiil establish causes and make recommendations to prevent recurrence.
including emergency steps.
3.5.2 Operator Training All production and maintenance operators must undergo training to acquire the necessary skills and knowledge for safe execution of their responsibilities. Operators must adequately demonstrate their competence before they assume their positions; training
3.6 Emergency Response
Effective emergency response indudes not only those actions to mitigate and control the incident within the fenceline but also includes actions that address the potential impact on the community. Consequently, a site emergency response program should include the following elements; ........
must be periodically reinforced.
3.6.1 Emergency Procedures
3.5.3 Contractor Safety The company will provide contract employees with any required occupational health surveil lance, and safety and industrial hygiene indoc trination in accordance with Other Guideline No. 6. Contractor/Guest Environmental, Health and Safety Guideline. Sites will meet
Written emergency procedures will be available and kept current for each process, as _ well as for the total site. They will cover actions at each stage of the emergency including shutdown and evacuation. All employees must be trained in these procedures.
the requirements of the contractor environmental, health and safety guideline.
--
Emergency Drills: Site managers will test and audit their
-3.5.4 MaMGEHEKTOiCsaNGE.___ ~ -------- injtqnipmMit
--------; ------------------ -emergency plan annually and revise it as --^^hecessary- At intervals determined by'the -V. ~
"fi 1 n 11I1111 I linn | mi 11 11 ml alint ii recognized as the safe operating regime shall be governed by a "management-of-change"
suCthe emergeucyririUvrifl include the -- _ " active involvement uf cuummmlj ftmuujes
associated with emergency management
protocol to ensure proper safety review,
authorization, training and implementation. This protocol also will apply to capital projects on all changes made subsequent to the previous safety review. A separate protocol will apply to changes in the line organization.
3.6.2 Community Preparedness The site managers will review with appropriate community officials the nature and extent of potential inddents from the site and provide the community with assistance in
3.5.5 Critical System Inspections
emergency planning if requested.
A program involving inspection, replacement and/or testing of critical equipment or safety
3.7 Measurements
systems must be maintained in order to ensure reliable operations and system integrity.
The following indicators will be used to measure progress against this guideline:
3.5.6 In-Depth Process Audits At intervals not to exceed three years, all operations shall undergo intensive audits to examine areas of change, non-routine occurrences, new information and other
Annual progress reports on S&PP Compliance Audits, the HHM Report of the Monsanto Manu facturing Council (MMC) once every two years and site In-Depth Process Safety Audit Reports.
MPG 3. Pape 2 of 3
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WATER_PCB-SD0b00021647
Annual cost of property and business interruption insurance.
Monthly reports on SARA Title III, Section 304, reportable releases against goals.
S&PP quarterly property-loss reports.
3.8 Coordinator' ~7 ' . T .7._ _ - -
Where clarification is required, the following coordinator should be contacted:
~
V. E. Boyen, Director, Safety & Personal Protection, A2NG, (314) 694-6007
3.9 Definitions ESH: Environment, Safety and Health. HAlZOP'. Hazard and Operability Study, a hazard identification technique. HHM: Highly hazardous material (a Monsanto designation for substances posing an acute risk). MMC: Manufacturing Management Council. SARA: Superfund Amendments and Reauibdrtzauon ~ Act.
(Revised and approved by the Environmental Policy Committee, October 22,1992.)
OSy lO?9<,3 MPG 3. Pace .'Of t Company Confidential
WATER PCB-SD0000021648
MONSANTO PLEDGE GUIDELINE
................................
.
#4
PRODUCT STEWARDSHIP
The company will research, develop, design, assess, manufacture, market and dispose ofits products so that they meet societal needs and do not pose undue risk to human health or to the environment during allstages oftheir life cycles. The company will work with product stake holders (suppliers, employees, distributors, customers, consumers arutdisposers) to understand and reduce risks associated with the life cycle ofthe company's products.
KEY RESULTS
Practice the principles and key elements of Product Stewardship, as specified in appropriate programs around the world, at all the company's global ' operations.
Provide appropriate safety and handling information, including Material Safety Data Sheets (MSDSs)1. to potentially exposed employees, including contract employees and product receivers.
Worictoward-the goal of no undue risk through___________
ryrl
____
_____
Gain a competitive advantage by applying product stewardship principles that add value to the company's product offerings.
PROGRAM
4.1 Environmental, Safety and Health Information and Risk Characterization
4.1.1 New chemical products, new isolated process intermediates, and significant new uses for existing chemical products will be accompanied by adequate environmental, safety and health exposure information to support a preliminary product-risk characterization (ER-200 or EC-201, and an RAD MSDS) at the earliest practical stage of
RAD and prior to off-site shipment. A product-risk characterization (including an EC-202 or equivalent, a final MSDS and a ........shipping classification) will be completed before new product commercialization.........
4.1.2 The company's process for generating and maintaining an MSDS is comprehensive and, when coupled with human experience and professional judgment, will fulfill the requirement for a product-risk
____ characterization. Whenever significant new :_:~; r.tiafQnPation becomes available, it wilTbe ~' - revicwed asptrt-onhfJdSDS program.ta . _
satisiy regulatory Hid produtit-i Uk characterization requirements. An MSDS review/product-risk characterization will be periodically performed commensurate with product risk, with revisions performed at a minimum, every five years.
4.1.3 Product files or information systems will be maintained for all products or product families. The product files or information systems will contain the data necessary to fulfill regulatory requirements and perform product-risk characterizations and assessments as appropriate, including:
* Material Safety Data Sheets;
References to relevant literature or internal reports dealing with health and
1Materiel Safety Data Sheets (MSDSs) and Safety Data Sheets (SDSs) are interchangeable terms, and refer to the similar requirements in different countries.
MONSANTO COMPANY
OS M 10 79.V<*
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WATER PCB-SD0000021649
safety (toxicology, epidemiology, indus trial hygiene, flammability, reactivity, etc.), relevant information on composition, physical properties, raw materials, manufacturing processes, principal by products. protective measures, exposure
43 Pollution prevention principles (Pledge Guideline No. 1. Pollution Prevention) will be included as review criteria in technology-risk reviews for new and existing chemicals, and will be incorporated into the EC-2011202 (or equivalent) assessments.
information, energy requirements, wastes and disposal practices; .
4.4 Employee Education and Product Use Feedback
------ . information on use, including handling,
_ _____ 4.4.1 Employee education in the safe handling and
transport, packaging and storage, which will
use of chemicals is addressed in Pledge
either be estimated (typically for new
Guideline No. 2, Employee And Community
products), or obtained by visits or reviews
Safety And Health.. Employees with
of customer, distributor and consumer
significant customer interaction will be
practices;
A critical review of health aqd environmental effects and exposure
--
trained to recognize and feed back information about product use and misuse to the company's environmental network.
information, such as EC-201, EC-202,
4.4.2 Feedback systems to listen to stake holders,
Monsanto Work-Place Permissible
including commercial and technical service
Exposure Guideline (MWPEG) Reviews,
liaisons with customers, product hotlines,
Health Effect Reviews and Toxicology
poison control center relationships, etc., will
Reviews;
be nurtured and expanded as appropriate.
Technology Risk Reviews; ...... ............ ;
Health concerns of customers, employees or the public.
4.2 Risk Management System
4.2.1 A systematic approach to risk management
will be implemented and maintained for new
" ~ 'I~ product^Bdsting-products will be managed
^ona^ase-by-casebasis.
"
....... a i/l ttlBlr mnnapriupiii rqeinnt where needed. --
will be an integral part of the follow-up to each phase of a product-risk characterization (as detailed in Section 4.1).
4.2.3 All products will be appropriately labeled for hazard or risk, and will conform at a minimum to governmental requirements and appropriate consensus standards (e.g., ANSI, ISO. etc.).
4.2.4 Document risk-management actions will be recorded in product flies (examples of specific risk-management actions are detailed in Sections 4.3 through 4.7).
43 Product and Process Design and Improvement
4.3.1 R&D materials used in the laboratory will be handled under Prudent Laboratory Practices or equivalent guidelines.
4.5 Contract Manufacturers See Pledge Guideline No. 7, Outside Processors.
In addition, the company will provide guidance and information to contractor personnel on the safe handling and transportation of company products.
. 4.6 Suppliers............................... ... ... .......
4.6.T Up-to-date and higb-qualityproduct - --- --
---.-~iflformauotU4nciuding. as appropriate".
2
composition data and MSDSs, will be
obtained from suppliers for all raw materials.
4.6.2 Suppliers will be actively engaged as appro priate, commensurate with raw-material risks.
4.7 Distributors, Customers and Other Direct Product Receivers
4.7.1 The company will ensure that MSDSs and other appropriate safety documents are provided to all direct product receivers.
4.7.2 As appropriate, the company will actively involve product receivers in dialogue and outreach regarding appropriate risk characterization, risk management and risk reduction. Where applicable, the company will assist in conducting audits. If improper rvt'nvolving company products are
MPG 4. Pace 2 of 3 Company Confidential
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WATER_PCB-SD0000021650
identified, the company will work with the ` product receiver to improve the practices. If
adequate improvement is not evident, the company will take appropriate action, including termination of sale if necessary.
4.7.3 The company will actively seek productreceiver involvement in the continuous improvement of company products and as a . means of differentiating those products in the marketplace on the basis of environmental, safety and health stewardship.
4.8 Responsibilities
4.8.1 Product stewardship is the responsibility of the . business units. Each operating company, free
standing division or world area will assign certain employees the responsibility for ensuring that this program guideline is met.
4.8.2 Guideline oversight is the responsibility of the corporate Environmental, Safety and Health staff.
4.8.3 The corporate staff and business units are jointly responsible for developing information needed for product evaluations. This includes periodic re-evaluation of new information relevant to the product on a regular basis.
4.9 Measurement rThrfoIlowing indicators will be used to measure "pregfgsragalmt thls^gnideiipe:
4.9.1 Progress in meeting internal and external requirements for all new product introductions (i.e., EC 201/202 approvals and governmental approvals).
4.9.2 Progress in determining product hazards.
4.9 J The growth of knowledge about bow company products are used and the resultant exposures to people and the environment.
4.9.4 The availability of adequate environmental, safety and health data to the ultimate product receiver.
4.9.5 Increased understanding and diminution of the risks and environmental impacts associated with a product throughout its life cycle.
4.9.6 Differentiation of company products in the
' marketplace.'
~ ' :
4.10 Definitions
Product Receiver: An entity (not an individual) to whom the company transfers product. This definition includes product receivers such as brokers or transporters who may not fairinto the traditional customer category.
..... Product: Chemical substances and mixtures.
materials and equipment, articles, licensed
technology and services related to product use that
are sold, distributed in commerce, or otherwise
/. provided.
_-
4.11 Coordinator
Where clarification is required, the following coordinator should be contacted: .
J. R. Condray, ESH, Corporate, A3NA (314)694-8883. ........................................
DSW 107946
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WATER PCB-SD0000021651
._______
_______________ _
MONSANTO PLEDGE GUIDELINE
#5
CHEMICAL DISTRIBUTION
The company will reduce potential risk to its employees, the public, carriers, distributors, contractors, customers1 employees, and the environment in the distribution ofchemicals.
KEY RESULTS
Work toward incident-free performance in the distribution of chemicals, including taw materials, intermediates, finished products, byproducts and wastes.
PROGRAM
..
5.1 Chemical Distribution Incident Reduction
5.1.1 The company will continue to improve chemical distribution in order to effect incident-free performance. An "incident" is defined as any undesirable event occurring during a chemical
~...distribution process over which the company has.........._ dir^controIWlugueace~aatTe3ultjiraniiqury,A^--?-^-
- relanrt of a cbem^i ^/<xjiamageJ8Lproperty or* the environment
5.1.1.1 The company will improve the carrier selection process so as to identify and contract transportation services with those carriers who consistently demonstrate safe performance in the movement of the company's chemical products.
5.1.1.2 The safety of chemical transportation practices will be continually improved through application of Total Quality/Total Partnership concepts and tools to achieve the company's goal of incident-free performance.
5.1.1.3 The company will continue to support The Agricultural Group's Bulk No-Spill Delivery Program.
5.1.1.4 Hie company will develop and apply technological advancements to improve
. chemical distribution safety and will share these with the industry as appropriate.
5.1.1.5 Through its emergency response system, the
company will provide technical advice and
~ assistance in a responsible and timely
manner for "outside plant gate" incidents
involving its chemical products. The company
will measure and continuously improve its
response capabilities. Trained personnel will
be physically present, in an expeditious
manner, at the emergency site upon request
. of the local emergency responder or public
^official, orwbcn the company feels a ..
'
qualified emergencyvam ran irssen iheT T T
" severity of an incident or eflM ffCBBmnF=r-
nity's concerns about the company's
products.
Program Emphasis Areas
5.1.2.1 Each shipping location will have a current plan for responding to chemical transportation emergencies involving products/materials within its scope. The plants* emergency responders will receive regular training that meets or exceeds regulatory or industry standards.
5.122 Training history for all emergency response personnel will be documented.
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S.UJ The company will discuss with emergency responders and tbe public tbeir concerns about chemical distribution. Tbe company will encourage partnerships with local communities and local emergency responders along chemical transportation routes, as well as in those communities where its chemical plants are located.
5.1.2.4 Tbe total emergency response plan will be continuously monitored and improved. Detailed post-incident repons and preventive action plans will be provided as training aids to all emergency responders. -
.
5.1.2.5 Distribution accidents/incidents and any resulting loss of containment will be reduced according to a documented distribution riskmanagement methodology. An initial qualitative risk-assessment methodology will be made available for use. Quantitative risk assessment models will be evaluated for especially sensitive materials.
5.1.2.6 Regulatory changes that affect the
distribution of the company's products will
be monitored and changes will be
.
communicated to shipping locations.
Compliance audits and training will be
conducted at all company shipping locations
as appropriate and reported on annually.
5.1.2.7 The company will support community . . , : outreach urograms bv offering plant
emergency-respuudm in cuuunuiuues-------neighboring tbe company's distribution network.
5.1.2.8 Tbe company will, as appropriate, through routine communications with the public, emphasize continuous improvement in safe chemical distribution and will be responsive to public concerns.
5.1.2.9 As appropriate, trained plant employees will be the company's "ambassadors" to tbe community to convey the company's progress and its commitment to improving the safety of chemical distribution and effectiveness of its emergency preparedness and response.
5.1.2.10 Tbe company will recognize, as appropriate, the potential for adding value to its products.
52 Chemical Distribution Safety for Warehouses and Terminals
5.2.1 A seamless policy of operating safety results will be extended to warehouses and terminals that receive tbe company's products. This policy will incorporate standards comparable to tbe company's.
5.2.1.1 Tbe company will use precontracting guidelines in tbe selection process to assess firms that can handle company products in a manner that is safe for its employees, the public and the environment
5.2.1.2 Tbe company will provide information on its policies, procedures and requirements on the safe handling and transportation of chemicals to warehouse and terminal personnel.
5.2.1.3 Tbe company will apply Total Quality .... Management concepts and tools to all
aspects of contract management for continuous improvement in safety and reliability of provided services.
5.2.1.4 The company will use agreed-upon performance measurements and periodic
. reviews as indicators of progress toward zero-incident status.
5.2.1.5 The company will extend its recognition of public concerns about emergency preparedness and safe distribution practices
"___ ^to aUjits distribution locations.
SH PaocitAMJlMfflAsis Areas .
5.2.2.1 Documented selection criteria that include appropriate safety measures for each product will be maintained.
S3.J1J2 Tbe company will maintain defined flows of information concerning its policies, guidelines and requirements on the safe handling of its products.
SJ.J.3 The company will conduct reviews of performance against its requirements on a specified review cycle.
5.2.2.4 Tbe company will support risk management activities and emergency preparedness at all of its distribution locations.
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5J Measurement
Appropriate measurement systems will ensure continuous improvement toward stated goals and objectives.
5.4 Coordinator
Where clarification is required, the following coordinator
should be contacted:
........................
--------
n ^ -Williams, Chemical. Purchasing/Distribution,-------------------------------------------
BRSS.F2EA, (314) 694-8644.
t
(Revised and approved by the Environmental Policy
Committee. October 22,1992.)
.-
..
OSW i0?9<9
MPG 5. l'ape3or? Company Confidential
WATER PCB-SD0000021654
MONSANTO PLEDGE GUIDELINE
#6
GROUNDWATER AND SOIL QUALITY
The company will design and operate facilities to protect groundwater andsoil quality. The company will assess groundwater and soil quality at its facilities andpursue remedies for releases that threaten health or the environment. The company will address on-site and off-site contamination ofground water and soil attributable to its operating and waste practices to ensure protection ofhealth and the environment.
KEY RESULTS
Establish an active groundwater assessment program
at the company's facilities.
........... _
Ensure that there are no adverse public health impacts attributable to the company's wastes.
Minimize the financial impact of remedial action and third-party liability attendant to waste sites.
PROGRAM
quality will be organized at all major locations, and at lesser sites that have known groundwater issues. Follow-up plans will address priority concerns. The assessment status and plans will be updated in a summary report during the second quarter of each year.
Any newly purchased, existing operation will be subjected to the seven-point protocol for assessment of possible groundwater contamination. The coordinator of this guideline (see 6.6 herein) will supply a copy of the assessment protocol upon request
6.2 Protection
6.2.1 Groundwater Protection Plans
Each location will maintain a groundwater protection plan that includes inspection, testing and maintenance of facilities that
-------- could contaminate groundwater (e.g.. sewers, process lines, sumps, tanks, loading/unload ing areas). The groundwater protection plans and designs will be commensurable with the risk posed by the specific situations.
6.2.2 FActunr Design
New, replacement or expansion facility designs (including sewers and lines) will consider such options as aboveground and/or double containment, improved materials of construction, and/or cathodic protection to provide improved assurance against ^3*P^^|6wj!nuiimination. - -
New, replacementor expanded surface----impoundments for wastewater treatment or storage must be approved by the Environmental Policy Committee on an exception basis.
New storage tanks for materials that could cause contamination will be provided with impervious secondary containment (e.g., dikes, liners, vaults, double wall) unless a clear showing is made on a tank-by-tank basis during project reviews that vessel contents (e.g., dilute wastewaters) or setting (e.g.. in battery containment, other adequate containment systems) do not warrant such containment Existing storage tanks will be reviewed in normal environmental audits.
MONSANTO COMPANY
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6J Abandoned Waste or Groundwater Contamination
When on-site abandoned waste or groundwater contamination is discovered, appropriate assessment of impacts on human health and the environment will be earned out. Corrective action will be taken, as necessary, in a planned, orderly process to remediate soil and groundwater impacts that threaten-human health and the environment.
6.4 Superfund
'
~
The company will act to ensure that there are no public health impacts attributable to its wastes at "Superfund" sites.
6.5 Measurement The following indicators will be used to measure progress against this guideline:
6.5.1 Submission of annual groundwater assessment summary reports by each plant subject to reporting.
6.6 Coordinator Where clarification is required, the following coordinator should be contacted:
D. B. Redington, ESH, Corporate. A3NA, (314)694-6503.
When the company becomes aware of involvement in "Superfund" sites, it will actively participate in potentially responsible parties' efforts to achieve settlement The company will seek a leadership role, - when appropriate, to facilitate resolution. The operating units will cooperate to establish responsibility for sites where several units contributed wastes, and will undertake an oversight role for sites funded at the corporate level when no current operating unit has responsibility. A goal of the company is to resolve as soon as reasonably possible its share of liability and remedial plans for sites where it has a responsibility, while securing timely and cost-effective resolution.
(Revised and approved by the Environmental Policy Committee. October 22,1992.)
The company intends a lessened legalistic approach to
site cleanup negotiations. Where company
., '
_.
responsibilityisiairly fxiihlishrd.the corripany will nol"
rtelay cteanup unneressariiyby iegal. yet negatively nr----.*
perceived litigious steps. The company will pursue fair
legislation and regulations on the general issues in the
public arena, but minimizing legal risk will not be the
determining factor in the site-specific decisions.
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MONSANTO PLEDGE GUIDELINE
#7
OUTSIDE PROCESSORS
To support its operations, the company will select outside processors that will operate with concern for worker safety, regulatory compliance, community protection and protection ofthe environment.
KEY RESULTS
Manage tbe company's exposure to present and future liabilities associated with the use of outside ......... processors by maintaining current assessments and written contracts for each outside processor used.
PROGRAM
7.1 Outside Processor Selection Tbe company will use only outside processors that have been selected and periodically assessed to ensure the following:
a. their ability to protect tbe public, employees and the . . environmem adeguately from any adverse effect of - - - tbe company's chemicals, products or wastes; * " "
b. their compliance with ail applicable laws and regulations;
c. their knowledge of potential hazards and any applicable manufacturing requirements associated with the handling of company materials; and
d. their use of waste disposal methods and locations as specified in contracts, with recordkeeping of all material use and waste disposal.
Before they are used by the company, outside processors will be subject to contracts and on-site assessments and approval by the appropriate operating unit or subsidiary director of environmental operations and its manufacturing director or world area designee. Periodic reassessments will be conducted for continuing use.
Procedures will be maintained4&define4he types of outside processors subject to this program, the assessment protocols and frequency, the conditions for waiver of one or more of tbe above requirements, and other standards.
For toll manufacturing, bulk terminals and transloading, the outside processors will take title to, adopt and own the wastes and manage them as their own under manifests and contracts. For other outside processor categories (waste management, cleaning services, etc.), a processor's waste management practices will be reviewed as part of tbe on-site assessments.
Outside processors used by all operating units. subsidiaries wnrki-arM.c udUbejectax^d in one or_____ more data, bases to avoid redundant assessments and .. -- . contracts and to facilitate use of approvedprocessors. -
The above elements will be implemented worldwide, but with modifications to reflect local limitations, restraints to compliance with this program, and the extent of the company's operating control. Status and direction of the local program will be reviewed in planned environmental audits of tbe company's facilities outside the United Slates.
7.2 Measurement
'
Each operating unit, subsidiary and world area will maintain records that document the number of outside processors used, tbe number of outside processors for which assessments are current, and the number of outside processors with contracts in place.
MONSANTO COMPANY
OSW 107952
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WATER PCB-SD0000021657
7J Coordinator Where clarification is required, the following coordinator should be contacted:
D. B. Redington, ESH, Corporate, A3NA, (314) 694-6503.
(Revised and approved by the Environmental Policy Committee. October 22,1992.) 1
MPG 7. Pact . of 2
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-OSW 107953
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MONSANTO PLEDGE GUIDELINE
#8
COMMUNITY AWARENESS AT MANUFACTURING SITES
The company will foster its employees'and the public's right-to-know through a commitment to openness, involvement and community dialogue. The company will be responsive to questions and concerns about human safety, health and the environment at its manufacturing sites.
KEY RESULTS
Establish active community advisory panels, as appropriate, at manufacturing sites.
PROGRAM
8.1 Community Involvement and Dialogue
Each manufacturing site will implement a policy of openness that provides convenient ways for interested individuals to become familiar with the facility, its operations, its products and its efforts to protect human safety, health and the environment Community advisory panels, open bouses, plant tours, environmental 'awareneSTdjssl community in plant operations may be used.
Community outreach programs will be implemented at each manufacturing plant to inform key audiences (emergency responders, government officials, the media, employees, other businesses and the community) about the facility's emergency response program, chemical inventory, impact evaluation, and potential risks to the community associated with the facility. The information provided will include details on such topics as waste minimization, emissions reduction, health effects of chemicals, and efforts to ensure safe transport of chemicals.
Further, all information will include planned improvements in each of these critical areas as well as expansion activity and other projects of general interest to the community.
An ongoing dialogue with employees and members of the community will be used to assess and respond to their questions and concerns about environmental, safety and health Issues, and to involve them in the community outreach effort Each manufacturing site will conduct an ongoing assessment of employee and community questions and concerns about the site. The effectiveness of the ongoing community communications effort will be evaluated regularly by the site.
Communications training will be provided for key site and company personnel who communicate with employees and the public concerning human safety, health and the environment
'8.2 Information on Chemical Releases/Incidents
Each operating location will make available timely ~~ ~ information about routine or accidental releases of toxic chemicals and other chemicals of local concern. Appropriate audiences may include neighbors in the community, employees and the news media. Informa tion will also include progress in achieving the company's stated emissions reduction and pollution prevention goals and future plans. When possible, the information on chemical releases should be at a personal, face-to-face level, and should emphasize listening to others and discussing their concerns and ideas.
The company will publish and distribute annually an Environmental Annual Review that articulates the company's environmental, safety and health policies and its progress toward achieving stated environmental, safety and health goals.
MONSANTO COMPANY
DSM 10795*t
MPG 6. Pape lot:
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WATER PCB-SD0000021659
S3 Measurement
The following indicators will be used to measure progress against this guideline:
8.4 Coordinator
Where clarification is required, the following coordinator should be contacted:
Annual progress toward establishing community advisory panels, as appropriate, at each manufacturing site.
G. F. Barton, Corporate Communications. A2SP (314) 694-7233.
Annual dissemination of data on toxic chemicals and other chemicals of local concern at each manufacturing site, as appropriate.
Annual report of the company's status against stated environmental, safety and health goals through wide distribution of the Environmental Annual Review.
(Revised and approved by the Environmental Policy Committee, October 22.1992.)
Progress, as appropriate, toward developing routine and convenient ways for interested parties
____ to become familiar with the company's manufacturing sites, its operations, its products,---- and its efforts to protect human safety and health and the environment
Ml'G fc. Pace: of: Company Confidential
05W
107955
WATER_PCB-SD0000021660
OTHER GUIDELINE
#1
ENVIRONMENTAL, SAFETY AND HEALTH REVIEWS OF CAPITAL PROJECTS
The company's capital projects will meet the Monsanto Pledge Guidelines and will be in compliance with existing and anticipated governmental regulatory requirements. The company will review at all levels capital projects for environmental, safety and health impact before, and as a condition of, project funding.
The vice president of Environmental, Safety and Health or his designee will review those projects requiring approval by the chief operating officer, the chief executive officer or the board of directors. A formal premise review will be held for such projects or other projects with major technology changes as determined by the operating unit, technology and engineering directors. A system for reviewing other projects will be administered by the directors, environmental operations, of the operating units.
Any exceptions to this guideline must be approved by the Environmental Policy Committee.
(Revised and approved by the Environmental Policy Committee. October 22,1992.)
------- Emptoyees^assigned d evaluate a new locatiPQjpr^.^
_.
,~77 ,'3^efaQon wiIl prepare an internal environmental impact ---- - - -------
assessment addressing potential environmental....
limitations at the site as a result of the existing
socioeconomic and biophysical conditions. The effects
of the public climate of opinion and of existing and
future governmental, environmental regulations that
may apply also are to be considered.
MONSANTO COMPANY
107956
OG 1. Pape 1 of 1 Company Confidential
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OTHER GUIDELINE
. #2
ENVIRONMENTAL, SAFETY AND HEALTH REVIEWS OF DIVESTITURES OR ACQUISITIONS OF PROPERTY AND/OR BUSINESSES
Negotiations for acquisition or divestiture of property or business units and the securing of final corporate approval are the primary responsibilities of the involved operating uniL However, corporate staff review of ' environmental, safety and health factors and any attendant liability issues is required during the course of such transactions. This review should be arranged through the office of the operating unit's director of environmental operations, who will, in turn, involve appropriate Environment, Safety and Health staff and Environmental Law personnel and arrange for review by the vice president of Environmental, Safety and Health, and/or the executive vice president of Environmental, Safety. Health and Manufacturing. The review should be completed prior to seeking board of directors approval ofthe acquisition orltfivestiturer
(Revised and approved by the Environmental Policy Committee, October 22.1992.)
MONSANTO COMPANY
DSW 107957
OG 2. Pape 1 of 1 Companu Confidential
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$ OTHER GUIDELINE
ENVIRONMENTAL, SAFETY AND HEALTH PROTECTION FOR INVESTMENTS OVER WHICH THE COMPANY DOES NOT HAVE OPERATING CONTROL
The Monsanto Pledge Guidelines apply at all sites worldwide where the company has operating control. For those investments over which the company does not have operating control, at a minimum. compliance with applicable local laws, regulations and practices will be required.
If such applicable rules and practices do not provide environmental, safety and health protection that would be acceptable for company-controlled sites, the company will initiate action to bring about the necessary upgrading.
#3
(Revised and approved by the Environmental Policy------- - - ----------
Committee, October22,1992.)
"' "
MONSANTO COMPANY
DSW 107958
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WATER PCB-SD0000021663
OTHER GUIDELINE
#4
REPRODUCTIVE HAZARDS IN THE WORKPLACE
The company will use all appropriate information to ensure avoidance ofreproductive effects in workers ofboth sexes and in offspring ofworkers,
Through the departments of Medical and Health Sciences and Safety and Environmental Health, the company will do the following:
The company will conduct appropriate toxicological tests of its raw materials, products, intermediates and byproducts.
The company will review current literature for information on the hazards of chemicals and physical agents that the company uses or produces.
The company will assess safety arid health implications and the potential reproductive ----- hazards posed by these chemicals and physical agents.
The company will minimize exposure to potentially harmful materials or activities by substitution with less risky chemicals or processe when feasible, through the use of engineering, work practices, and reliable protective equipment
The company will provide the most accurate information currently available on materials or work practices thought to have reproductive health effects. - ...... ....
The company will offer counseling by qualified health professionals to employees about workplace reproductive concerns.
(Revised and approved by the Environmental Policy Committee, October 22.1992.)
MONSANTO COMPANY
OSW 1.07959
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J&&
OTHER GUIDELINE
#5
, SAFE HANDLING OF CARCINOGENS
The company will provide safe and healthful working conditions for its employees. It will comply with all governmental regulations concerning exposure to carcinogens.
The company will do the following to-ensure the safe handling of carcinogens:
If any data suggest that a chemical to which its employees are exposed is a carcinogen, and such chemical is not subject to governmental regulations, the company will evaluate those data and then take appropriate action.
If the data establish the chemical as a human . carcinogen, the company will take appropriate action to reduce exposure to the lowest reasonable level, unless exposure is already at such a level.
If the data establish the chemical as an experimental or suspect carcinogen, the company will (individually or with others) initiate a study to confirm or disprove such designation. During each study, exposure will be reduced to and/or minimized at the lowest reasonable level.
If it is concluded that a material cannot be produced or used without jeopardizing employee health, its manufacture or use will be discontinued.
(Revised and approved by the Environmental Policy Committee, October 22,1992.)
MONSANTO COMPANY
OS* 107960
OG 5. Pape 1 of 1 Compani'Confidential
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OTHER GUIDELINE
#6
CONTRACTOR/GUEST ENVIRONMENTAL, SAFETY AND HEALTH
Continuous improvement in contractor/guest environmental, safety and health performance is necessary to create an injury-free and incident-free environment at all company sites for employees and their guests.
6.1 Scope This guideline sets forth environmental, safety and occu pational health (ESH) guidelines applicable to contractors and guests who perform services on or visit company properly. All services administered by individual sites or by company engineering groups are covered. Deviations from the contractor/guest ESH process and requirements will be thoroughly documented and . approved by the location manager or as described in the Contractor/Guest ESH Guideline Manual. No deviation from regulatory requirements will be permitted.
This guideline applies initially to all company locations in the Uiuted States. Ite intent is to work toward worldwide implementation . ~
6.2 Definitions
Contractor. Any non-company person performing physical work at a site under a company purchase order or contract.
Guest: Any person visiting, performing work or providing a service at a company-managed site, including company employees who are not permanently assigned to that location.
Certified Monsanto Representatives: Employees designated by the location management to administer the Comracior/Guest ESH Guideline.
Master Monsanto Representative: The location administrator/facilitator responsible for ensuring effective implementation of the Contractor/Guest ESH process at the location, including training and certifica tion for other Certified Monsanto Representatives.
Contract: The document that contains terms and conditions of the agreement between company and the contractor and which serves as proof of their respective obligations. Contracts are to be signed by authorized representatives of the contractor and company, in a form previously approved by the Purchasing and Law departments.
6.3 Objective
_
The process described in this guideline was developed to
define requirements for all company locations to ensure
continuous improvement toward incident-free and
injury-free performance for employees and all
"contractors and guests.' ' ' '' "
-----
Through this process, it is intended that all services per formed by comtractors on company sites will be covered by written cottracts. Furthermore, the contractor is to be made aware of the requirements of this guideline before bidding, and the appropriate requirements are to be incorporated into the written contract
In accordance with the objective of providing for employee and guest safety in the execution of contract work, the company will utilize contractors who have demonstrated a high degree of compliance with workplace laws/standards, policies and practices; have a history of good health and safety performance; maintain adequate insurance coverage; and, if involved in safety sensitive work, have a substance-abuse treatment program reasonably equivalent to that of the company.
MONSANTO COMPANY
DSW 10 7961
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This process is designed to help ensure that the company will go beyond current regulations, take as industry leadership position in contractor/guest safety and ensure continuous improvement toward incident-free and injury-free performance.
6.4 Responsibilities
.
The location manager is responsible for ensuring implementation of this guideline. Each site will have a. minimum of one company master-certified representative with responsibility for administering and facilitating the Contractor/Guest ESH Guidelines.
6.5 Supporting Documentation
This guideline is supported by Contractor/Guest ESH Guideline Manual that incorporates the following requirements:
Contractor Management Systems
7
Working in an Operating Facility
Housekeeping Fire Protection and Prevention Hazardous Work Permits Occupational Health/Workplace Exposure
Monitoring
Vehicle Safety Waste Management ......
Occupational Medicine . _
Management of Change
6.6 Practices and Procedures
6.6.1 The company's contractor/guest environmental, safety and health process defines a fully integrated approach to the management of all contractors and guests within company facilities. The process is not intended to restrict management prerogatives, but rather to provide the consistency to help ensure that the Monsanto Pledge is fulfilled and the highest organizational priority is placed on the health and safety of company employees, guests and the communities in which the company operates.
OG 6. Pape 2 of A
Company Confidential
6.6.2 Contractor/Guest Environmental, Health and Safety Process (see Appendix 6.1)
Contractor Representative Training and Certification -- provides for the identification and consistent training of all individuals with responsibilities for selection and management of contractors and guests working at and visiting within company facilities.
Guest and Delivery Site Visit Process provides a consistent approach to the orientation and control of all guests, visitors and delivery people who enter company facilities, even those not under contract.
Pre-Qualification Process -- provides a consistent approach to identifying and selecting contractors, vendors and service providers who practice effective safety programs with demonstrated leadership and performance in their industry.
Selection and Approval Process -- provides a framework for the contracting of services, which includes the identification of all ESH requirements based on the task and the pre identified risk. The process stresses clear communication of the company's performance expectations before the contract is finalized.
Pre-Job Activities and Compliance Review Process -- defines a systematic approach for verifying that the contractor and all of the contractor's employees meet the contractual requirements, including orientation, training, medical testing and substance-abuse screening. Plant, operating unit and job-specific expectations are emphasized.
Work-in-Progress Process -- provides a process for the management and audit of the contractor's activities to the ongoing compliance with the company's policies, procedures and requirements. The process focuses on the cooperation between the company's certified representative and the contractor's management to achieve success ful and injury-free completion of work.
DSW 10796
WATER PCB-SD0000021667
Performance Evaluation Process ~ provides a defined process for tbe evaluation of and feedback on a contractor's performance, whether tbe contracted work is for a defined task or ongoing services. Performance evaluations are fed into tbe contractor pre qualification process and after evaluation contractors either remain on tbe pre qualification list or are stricken from it......
6.7 Contractor/Guest Responsibilities
6.7.1 The contractor/guest is responsible for compliance with this guideline as incorporated into tbe contract or otherwise communicated to die contractor in order to ensure safe
__ operations. Contractors will have a competent, well-trained supervisor in charge at tbe site at all times when its employees or those of its subcontractors
... are present. The company will not undertake direct supervision of contractor employees. However, when a . contractor employee has no on-site supervision, tbe contractor should work
- with the company's certified representative to provide for appropriate implementation of this guideline.
6.7.2 Visitors and all delivery personnel entering the location are to be made knowledgeable of site rules and regulations.
6.7.3 All contractors and guests must communicate
in English at a level of proficiency that
ensures their safety and the safety of others.
Exceptions to the English communication
requirement may be granted only by the
.....location manager.----- -
-
(Revised and approved by the Environmental Policy Committee, October 22,1992.)
~ .......... .....
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MONSANTO CONTRACTOR/GUEST ENVIRONMENTAL, SAFETY & HEALTH GUIDELINE
PERFORMANCE EVALUATION
osw 10796*1
WATER_PCB-SD0000021669
OTHER GUIDELINE
#7
USE OF ANIMALS IN RESEARCH FACILITIES
The company will ensure that all animals used in its research programs are involved in projects of
importance to society and that the animals receive humane and professionally competent care and
treatment.
<
7.1 Preamble
The company develops pharmaceuticals, consumer goods, agricultural and industrial products that are used to treat diseases, to grow food, and to better the quality of human life throughout the world. The company works to ensure that these products provide valuable benefits to society and are safe to use.
In conducting research to ensure product efficacy and safety, company scientists use a variety of new technologies such as computer models, cell culture systems and other processes to identify effective products early on and to detect potential health problems or undesirable side effects. However, these systems are limited because they do not fully represent the complex processes of the human body. For that reason, product research and evaluation requires the use of laboratory animals.
All company research with animals is conducted under the review and supervision of Animal Care and Use Committees (ACUC) appointed by senior management Each ACUC consists of scientists, veterinarians, at least one non-scientist and at least one person not affiliated with the company. The committees regularly report their findings to senior management and appropriate governmental regulatory officials.
The vast majority of animals used by company researchers are rabbits, rats and mice. Rodents account for over 90 percent of all research subjects. The remainder includes dogs, pigs, sheep, cattle, goats and occasionally monkeys. Laboratory animals are purchased from companies that raise animals specifically for research. Livestock are purchased from commercial farms. The company does nor buy animals from pounds or shelters.
7.2 Animal Research
The company requires all scientists, technicians and managers associated with animal research programs to be fully cognizant and supportive of the specifics and spirit of this guideline.
The facilities and management programs established to support company animal research are directed and monitored by an attending doctor of veterinary medicine. The company's programs are fully accredited by the American Association for the Accreditation of Laboratory Animal Care (AAALAC).
73 Procedures
All company research animals are assigned to a specific protocol under the direction of a principal investigator. Before research can commence, each protocol is reviewed according to procedures prescribed by governmental regulations and adhered to by the ACUC. Each protocol is then reviewed and approved by an attending veterinarian and the ACUC. Records of research use and routine care are maintained for each animal. The company's goal is to give the highest consideration to the well-being of all animals used in research.
MONSANTO COMPANY
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7.4 Facilities
The company conducts all animal research in modem, well-maintained facilities that meet or exceed all regulatory standards. The company's animal facilities are considered to be among the best in the industry. Housing spaces include special facilities to quarantine newly arrived animals, isolation facilities, and conventional holding rooms to care for required animals. Room temperature, humidity, ventilation, lighting and other environmental conditions are carefully monitored and controlled.
7.5 Regulatory Review
The company is registered with the United States
Department of Agriculture as a research facility. Under
the provisions of die Animal Welfare Act, the
company's facilities are regularly inspected, aiid the
company flies an annual report
'
7.6 Information Requests
General information on the company's policy and procedures regarding animals used in research may be requested from Monsanto Corporate Communications. 800 N. Lindbergh Blvd., St. Louis, Missouri 63167. The phone number is (314) 694-7233. In general, the company's animal research facilities are not open to the public. However, visits and tours can be arranged by contacting the above address. Because of the nature of the research work under way, the company may restrict access to certain areas to ensure the health and safety of the animals. Recordings, filming, taping, photography and related activities are prohibited except as specifically approved.
(Revised and approved by the Environmental Policy Committee, October 22,1992.)
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OTHER GUIDELINE
#8
OZONE-DEPLETING CHEMICALS (CFC'S)
The company will initiate actions at all ofits worldwide sites to minimize the uses and environmental
releases ofthe chemicals subject to this guideline. It willseek out acceptable substitute chemicals,
when possible, on or before applicable compliance dates set by the site's local country laws and
regulations.
'
8.1 Scope
The following chemicals are those listed in the Montreal Protocol and are the minimum number subject to this guideline. Each company site should add to the list any other chemicals of local country concern and treat them according to this guideline in conformance with local country laws and regulations.
CFC-ll CFC-12 CFC-113 CFC-114 CFC-115 Halon-1211 Halon-1301 Halon-2402 CFC-13 CFC-111
CFC-112 CFC-211 CFC-212 CFC-213 CFC-214 CFC-215 CFC-216 CFC-217 Carbon tetrachloride Methyl chloroform
Company sites subject to this guideline include plants, offices, R&D facilities, sales offices, warehouses and farms, when the company owns or operates facilities or equipment that use or contain one of the chemicals subject to the guideline. This coverage includes any subsidiary in which the company is a greater than SO percent owner.
MONSANTO COMPANY
8.2 Program
The management of each worldwide site will do the following, where applicable:
8.2.1 Develop an inventory of uses and/or equipment containing any of the chemicals subject to this guideline.
8.2.2 Establish for compliance with this guideline a plan that contains the following minimum elements:
For refrigeration equipment, replace ibe___ refrigerant with an acceptable substitute when the equipment needs to be replaced or the original refrigerant is no longer available.
For explosion suppression and fire extinguishing equipment, replace the suppression or extinguishing chemicals subject to this guideline with an acceptable substitute when the equipment needs to be replaced or the original such chemical is no longer available. Provisions should also exist to provide for such chemical replacement after a system discharge, where practical.
After Jan. 1,1994, no new refrigeration, explosion suppression, or fire extinguishing equipment will be purchased that contains any chemical subject to this guideline, if substitute chemicals are reasonably available.
_
DSW L0796J
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For process and other uses of chemicals subject to this guideline, the company will expeditiously develop plans to cease using such chemicals by Jan. 1,1996.
In advance of any applicable laws and regulations, all sites will institute best management practices to minimize the uses
. ..and environmental releases of any chemicals subject to this guideline and seek opportunities for the use of acceptable substitute chemicals.'where possible, consistent with good business practices and employee safety/health considerations.
(Revised and approved by the Environmental Policy Committee, October 22.1992.)
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OTHER GUIDELINE
. #9
ENVIRONMENTAL, SAFETY AND HEALTH COMPLIANCE AUDITING
The company will conduct environmental, safety and health compliance audits to confirm that site management systems are in place to ensure continuous improvement and compliance with both governmental regulations and corporate, operating unit, and subsidiary policies and procedures.
9.1 Scope
Environmental, safety and health (ESH) compliance auditing will be conducted at all worldwide manufacturing and research sites.
9.2 Criteria
Each operating company and subsidiary will be responsible for ensuring that audits are conducted in accordance with the following criteria:
9.2.1 ESH compliance auditing programs will be
consistent with the five-step auditing approach as
outlined by the outside consulting firm of Arthur
D. Little and follow protocols approved by the
corporate ESH staff.
-........ ..
9.2.2 ESH compliance auditors will be appropriately trained, knowledgeable of the subject they audit, and skilled as compliance auditors.
9.2 J ESH compliance auditors will be independent of the location/site they audit
9.2.4 ESH compliance audits will be performed on a three-to-five year maximum cycle. The frequency for each site will depend upon the results of the last audit the degree of risk, complexity, and compliance issues at the site. The audit frequency for each site will be reviewed by the Environmental Policy Committee.
9.2.5 Reports of the actual audit findings and/or recommendations will be reviewed by appropriate legal staff and distributed, at a minimum, to site managers, directors of manufacturing (or equivalent for non manufacturing locations), legal and the corporate Quality and Compliance Assurance staff.
9.2.6 Follow-up on audit findings/recommendations will be the responsibility of each operating company and subsidiary. The corporate Quality and Compliance Assurance staff will request periodic status reports of auditing and follow-up corrective actions for communication to upper management
(Revised and approved by the Environmental Policy Committee, October 22,1992.)
MONSANTO COMPANY
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WATER PCB-SD0000021674
PROCEDURE
#1
EMPLOYEE HEALTH AND EXPOSURE COMMUNICATIONS
It is the company's intent to identify hazards ofchemical substances and physical agents in the workplace and to communicate such hazards to employees who may be exposed.
1.1 Responsibilities
Identification of health hazards of chemical substances,
physical agents, and biological agents in the workplace
is the joint responsibility of site management, the
directors of Environmental Operations (DEOs) and
corporate Environmental, Safety and Health (ESH). Line
management is responsible for the necessary communi
cations to and education and training of employees on
such hazards.
..
Europe/Africa Specific: The director of the Department of Medical Health and Safety (DMHS) Europe/Africa also assumes responsibility tor the necessary communications within Europe/Africa. In Europe, the DEO is represented by the director. Environmental and Regulatory Affairs. Other countries/regions may specify additional functions who share responsibility. - -
1.2 Employee Communication, Education and Training Concerning the Hazards of Substances in the Workplace
All employees whose work provides potential exposure to a hazardous chemical substance will have ready access to reference material, such as a Material Safety Data Sheet (MSDS), and will receive training in the nature of the hazards and appropriate wort: practices, protective measures and emergency procedures. Such training will be provided to employees when newly assigned to an area with potentially hazardous exposures and annually thereafter.
U Employee Access to Medical and Exposure Records
Access to an employee's medical or exposure records (if generated) will be provided within IS working days after the oompany receives a request in person or in writing from that employee, or as required by law if more stringent.
In addition to individual medical and exposure records,
an employee may have access to general exposure records
(such as area samples) for his/her work area and the
individual exposure records (with all identifiers deleted)
of other employees in the same work environment Since
much of the data requires interpretation or explanation,
the most appropriate physician or nurse should be
present during the review of medical records, and the
industrial hygienist or industrial hygiene contact should
be present during the review of exposure records to
provide such interpretation and consultation.
-
Written requests for medical and exposure records will be kept at the location bousing the records.
1.4 Other Communication of Exposure Information
Employees who participate in individual (personal) industrial hygiene monitoring will be informed of the sampling results.
All employees in an area where ambient air concentrations or physical agents are monitored should be informed of area concentrations, their relationship to relevant federal, state or local permissible exposure limits, the company's guidelines, and intended corrective action where required.
United States Specific: For certain substances, OSHA regulations require written notification to the employee.
MONSANTO COMPANY
DSh . n
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1.5 Communication of Physical Examination and Medical Test Data to the Employee
An employee will be informed about results of health evaluations and medical tests.
Copies of medical information will be sent to private
physicians upon the employee's request and only with
written authorization.
.
United States Specific: The employee will be informed in writing about results of health evaluation performed for occupational surveillance.
1.6 Employee Inquiries
Any employee inquiry about work exposures must be addressed by site management. The location physician, industrial hygienist or other appropriate management representative(s) should meet with the employee and provide a specific response based on the factual information available. The appropriate DEO, manager. Human Resources, and corporate ESH representative should be consulted in any non-routine situation.
EuropeJ'Africa Specific: The director of DMHS Europe/Africa should be consulted in any non-routine situation in Europe/Africa.
'
1.7 Communication of Health Studies
When employees have been involved in epidemiology or other health studies conducted by or on behalf of the company, an executive summary of the study results prepared by corporate ESH will be communicated in writing to the responsible DEO and site managers.---------Communications with the employees win be coordinated by the corporate DEO. The DEO may ask ESH and/or Europe Environmental and Regulatory Affairs (ERA) staff to develop a Communications Document and Dissemination Plan in consultation with plant personnel. A decision will be made at that time as to the total population to be included in the communication.
Other studies known to the company which are scientifically sound and which present significant new information concerning the potential hazards of a material to workers should be communicated to employees who have potential exposure to the substance. Where possible, employees should learn about significant potential hazards of materials with which they work from the company, and not from outside sources. However, a multitude of
epidemiological, animal and other health studies are conducted annually by the company and by others. These studies vary widely in terms of new knowledge provided, scientific validity, conclusiveness of the findings, applicability to humans or the work environment, etc. Location management in consultation with the DEO and corporate ESH and DMHS Europe/Africa (for Europe/Africa sites) should communicate in writing any applicable, reliable study results.
In determining where the results of a study should be communicated, factors such as the following should be evaluated:
the scientific validity and conclusiveness of the study;
whether the study produced new results of significance;
the applicability of tbe study to employees;
the significance of any potential hazard identified: and
___ tbe plans for follow-up studies.
When there is a question of whether the results of a study are significant enough to be communicated to appropriate employees corporate-wide, the matter will be referred to the following administration by any member of concerned management' The director of Medical and Health Sciences, Industrial Hygiene director. Corporate Toxicology director. Epidemiology director. Medical director, appropriate DEO and the assistant general counsel. Environmental Law. The appropriate Directors of Manufacturing, Human Resources and Public -..... Affairs/Relations will also provide consultation. A draft Communication Document and Dissemination Plan will be developed upon request, initially within ESH, to ensure that tbe study results are properly interpreted and that the communique will be properly reviewed and disseminated to all operating units and/or plants. The DEO, with support from corporate Industrial Hygiene and DMHS Europe/Africa (when Europe/Africa sites are involved) will transmit draft statements, announcements and supporting data to tbe appropriate location management
1.8 Access to Employee Medical or Exposure Records by Designated Representatives
A designated representative with the appropriate written authorization from the employee will be provided access to an employee's medical and exposure records within 15 working days of receipt of the authorization. A
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designated representative is any individual or organization to whom the employee has given written authorization to have access to the employee's medical or exposure records for a specific purpose on a specified occasion.
United States Specific: OSHA rules require that an employee's recognized or certified collective bargaining agent will be treated as a designated representative without regard to written employee authorization with respect to access to employee exposure records (with all identifiers deleted) and analyses of group medical and exposure records only. Final reports of completed epidemiological studies of unionized employees will be provided to the union involved on specific written request Information on the study results will be provided to all affected employees in a timely manner if this has not been done previously.
The appropriate managers. Human Resources and ESH representatives (DMHS Europe/Africa when Europe/Africa sites are involved) and the assistant general counsel. Environmental Law, should be advised of requests for access to records from a designated representative.
An OSHA inspector who presents a written access order approved by the Assistant Secretary of Labor for OSHA will be given immediate access to records specified by the order No order is required for access to exposure records. Requests should be reported immediately to the assistant general counsel. Environmental Law. Requests by NIOSH have been supported by the courts but should be cleared by the assistant general counsel. Environmental Law, before being granted. Reference should be made to 29 CFR Part 1910 Access to Employee Exposure and Medical Records, Final Rule 9 29-88.
1.9 Notification to Employees of Right of Access
Each location should make such notification of the existence, location and right of access to medical and exposure records a pan of its new hire orientation program and should post or otherwise inform all employees of this information and right each year.
1.10 Employee Health and Exposure Communications Plans
Each manufacturing and laboratory location should have written Employee Health and Exposure Communications Plans which address such things as those as follows:
the communication of and training on the hazards of chemical substances and physical agents in the workplace and proper handling methods, protective measures and emergency procedures:
the handling of employee inquires and expressions of concern about exposures;
the handling of employee and designated representative requests for access to medical and exposure records;
the communication of abnormal physical exam/medical test findings;
the regular communication of the industrial hygiene program and of exposure levels vs. standards;
the identification of materials or other subjects needing special communications efforts and plans for development of such programs locally or with the help of DMHS or others; and
notification to employees of their right of access to their medical and exposure records.
1.11 ESH Responsibility for Communication Programs
When its specialized expertise and/or a general communications need deem it appropriate, corporate ESH has a responsibility to develop a Communication Document and Dissemination Plan upon request for new health hazard information. The appropriate DEOs and management at representative plants will be consulted in the development of such plans to make them more suitable and effective for plant use.
'Europe/Africa Specific: Europe Environmental and Regulatory Affairs will be responsible for developing a Communication Document and Dissemination Plan which is appropriate for the laws and customs governing handling of employee health and exposure information in those countries.
1.12 Definitions
Access to Records: Consists of an opportunity to review an employee's medical and exposure records on site, and if requested, receipt of or opportunity to make a copy of the records. Unless otherwise specified by law, trade secret information may be deleted from the records provided to an employee or designated representative but they must be so informed that this was done.
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Medical Records: Include reports of physical examinations, medical tests tad other medical information on the employee in the company's possession.
Exposure Records: Include records of an employee's
wort: history and the level of exposure to potentially
harmful or toxic substances or agents and analyses of
such records.
'
Epidemiology Studies: Defined as scientific investigations of potential relationships between workplace exposures and health outcome of company employees or other occupational populations, as outlined in a study protocol.
(Revised and Approved: Vice President, Environmental, Safety and Health, October 22,1992.)
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PROCEDURE
. #2
TRANSMITTAL TO THE UNITED STATES ENVIRONMENTAL PROTECTION AGENCY OF SUBSTANTIAL RISK INFORMATION UNDER THE TOXIC SUBSTANCES CONTROL ACT
The company's procedure for handling the reporting ofinformation to the United States Environmental Protection Agency (USEPA) under the 8(e) substantial risk section ofthe Tbxic Substances Control Act (TSCA) as follows:
2.1 Abstract of Requirements
TSCA Section 8(e) requires any person (company) wbo manufactures, processes or distributes in commerce a chemical substance or mixture and who obtains information which reasonably supports the conclusion that such substance or mixture presents a substantial risk of injury to health or the environment shall immediately inform the EPA of such information.
2.2 Who Is responsible for reporting?
The requirements of Section 8(e) of the TSCA apply to "any person who manufactures, processes, or distributes in commerce." It is the company's position that the "person" wbo engages in the commercial activity is only the business organization, whether a sole proprietorship, corporation, partnership or association.
2.3 How are 8(e) reporting decisions made?
Company organizations that might receive TSCA 8(e) information will have a designated individual to whom such information shall he communicated. At least annually, the director of regulatory management (DRM), Toxic Substances, will publish a list of the designated individuals.
Anyone obtaining information of the type given in the abstract of requirements and detailed by EPA in their TSCA Section 8(e) Reporting Guide, dated June, 1991, should immediately submit such information to their supervisor. The supervisor shall immediately relay the information to the location or department manager, whichever is applicable, who, in turn, transmits it to the
proper designated individual in the organization. The information is then transmitted directly to the director of Medicine and Health Sciences.
It is imperative that the flow of information through this transmittal chain be rapid. In the event of nonavailability of a member of the communication network at the time information is first obtained, such member should be bypassed in the interest of speed.
All individuals involved in submission of substantial risk information to the director of Medicine and Health Sciences should keep a record of date of receipt and pertinent identifying details.
The director of Medicine and Health Sciences; environ mental counsel; DRM. Toxic Substances; and the appropriate operating unit directors) of environmental operations will comprise the designated official 8(e) committee to make decisions with respect to information that must be reported to the EPA under Section 8(e) of the TSCA.
Appropriate senior management will be informed of committee decisions.
In the event that a committee decision is not unanimous, the next appropriate level of management shall be consulted, and the matter will be resolved at the highest level, if necessary.
Employees who submit information through company channels will be notified of action taken by the 8(e) committee together with reasons for such action.
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In the event that, after the company has evaluated information and has determined that the item is not reportable under Section 8(e), the company becomes aware that an employee, as an individual, subsequently reported the item to the EPA. the company should review the situation to determine what action, if any, it should take with the EPA.
2.4 How are employees notified of 8(e) requirements?
All exempt company employees and others so designated by their organizational unit (plant nurses, contract physicians, scientists and engineers, etc.) within organizations that might receive or have access to TSCA 8(e) information, shall be informed of the provisions of Section 8(e). Annual reminders of 8(e) requirements will be provided to said employees. Records documenting the information communication will be maintained by the DRM, Toxic Substances.
(Revised and Approved: Vice President, Environmental, Safety and Health, October 22,1992.)
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PROCEDURE
#3
RECORDING ALLEGATIONS OF SIGNIFICANT ADVERSE REACTIONS UNDER THE TOXIC SUBSTANCES CONTROL ACT
The company's procedure for handling the Recordkeeping Requirements ofthe United States Environ mental Protection Agency's (USEPA) Final Rule Under Section 8(c) ofthe Tbxic Substances ControlAct (TSCA) is as follows:
3.1 Abstract of Rule
Manufacturers and certain processors of chemical substances and mixtures must maintain records of significant adverse reactions to health or the environment alleged to have been caused by a substance, mixture, article, process, effluent or emission. These records are subject to USEPA inspection.
Rule Reference - 40 CFR Part 717 (48 FR 38178 August 22,1983)
ii. Was a manifestation of a toxic effect after a significantly shorter exposure level than described.
iii. Was a manifestation of a toxic effect by an exposure route different from that described.
c. "Significant adverse reactions" are reactions that may indicate a substantial impairment of normal activities, or long-lasting or irreversible damage to health or the environment
Note: The Rule does not apply to pesticides, food, food additives, drugs or cosmetics when manufactured, processed or distributed for these uses.
3.2 Key Definitions
-
33 Exemptions from the Rule that Relate to the Company
a. Activities involving solely mining or other solely extractive functions.
(See Section 717.3 of the Rule for complete listing of definitions.)
b. Significant adverse reactions that are known human effects.
a. "Allegation" means a statement made without formal proof or regard for evidence, that a chemical substance or mixture has caused a significant adverse reaction to health or the environment
c. Significant adverse reactions to the environment directly attributable to incidents of environmental con tamination that have been reported to the United States federal government under any applicable authority.
b. "Known human effect" means a commonly recognized human health effect of a particular substance or mixture described in:
L Scientific articles or publications abstracted in standard reference sources.
ii. The firm's product labeling or material safety
data sheets (MSDS).
.
However, an effect is not a "known human effect" if it:
i. Was a significantly more severe toxic effect than previously described.
3.4 Who Can Receive an Allegation?
Allegations can come from a variety of sources including employees, contractors, customers and neighbors.
As a result, the company's receiving network must be broad. Initial receptors include plant, laboratory and other company location supervision, plant and other company location managers, the company's medical community at all locations, the offices of the operating company directors of Environmental Operations, sales and marketing contacts, switchboard operators at all locations, and environmental network contacts.
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3.5 Procedure for Handling Health or Environmental Allegations
The company's Toxic Substances Control Act (TSCA)
Section 8(c) procedure consists of a four-step review
and decision process. A determination than an allegation
is not recordable under the Rule can be made at any step
in the process. The procedure is shown schematically on
Appendix 3.3.2.1
.
a. Step One - Each plant or other company-designated locations or laboratory will have at least one identified and trained TSCA Section 8(c) key contact The director of Environmental Operations (DEO) or designee from the appropriate operating companies, representatives of the Business and Research Support Services (BRSS), and director, regulator management (DRM), Toxic Substances, will serve as the key contacts for the General Office. The DEOs have responsibility under this procedure for free standing divisions and subsidiaries of which the Co*, pany owns SO percent or more of the voting stock or other equity rights, or for which the company has the power to control the management and policies of that firm. At Step One, all initial receptors will automatically transfer persons making oral allegations to the key contact at their locations. Initial receptors will also transfer written allegation to the key contact at their location. There are two exceptions with respect to oral allegations: If the initial receptors are either members of the department of Medicine and Health Sciences Occupational Medicine (DMHS-OM) group (physicians) or the DEO's office, then these individuals may judge at Step One if an oral allegation is excluded. Decision criteria for Step One: pesticides, food, food additives, drugs, or cosmetics are excluded. If a decision is made that the allegation is excluded, the allegation, if written, will be discarded and, if oral, will not be acted txi under this procedure.
If the allegation is oral and not excluded, the key contact will inform the alleger that such allegation may be recordable under the Rule and request that the alleger submit a written and signed allegation to the key contact. Monsanto Form 8(c)A, shown on Appendix 3.2, is available to be used for all employee related oral health allegations and can be used at the discretion of the DEO for external oral health allegations. All key contacts must note on a written allegation the date of its receipt.
b. Step Two The key contact at a company location or the appropriate DEO for the General Office will pro vide company employees with Form 8(c)A for oral allegations of health effects. Written allegations will then be reviewed by the key contact, who will then make a Step Two decision. The key contact will deter mine if the written allegation is exempted from the Rule using the criteria in Step One. If a decision is made that an allegation is exempt from the Rule, the allegation will be discarded. Otherwise, the allegation will be sent to the appropriate DEO for review.
c. Step Three - The appropriate DEO will serve as the coordinator for Step Three and Step Four activities. Allegations received from the location (e.g. plant, etc.) key contacts will be reviewed by the DEO and a Step Three decision made. A Step Three decision will also be made by the DEO or other General Office key contact regarding allegations made to the General Office receptors. If the Step Three decision is that the allegation is not recordable under the Rule, the allegation will be discarded. Otherwise the allegation will proceed to Step Four.
d. Step Four - The DEO will form a committee to make decisions with respect to allegations that must be recorded under the Rule. The committee will be chaired by the DEO and consist of the appropriate members of DMHS-OM for human effects, appropriate members of Environmental Sciences staff for environmental effects. Environmental Law staff, and the DRM, Toxic Substances. If the decision is that the allegation is not recordable under the Rule, the allegation will be discarded. The DEO will provide feedback to the location key contact If the Step Four decision is that the allegation is recordable under the Rule, than the DRM, Toxic Substances, will place the allegation and documents mandated by the Rule in the TSCA Section 8(c) file. The DEO will provide feedback to the location key contact.
3.6 Recordkeeping
The TSCA Section 8(c) file will be kept in the Office of the DRM, Toxic Substances. The file structure will con form to requirements of Section 717.15 of the Rule. Files pertaining to adverse reactions to health of employees will be retained for 30 years. Files pertaining to other adverse reactions will be maintained for five years.
lA separate procedure for litigation claims (Appendix 3.3.1) and the company's Wear-Dated Hotline (Appendix 3.3.3) will be used.
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3-7 Communications a. Disposition of written allegations will be communi
cated back to the individual making tbe allegation. The key contact will facilitate tbe communication. b. A summary of the TSCA Section 8(c) procedure will be periodically communicated to all affected employees and updated, as appropriate.
(Revised and Approved: Vice President, Environmental, Safety and Health, October 22,1992.)
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Appendix 3.1
SIMPLIFIED FLOW DIAGRAM OF MONSANTO PROCEDURE FOR HANDLING ALLEGATIONS SUBJECT TO TSCA 8(c)
STEP ONE: Decision
Not subject to TSCA 8(c) recordkeeping. Drop from process.
Note: Initial Receptors may be key contact. DEO office is also a key contact.
STEP FOUR: ---------Decision
Allegation qualifies for TSCA 8(c) recordkeeping. Put in 8(c) file in St. Louis
PR3. Page 4 of 8 Company Confidential
Send written allegation and Forms 8(c)A to St Louis
i
DEO Office
DEO forms an 8(c) review committee
1
8(c) Committee
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STEP TWO: Decision
Not subject to TSCA 8(c) recordkeeping. Drop from process.
STEP THREE: Decision
Not subject to TSCA 8(c) recordkeeping. Drop from process.
STEP FOUR: Decision
Not subject to TSCA 8(c) recordkeeping. Drop from process.
WATER PCB-SD0000021684
TO: SITE KEY CONTACT
Form 8(c)A 11/92
Appendix 3.2 REPORTING FORM FOR ALLEGATIONS OF SIGNIFICANT ADVERSE REACTION TO HEALTH
Toxic Substances Control Act, Section 8(c) 40 CFR Part 717
NAME OF ALLEGER:_____ ADDRESS: (If not employee)
DATE;//
MO DAY
YR
SITE LOCATION:
SITE LOC. CODE:
(If health effect only): M F
YR. OF BIRTH: _
Employer (if other than Monsanto): _________________________________________
DESCRIPTION OF ALLEGED AVERSE HEALTH EFFECT: 1. WHAT IS THE HEALTH EFFECT BEING CLAIMED? __________________
2. HOW LONG DID IT LAST?
3. HOW OFTEN HAVE YOU EXPERIENCED EFFECT?
4. IN WHAT WAY DID IT AFFECT YOUR NORMAL ACTIVITIES?
5. HOW WERE YOU EXPOSED?
WHAT SUBSTANCE, MIXTURE, PROCESS OR OPERATION DO YOU THINK CAUSED THE EFFECT YOU DESCRIBED:
FOR COMPANY USE ONLY: RECEIVED ON: BY:
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Appendix 3.3.1
TSCA 8(c) RECORDKEEPING: LITIGATION CLAIMS
Detailed Procedure:
Sup 1
'
Litigation complaints will be reviewed at the time of receipt by the law department for relevance to TSCA 8(c) recordkeeping. Criteria for this review include the following:
a) Is the claim against a Monsanto product or process?
b) Is the product(s) in question one that is covered by TSCA, i.e., other than pesticide, herbicide, food, food additive or pharmaceutical?
c) Is the claim a health or environmental claim?
If all criteria is met. the claim will be sent to the DMHS occupational medicine group. Exceptions to this include claims against the Agricultural Group, Nutrition and Health Care Products that will be sent to these respective groups when the law department is unsure of the answer to question (b).
Step 2
The occupational medicine group of DMHS will review the litigation claims passed to them by the law department The
review will be based on EPA's definitions of "known human effect" and "significant adverse reactions" (40 CFR 717).
For environmental effects, DMHS may need to contact the appropriate DEO for assistance. Claims that do not meet
TSCA 8(c) criteria will be dropped from further TSCA review of this step. Those claims that meet TSCA 8(c) criteria
will be forwarded to the DRM, Toxic Substances, for filing.
-
Step 3
Claims meeting the 8(c) criteria will be filed in the TSCA 8(c) file maintained by the DRM, Toxic Substances. This office will request a copy of the complaint, abstract, and "answer" from the law department
Step 4
The law department will forward a copy of the complaint, abstract, and "answer" to the DRM, Toxic Substances, for filing in the TSCA 8(c) file, along with the "complaint." The "complaint," abstract and "answer" will constitute the TSCA 8(c) recordable "allegation" and "follow-up" for all litigation filings.
A block flow diagram of the TSCA 8(c) process for litigation complaints appears on the reverse side of this page.
(Revised 10/22/92)
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Appendix 3.3.2
TSCA 8(c) REVIEW PROCEDURE OF LITIGATION CLAIMS
Request "Answer"
*
Law Department
"Answer** I
DSH 107982
DRM TSCA
File "Answer" in 8(c) file
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Appendix 3.3.3
TSCA 8(c) RECORDKEEPING: WEAR-DATED HOTLINE
Detailed Procedure:
Step 1 All health and environmental effect allegations received by the Wear-Dated hotline will be documented by the phone operator on a standard foi'm.
Step 2
The documented health and environmental effect hotline call will be reviewed by the Chemical Group Product Safety department for TSCA 8(c) relevance.
Step 3
'
The hotline allegations that are judged by the Chemical Group Product Safety department as meeting TSCA 8(c) recordkeeping requirements will be forwarded to the DRM, Tbxic Substances, for filing.
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#4
PREMANUFACTURE NOTIFICATION TO UNITED STATES ENVIRONMENTAL PROTECTION AGENCY UNDER THE TOXIC
SUBSTANCES CONTROL ACT
The company's procedure for development ofpremanufacture notification (PMN) to the United States Environmental Protection Agency (USEPA) as required under Section 5 ofthe Toxic Substances Control Act (TSCA) is as follows:
4.1 Abstract of Requirements
A PMN is required to be submitted to USEPA for all new chemical substances at least 90 day before the substance can be manufactured for commercial purposes. A number of substances are exempted from these requirements. including, but not limited to drugs, food and food additives, pesticides, RAD substances, nonisolated intermediates, and substances on the TSCA inventory.
Final Rules Reference - 40 CFR Part 720.
4.2 Is a PMN Required?
At a very early stage of new product development, including isolated intermediates and new imports, several checks should be made to determine if a PMN will be required for the product.
4.2.1 Is the Product (Substance) Exempt under TSCA?
Responsibility: Operating unit director. Environmental Operations (DEO) or designee.
Section 2(B) of TSCA exempts broad classes of substances such as pesticides, food, food additives, mixtures and others.
* The PMN rule exempts small quantities for RAD purposes and has provisions to exempt substances for test marketing low volume manufacture and for polymer manufacture.
The rale also exempts impurities, some by-products, articles and nonisolated intermediates.
Refer to TSCA law and regulations or the company's PMN manual for details or contact operating unit DEO or designee or director, regulatory management (DRM), Toxic Substances (TSCA).
4.2.2 Is the Substance "New" under TSCA? (Is It on the TSCA Inventory of Chemical in Commerce?)
Responsibility: Operating Unit DEO or designee.
Contact the operating unit DEO or designee and have the TSCA non-confidential inventory searched for the substance.
If the substance is on the TSCA nonconfidential inventory, it is not new under TSCA definition and a PMN is not required. If the substance in question is not on the nonconfidential inventory, the confidential inventory must be searched.
To search the confidential inventory, a Bona Fide Intent to Manufacture (BIM) notice must be submitted to USEPA. A copy of the instruction for submitting a BIM can be found in 720.25 of 40 CFR 720. Send a copy of the BIM to the DRM, TSCA for corporate recordkeeping purposes.
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If USEPA reports that the substance is not on the confidential inventory, then the substance is a new substance under TSCA and a PMN is required unless the material is exempt under Section 2 (a) above.
43 What Information Is Required on a PMN
Submission?
Final rules detailing the PMN requirements can be found in 40 CFR 720. All PMNs must be submitted on USEPA Form 7710-25 (1/91). Copies of the form and instructions for its use are available from the DRM, TSCA. The required PMN information falls into either the category of General Information or Risk Assessment Data. USEPA will accept additional data-in many cases, it is desirable to submit Risk Analysis, pollution prevention data or other information to assist USEPA with their assessment. Since the company performs a Risk Analysis on all new products via the Pledge Guidelines and the EC-201/202 procedures, the information is available for this purpose.
4.4 What Are the Details of the PMN Procedure?
The PMN process should be integrated into the
.
development scheme of a new project In most cases, the
PMN development will be initiated during the earliest
phases of commercialization of a product. The PMN
must be submitted to USEPA at least 90 days before the
product can be manufactured for commercial purposes,
including test marketing.
4.5 How Is a PMN Initiated?
Responsibility: Operating unit DEO or designee.
The operating unit contact submits an ER-200 or EC-201 to the Department of Medicine and Health Science (DMHS) if one has not already been submitted (See company booklet G-2738 for ER-200 and EC-201/202 Procedures).
The operating unit contact drafts a PMN using the USEPA form.
The operating unit contact calls a scoping meeting. Minimum participants at the meeting are operating unit contact, operating unit DEO or designee (if not serving as a contact), member of corporate Environmental Sciences center or other qualified environmental effects expert (if appropriate). DMHS toxicologist and DRM. TSCA. Copies of PMN drafts, along with an
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approved ER-200 or EC-201 for the substance are supplied to participants in advance. Note: The scoping meeting can be bypassed at the discretion of the operating unit DEO.
At the scoping meeting, decisions are made by the operating unit contact, as to the scope and detail of optional information to supply. If optional risk analysis is desired, assignments are made to DMHS toxicology, industrial hygiene, etc., to complete the necessary sections. A decision is also made as to whether an EC-202 is needed before a PMN submission. Note: It is appropriate at this stage ofproduct development to initiate a Material Safety Data Sheet (MSDS) and a TFS37for label andfreight classification.
4.6 How Are PMNs Finalized?
Responsibility: Operating unit DEO or other designated operating unit contact.
The operating unit contact prepares a final draft using input from the scoping meeting as well as follow-up input from DMHS.
The operating unit contact, together with the patent department, reviews the final draft for confidential information and develops appropriate confidentiality claims with substantiation, where necessary.
The final draft is circulated to the participants of the scoping meeting for final review.
The operating unit contact calls a meeting for final comments/approvals if needed.
4.7 How Are PMNs Submitted?
Responsibility: DRM, TSCA After final review/approval, the operating unit
contact forwards the PMN to the DRM, TSCA (authorized official), for submission.
The DRM, TSCA, will submit the PMN (both confidential and non-confidential as appropriate), using applicable USEPA submission requirements.
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4.8 How Is USEPA Follow-up on a PMN Handled?
Each PMN will identify a technical contact in addition to an authorized official. The technical contact will typically be operating unit DEO, Commercial Develop* menu or R&D contact
4.8.1 PMN Fees
A S2.500 fee is required for all PMNs, except intermediates filed at the same time as final product (SI ,000) or exemptions (zero cost).
A unique six-digit TS-user fee identification must be assigned to each PMN and must also appear on the check.
The fee is sent to a separate USEPA office from the PMN.
4iU2 Phone Contact
All calls from the USEPA on technical matters should be handled by the "Technical Contact."
All verbal questions concerning nonconfidential inquiries by the USEPA may be discussed at the time of call or deferred to obtain an answer if unknown or if unsure as to USEPA authority to ask for the information.
Non-confidential oral responses may be followed up with a written response when deemed appropriate by the contact In all cases the technical contact should write a note to file documenting the conversations, with a copy to the DRM, TSCA.
Confidential inquiries previously discussed with the USEPA or claimed confidential in the PMN may de discussed at the discretion of the technical contact
All other verbal confidential questions will be addressed by written response only.
Verbal response to USEPA will be followed up, at the discretion of the technical contact, with a written letter documenting the conversation and clearly indicating areas of confidentiality, with a copy to the DRM, TSCA.
4.8.3 EPA Actions
,
Responsibility: The operating unit DEO or
designee will have prime
responsibility, with counsel
of Environmental Law and
the DRM. TSCA.
USEPA may extend the review period by an additional 90 days.
USEPA may ask for more information under Section 5(e).
i. An order may be issued by USEPA.
ii. A consent order may be jointly agreed upon. The consent order can include restriction on manufacture or use in lieu of information generation.
USEPA may restrict manufacture or use under Section 5(f).
4.9. How Is the Company Follow-up on the PMN Submission Handled?
Responsibility: Operating unit DEO or designee.
The company may request USEPA to stop the clock on PMN reviews at any time during the review period.
After USEPA's review period expires, manufacture can commence at any time, subject to any 5(e) or 5(0 restrictions. A Notice of Commence to Manufacture (NCM) must be submitted to USEPA within 30 days of the first manufacture for commercial purposes. The information to be included in the notice are detailed in 40 CFR 720. Confidential claims must be made again at this time, as appropriate. Send a copy of the NCM to the DRM, TSCA for corporate recordkeeping purposes. Once a NCM is filed with USEPA, the PMN substance is placed on the TSCA inventory.
(Revised and Approved: Vice President, Environmental Safety and Health, October 22,1992.)
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#5
OCCUPATIONAL FATAL ACCIDENT REPORTING
In case ofa fatal accident, the company's Lav Department must be contacted in addition to following government, operating company, and corporate-reporting requirements.
OSHA regulations require that, within 48 hours after the occurrence of an employment accident which is fatal to one or more employees or which results in bospitalization of five or more employees, the employer of such employee(s) shall report the accident either orally or in writing to the nearest office of the OSHA Area Director. The reporting may be by telephone or telegraph. The report shall relate the circumstances of the accident, the number of fatalities, and the extent of any injuries.
In such instances the following guidelines are considered necessary to protect the civil rights of company employees.
In addition to routine operating company and corporate notifications in fatal accidents, either Mary M. Tonkin or Michael E. Gewin (for accidental deaths) or L. William Higley (for deaths for long-term chemical exposure), the company's attorneys for OSHA matters, must be notified immediately. The telephone numbers are listed below. They will provide prompt necessary legal guidance including, where necessary, sending an attorney to the site for on-the-spot counseling.
In the meantime, OSHA inspectors) should be given access to the site of the accident when the inspector arrives on the premises, without requiring that the inspector secure a warrant for entry. However, neither members of location management nor any wage employee should discuss the accident with the OSHA inspector until advised to do so by the company attorney.
The location manager or his designee will greet the inspector and state that location employees have been asked not to discuss the accident until the company attorney advises them accordingly.
The inspector is to be told that we have been forced to take this posture as a result of the OSHA Procedure for Investigating Criminal/Willful Violations. The inspector will be permitted to inspect the plant, and, of course, should be advised of any chemical hazards and protective measures needed, related or not to the accident
Location personnel will not allow the inspector to view any records or documents at this time, other than the lost-time injury log, OSHA Form 200 and Form 101 or its equivalent until advised to do so by the company attorney.
If the location is requested to rope off the area of the accident, local discretion should be exercised. The inspector, however, is not authorized to keep plant management away from any part of the operation.
If local management believes entry by the inspector must be delayed for a few hours because of exposure, safety, confusion, etc., management will seek such a recommendation from Ms. Tonkin or Mr. Higley at the time of the initial call to St. Louis.
Contacts Mary M. Tonkin, 314/694-2967 (office), (314) 721-8209 (home).
Michael E. Gewin, 314/694-2849 (office), (314) 352-2176 (home).
L. William Higley. 314/694-8503 (office); (314) 862-1796 (home).
(Revised and Approved: Vice President. Environmental, Safety and Health, October 22,1992.)
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PROCEDURE
#6
TRANSMITTAL OF TOXICOLOGY AND HEALTH-RELATED DATA TO UNITED STATES REGULATORY AGENCIES
Health-related information should be submitted through the Department ofMedicine and Health
Sciences.
The various regulatory agencies are continually supplied
information from toxicology and health-related tests on
the company's products done by or for die company. In
order to provide consistency in the handling and review
of such information, as well as to assure proper follow-
through on commitments to these agencies, the
transmittal of such test results will be carried out in
accordance with the following guidelines:
.
6.1 All toxicology or health-related data will be reviewed with the department of Medicine and Health Sciences (DMHS) prior to submission to any regulatory agency, except for routine submissions by the company's Agricultural Group of test data required under the Federal Insecticide, Fungicide, and Rodentidde Act (FIFRA). In addition, DMHS will be informed of all such submissions at the time via the letter of transmittal.
6.2 Any such information transmitted must be recorded and the copy of the final submission retained both by DMHS and the involved operating company.
6.3 The letter of transmittal for any toxicology or health-related data must include a listing of the materials being transmitted including sufficient bibliographic information for subsequent retrieval of the original data.
6.4 If the submission includes data on human health effects, it is preferable that the information be submitted to the regulatory agency by the director of the depart ment of Medicine and Health Sciences.
6.5 Agreements with a regulatory agency that commit the company to the future transmittal of toxicology or health-related data must also be reviewed and approved in advance by DMHS; further, DMHS must concur with the feasibility of meeting commitment dates. Appropriate records of such commitments must be maintained both by the involved operating company and DMHS in order to ensure future compliance with such agreements.
6.6 Any exceptions to the above must be approved by the director of DMHS.
(Revised and Approved: Vice President. Environmental, Safety and Health, October 22,1992.)
MONSANTO COMPANY
OSH 107988
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Company Conndential
WATER PCB-SD0000021693
REFERENCE: Cross Reference ESH Worldwide Guidelines, Pledge Guidelines, and Responsible Care
ESH Worldwide Guideline
Effluent and Emission Control Waste Management Plant Environmental Assessments
Employee and Community Safety and Health
Pledge Guideline Pollution Prevention
Responsible Care
Code on Pollution Prevention Practices No. 1 through No. 11. except No. 4 and No. 8
Employee And Community Safety and Health
Code on Process Safety, Employee Safety and Health and Community Awareness and Emergency Response
None (Internal Process Safety
and Emergency Response Policy Elements)
Product Stewardship
Process Safety and Emergency Response
Product Stewardship
Code cm Process Safety Code on Community Awareness and
Emergency Response
Code on Product Stewardship
None (Internal Distribution Policy
Elements)
Chemical Distribution
Code on Distribution
Waste Management - Corrective and Remedial Action
Plant Environmental Assessments
Groundwater and Soil Quality
Outside Processors
Outside Processors
Code cm Pollution Prevention, Practices No. 13 and No. 14
Code on Pollution Prevention, Practices No. 12
Code on Pollution Prevention. Practices No. 12
None
(Internal Policy Elements on Public Participation and Involvement)
Community Awareness at Manufacturing Sites
Code on Community Awareness and Emergency Response, Practices No. A1 - No. A9
Code on Pollution Prevention Practices No. 4 and No. 8
DSW 107989
REFERENCE Company Confidential
WATER PCB-SD0000021694
Responsible Care:1' A Public Commrtment
GUIDING PRINCIPLES
Member companies of the Chemical Manufacturers Association are committed to support a continuing effort to improve the industry's responsible management of chemicals. They pledge to manage their businesses according to these principles:
To recognize and respond to community concerns about chemicals and our operations. To develop and produce chemicals that can be manufactured, transported, used, and disposed of safely. To make health, safety and environment considerations a priority in our planning for all existing and new products and processes. To report promptly to officials, employees, customers and the public, information on chemicalrelated health or environmental hazards and to recommend protective measures. To counsel customers on the safe use. transportation and disposal of chemical products. Tp operate our plants and facilities in a manner that protects the environment and the health and safety of out employees and the public. To extend knowledge by conducting or supporting research on the health, safety and environmen tal effects of our products, processes and waste materials. To work with others to resolve problems created by past handling and disposal of hazardous substances. To participate with government and others in creating responsible laws, regulations and standards to safeguard the community, workplace and environment To promote the principles and practices of Responsible Care* by sharing experiences and offering assistance to others who produce, handle, use. transport or dispose of chemicals.
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OSH i.C799i
WATER PCB-SD0000021696
Responsible Care:f A Public Commitment
SUMMARY DESCRIPTION
RESPONSIBLE BARE* PROGRAM ELEMENTS
The statement of Guiding Principles for Responsible Care* is a commitment ov eacn member company to fully support a continuous effort to improve the industry'rresponsible manage ment of cnemicais Each member company has pledged to operate according to tne Guiding Principles and has signed to that effect. The signed statement is considered an obligation of membership m the Chemical Manufacturers' Association |CMA|.
The Guiding Principles are based on CMA's 1983 policy statement on health, safety and the environment and on the Canadian Responsible Care4 principles. They also incorporate guidance received from member company executive contacts.
Following association adoption of the Guiding Principles, various CMA committees began developing Codes of Manage ment Practices in January 1989. Each Code of Management Practices addresses several public concerns. Impetus for developing a specific Code comes from either a substantial
public concemis) identified by the Public Advisory Panel or the industry, a substantive need to take voluntary action, or both. Codes m development address community awareness and emergency response, distribution, pollution prevention, process safety, employee health and safety, and product stewardship. The Codes of Management Practices identify expected manage ment practices as obiectives rather than prescribing absolute or Quantitative standards. Since the Codes are intended to serve as objectives, they complement existing member company programs or practices that achieve the same goals. Responsible Care*, therefore, becomes an integral part of existing company programs and will cause each company to stretch to continually improve performance
Another important element in the Responsible Cara* initiative is the Public Advisory Panel which is composed of a group of environmental, health and safety thought leaders. The panel is an industry (CMA) effort, not a company responsibility,
it was assembled and is moderated by an experienced facilitator working at the association's direction. It serves to assist the industry in identifying and developing programs and actions that are responsive, and are viewed as responsive, to public con cerns. Meeting several times a year, the panel reviews issues on which CMA requires comment and advice. Panel members also identify areas they believe require-industry response, critique all proposed Codes of Management Practices and provide early definition of public concerns involving the chemical industry. Community Advisory Panels at the local or regional level can serve companies and the industry in a similar manner CMA has developed guidance to facilitate companies formation and operation of local panels.
Effective performance evaluation is a critical element of Responsible Care* Therefore each Code of Management Practices includes a Self-Evaluation Form that measures a company s improveo use of tne management practices that the Code defines Memoer companies will conouct self-evaluations
for each Code annually CMA will compile tne results arc periodically report industry s collective implementationoreg'ess
to the public. To document progress in ways that are meaningful to tne
public,CMA also will monitor statistical trend data wners available, on industry performance. For example. Suoerfunc Section 313 emissions reporting and Department of Transporta tion hazardous materials incident statistics will be a component of public reporting for the Pollution Prevention Code and tne Distribution Code.
Oue to their varying size and operations, member companies will not be expected to be at the same level of performance for each Code of Management Practices at the same time However, it is expected that each member company report continued progress.
To facilitate and support each member company's continual improvement in the responsible management of chemicals. Executive Leadership Groups (ELGs) have formed ELGs provide an opportunity for corporate leaders to discuss progress and share experiences with implementing elements of Responsible Care*. These regional groups of ten to twenty executive contracts will meet at least once a year to review Codes of Management Practices under development discuss members' progress with implementing existing Codes, identify areas where individual companies need assistance from CMA or other companies, and to address other priority industry issues
Endorsement of the Responsible Care* initiative is an Obligation of Membership in the association. A member
company's obligation to Responsible Care* applies to all of its chemical business. Each member company is expected to make a
commitment to Responsible Care* by: a) signing the Guiding Principles of Responsible Care*' b) communicating the commitmeot to Responsible Care* to
employees: c) making good-faith efforts to implement the Codes of
Management Practices, participate in the self-evaluation process, and meet the expectations of the Responsible Care* initiative: and d) using the Responsible Care* name and logo according to
CMA's guidelines. Member companies are also expected to participate m the
development of the Codes and programs. In an extreme case, where a member company has consis
tently not conducted its operations in accordance with the Guiding Principles and program elements of Responsible Care* association representatives will meet with the member company's executive contact to seek the company's positive involvement in the program. If this fails to produce a commit ment to Dursue the objectives of Responsible Care*. aoDropnate actions will be taken including the disassociation of tne company from membership
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osw 10 7993
WATER PCB-SD0000021698
Responsible Care:1 A Public Commitment
QUESTIONS AND ANSWERS
ABOUT RESPONSIBLE CARP
Q Who had the idea for the Responsible Care* initiative?
A. Executives of the Canadian Chemical Producers Association (CCPA) began Developing the concept-m 1984. Executives of Chemical Manufacturers Association ICMA) member companies that have Canadian operations brought Responsible Care* to CMA's attention. CMA considered a variety of options and adopted the performance-based Responsible Care* initiative in 1988.
Q How is Responsible Cere* different from what the chemicel industry has been doing?
A. Many chemical companies have programs that are designed to improve performance. However. Responsible Care* is a broad chemical industry commitment to improve performance through a process that ensures responsiveness to the public's concerns. Two aspects make Responsible Care* unique. Fust bylaws obligate CMA member companies, representing 90% of basic industrial production capacity in the United States, to participate in the initiative. And second, through a Public Advisory Panel, the public is directly involved in developing program elements.
Current CMA programs such as Community Awareness and Emergency Response ICAER). Air Quality. Waste Minimization, and National Chemical Response and Information Center (NCRIC) are vital parts of the initiative. Through Responsible Care' s self-evaluation process and Public Advisory Panel. CMA will identify areas where additional resources need to be developed to help member companies achieve the goals of the initiative. Responsible Care* also encourages member companies to help each other improve performance by sharing experiences and resources in specific areas of chemical operations.
Q Why does the chemicel industry need to do anything?
A. Because in spite of past efforts there still are too many incidents involving chemical operations. Politicians and government regulators will respond to the public's concerns about chemicals artfour industry if the chemical industry does not respond first Therefore, it is important for the industry to take continuing positive action to address public concerns.
Q Isn't there some other way? The chemical industry is already doing a lot can't h fust communicate this?
A. The CMA membership concluded that the chemical industry doesn't ;ust have a public relations problem, it has a perfor mance problem. The chemical industry has to respond effectively to public concerns through improved performance It is dear mat the public's expectations are not being met on a
performance basis. Until the chemical industry truiv understands public concerns and addresses them for a perfor mance standpoint CMA member companies can t possibly improve the public perception of their inoustry
Q Who prepared tho Guiding Principles and what are they based on?
A. The guiding Principles are based on CMA's 1983 boardapproved policy on "Health. Safety and the Environment" and the Canadian Responsible Care* principles. They are consistent with both. They were prepared by representatives of CMA member companies and approved by the CMA Board of Directors.
Q Why don CMA's Board think Rnponsiblo Care ` will work?
A. Since Responsible Care* is based on concepts proven m both the Canadian experience aod CMA's voluntary programs such as CAER. the CMA membership has confidence that it can achieve improved industry performance. Most important by signing me Guiding Principles. CMA member companies have demonstrated their commitment to make Responsible Care* work.
Q How much will Rosponsiblo Care* cost CMA member companies to implement?
A. Significant resources are needed from member companies, both in terms of the 'sweat equity* of participants in the development and support of the program, and in the people and dollars necessary to mate the initiative 'live* In each company.
These costs have not been quantified because they will be different for each company. However, overall industry costs for Responsible Care* implementation will undoubtedly add to the bil.hons of dollars already being spent by industry to manage health, safety, and environmental issues.
Q Why should a commhmonl to Rosponsiblo Cara* be an obligation of momborehip?
A. Public concerns about chemicals and the industry are the result of collective experience with the entire industry. If the chemical industry is to respond to public concerns effectively, it must act as a total industry; Responsible Care* must be visibly working throughout the industry and. therefore, must be both a commitment and a membership obligation of every company in the association, ft is critical to achieve the cultural change needed for. the industry to improve performance in a responsive manner. The public must be convinced that the chemical industry is living up to its commitment.
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WATER_PCB-SD0000021699
Q Why have a Public Advisory Panel?
A. Resoondmg to Duoiic concerns is what Resoonsibie Care' is
ail aoout Therefore a xev component of the initiative is tne
PuDnc Aovisorv Panel The Dane! neios the moustrv ioentifv ano
oeveico orograms and actions that are resoonsive to public
concerns aocut soecmc oerformance .orooiems
CMA nas also ceveiopec a guioeoook for companies which
wisn ;o estaonsn community aovisorv panels at operating
locations
Q Who is on the Public Advisory Panel? Who sets it up?
Can panel members be replaced.
A. The Public Advisory Panel acts as a sounding board for public concerns ano as a specially qualified focus group that directly impacts industry policies and programs under Responsible Care1 Meeting five times a year, panel members help CMA identify puoic concerns ano suggest ways to respond to those concerns. Panel members also review proposed Codes bf Management Practices and evaluate other features of the initiative. Each meeting is managed by an outside facilitator experienced with panel management Industry representation is kept to a minimum to encourage an open exchange of views and ideas.
Currently, the panel is a 15-member group composed of individuals from both public and private sectors. To ensure that a wioe range of public opinion is expressed, the composition of the panel is diverse. Occupations and interests of members range from business and local government officials to environ mental. academic, and consumer activists, a fanner, and an expert in business ethics.
Panel members were selected by the facilitator. Panel membership will penodically change in response to pane! members' availability and/orihe changing needs of penei expertise. The facilitator will handle such changes.
Q Who wiH develop the Codos of Management Practices? Will the public have imput?
A. The development of Codes of Management Practices begins with the identification of public concerns by a number of sources, including the Public Advisory Panel antKMA's Board of Directors. CMA reviews .these concerns and recommends priorities for Code development. If a public concern cuts across a range of company operations or activities, it maybe addressed by more than one Code
CMA member company experts develop each Code. Every memoer company has opportunities to comment on the Codes through open meetings and workshops. Public input to the codes is achieved through the Public Advisory Panel. All codes, once approved by CMA's Board of Directors; are made available to others. Use of the Responsible Care* service mark, however, must follow CMA's guidelines and can be used only with CMA approval.
Q Will Responsible Care* Codes of Management Practices become the besis for future legislation end regulation?
A. A very positive result of Responsible Care* should be for its meaningful and workable practices to be reflected in legislation or regulation that the public endorses through government anion.
Q How will performance against the practice Codes be measured? Who does the measuring and how are the results reponed?
A. 'noiviouai comoanv management wn> e-.anjctf :*e
performance against the Cooes of Manaceme-t -*2::
annuallv bv fiimc out a seif-evaiuation term -or sac' Ccce
Companies will ieed this information cacn tc CMA s-.r.c~. _se
of such feedback would De to direct trie asscc atior s sjcccwork to areas of tne greatest need ano mgr.es: Detent,5 Cv-
the longer term-, these aggregate reports sncuic estac-s* 5
record of improvement thatwitt enaofe .MA re
--
industry's performance progress to the pudhc
Q What will CMA do to help companies address the Codes of Management Practices?
A. CMA will develop support programs to help companies implement the practices defined in the Codes in general, programs and aids (videotapes, guide-books, educational meetings, etc.) will be similar to the support prov<deo for Tme m: and CAER. A unique element of Responsible Care' is ;r.at member companies will help each other by sharing resources and methods they develop to implement the Codes of. Management Practices.
Q Given the kind of data wa era reporting under Title III. will the public accept the Responsible Cera ` initiative new?
A. Disclosures under Title III raise the level of public concern significantly in some cases. But their only effective response is to deal with the concerns through company and industry-wide improvements. This is the essence of Responsible Care* The experience in Canada and in the United States suggests it can work.
B Will chemical companies apply tha initiative outside the United States?
A. CMA represents North American manufacturers and can best assist its members in implementing Responsible Care* here However, the initiative is already international in scope. CMA learned from a two-year old Canadian effort Other countries that have officially adopted Responsible Care* initiatives include Australia. New Zealand. England. Germany. The Netherlands, and France.
CMA's experience with CAER suggests that good initiatives spread rapidly. The United Nations, with U.S. chemical industry assistance, has already developed an international emergency response program modeled on CAER.
CMA has shared Responsible Care* materials with counter pan organizations in Europe. Japan. Australia, and Taiwan.
Page 6 of 98
OSW 1-07995
WATER PCB-SD0000021700
Responsible Care: A Public Commitment
COMMUNITY AWARENESS AND EMERGENCY RESPONSE CODE OF MANAGEMENT PRACTICES
Purpose:
The goal ofthe Community Awareness and Emergency Response (CAER) Code ofManagement Practices is to assure emergency preparedness and to foster communityright-to-know. It demands a commitment toopenness and community dialogue. The code has two major components: first, to assure that member facilities that manufacture, process, use, distribute or store hazardous materials initiate and maintain a community outreach program to openly communicate relevant, useful information responsive to the public's questions and concerns about safety, health, and the environment; and second, to help protect employees and communities by assuring that each facility has an emergency response program to respond rapidly and effectively to emergencies.
The community outreach component will communicate program activities and performance under all codes of management practices and will promote an open, ongoing dialogue with employees and the community. Information should be provided about such activities as waste minimization, emission reduction, health effects of chemicals, and efforts to ensure the safe transport of chemicals.
The CAER Code ofManagement Practices is supported by, and will build on, CMA's CAER process. CAER supports the community's right to know about chemical industry operations and their effect on safety, health, and the environment CAER originally was a voluntary initiative focused on emergency response issues. Ihe new CAER Code ofManagement Practices broadens the facility-community dialogue to cover the full range of safety, health and environmental issues.
Relationship to Guiding Principles:
The Code helps achieve several of the Responsible Care Guiding Principles:
Q To recognize and respond to community concerns about chemicals and our operations.
To report promptly to officials, employees, customers, and the public, information on chemical-related health or environmental hazards and recommend protective measures.
To participate with government and others in creating responsible laws, regulations, and standards to safeguard the community, workplace and environment.
To promote the principles and practices of Responsible Care by sharing experiences and offering assistance to others who produce, handle, use, transport, or dispose of chemicals.
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WATER_PCB-SD0000021701
CAER Code of Management Practices November 6. 1989 -- Page 2
Management Practices; A. Community Awareness and Outreach
Member facilities that manufacture, process, use, distribute or store hazardous materials shall have a community outreach program that includes:
F*r Employees: '
--
- -...................
L An ongoing assessment of employee questions and concerns about the facility.
2. Communications trainingfor key facility and company personnel who communicate with employees and the public concerning safety, health, and environmental issues.
3. Education of employees about the facility's emergency response plan and safety, health, and environmental programs.
4. An ongoing dialogue with employees to respond to their questions and concerns and involve them in community outreach efforts.
5. A regular evaluation ofthe effectiveness ofthe ongoing employee communications efforts.
For Community:
.
6. An ongoing assessment of community questions and concerns about the facility.
7. An outreach program to educate responders, government officials, the media, other businesses and the community about the facility's emergency response program and risks to the community associated with the facility.
8. A continuing dialogue with local citizens to respond to questions and concerns about safety, health, and the environment, and to address other issues ofinterest to the community.
9. A policy of openness that provides convenient ways for interested persons to become familiar with the facility, its operations, and products, and its effortsto protect safety,health, and the environment
10. A regular evaluation of the effectiveness of the ongoing community communications efforts.
B. Emergency Response and Preparedness
'
Member facilities that manufacture, process, use, distribute or store hazardous materials shall have an emergency response program that includes:
1- An ongoing assessment of potential risks to employees and local communities resulting from accidents or other emergencies.
2. A current, written facility emergency response plan which address, among other things, communi cations and the recovery needs of the community after an emergency.
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CAER Code of Management Practices November 6. 1989 -- Page 3
3. An ongoing training program for tboae employees who have response or communications responsi bilities in the event of an emergency.
4. Emergency exercises, at least annually, to test operability of the written emergency response plan. 5. Communication of relevant and useful emergency response planning information to the Local ___ Emergency Planning Committee. 6. Facility tours for emergency responders to promote emergency preparedness and to provide current
knowledge of facility operations. 7. Coordination of the written facility emergency response plan with the comprehensive community
emergency response plan and otherfacilities. Ifno plan exists, the facility should initiate community efforts to create a plan. . 8. Participation in the community emergency response planning process to develop and periodically test the comprehensive community emergency response plan developed by the Local Emergency Planning Committee. S. Sharing ofinformation and experience relating to emergency response planning, exercises, and the handling of incidents with other facilities in the community. MEMBER SELF-EVALUATION Each member company shall report annuallyto CMA, orits designated agent, the stage ofimplementation of each Management Practice in this Code. The reports shall be on the member self-evaluation form attached as Exhibit A.
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OSK 107998
WATER PCB-SD0000021704
Member Sel/-Evaluation
January 8. 1992 Pagc 1
Responsible Care: A Public Commitment--
CHEMICAL MANUFACTURERS ASSOCIATION MEMBER SELF-EVALUATION FORM
COMMUNITY AWARENESS AND EMERGENCY RESPONSE CODE OF MANAGEMENT PRACTICES
Member Company Name:__________ Responsible Carcfl Coordinator Name: - ... ... .. -----------Address:
Telephone ( )________________ Number of facilities subject to code
OSH 10799.9 R, Page U of 98
WATER_PCB-SD0000021705
Member Self-Evaluation January 6. 1992 -- Page 2
COMMUNITY AWARENESS AND EMERGENCY RESPONSE CODE OF MANAGEMENT PRACTICES
Instructions:
__ _ _ Under theTlesponaible Care Initixtivercachmamber companywiDsubmitaSelf-Evaluation form
annually to CMA. To establish the industry baseline, each member company should complete this Self
Evaluation form,
'
2. Indicate on the cover page the number ofmember company facilities subject to the Code. Each company must report the implementation category for all facilities subject to the Code on this form.
3. For each Management Practice on the following four pages, indicate the number of facilities that have attained each implementation category. Each facility should appear in only one milestone category per Management Practice. The total number of facilities subject to the Code should equal the number of facilities across all six implementation categories for each Management Practice.
4. Only subject facilities owned or operated as of the reporting date should be included.
5. The implementation categories are:
Category NA Category EV -
Category DP Category IA Category PP Category RI
No action. Ifno action taken because the management practice is not applicable, please explain. Evaluating axisting company practioaa against the Msnsgemant Practice. Developing plan to implement Management Practice. Implementing action plan Management Practice in place. tUasseeemg Management Practice implementation.
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CAER Code of Management Practices January S. 1992 -- Page 3
Management Practices
rategnrin
Community Awareness
NA EV DP IA PP RI
1. An ongoing assessment of employee concents and questions about the facility.
Comments on Category NA:.
2. Communications training for key facility and company person nel who will communicate with employees and the public con cerning safety, health and environmental issues.
Comments on Category NA:.
3. Education of employees about the facility's emergency response plan and safety, health, and environmental programs.
Comments on Category NA:
_________________
4. An ongoing dialogue with employees to respond to their ques tions and concerns and to involve them in community outreach efforts.
Comments on Category NA:
5. Aregular evaluation ofthe effectiveness ofthe ongoing employee communications efforts.
Comments on Category NA:
CtUf7 KA
Ctiforj rv
Catagor7 DP Calagavy IA Catafary CaUfoiy XI
Xa actiam. g--aettaa taSaaSaea--i tt# --aafmawt j--etlaa la--t aypSeaMa. pi--aa aplal. Xralnatlaf aalatiaf --vpasy pnctle-- agaiaat tka Maaafaa--t Pnedaa. Davalopiaf plaa ta hnplamant Maaagunanf hactlaa. Tmplimanrtwf aetlaa plaa Haaafa--t PikUm la placa.
aim1iS Maaafaxaast Practi-- i~ - latlaa
DSM 106000
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WATER_PCB-SD0000021707
CAER Code of Management Pracucea January 8. 1992 -- Page 4
Catreoriw NA EV DP IA PP Ri
6. An ongoing assessment of community questions and concerns about the facility.
7. An outreach program to educate responders, government offi cials, the media, other business, and the community about the facility's emergency response program and risks to the commu nity associated with the facility. Comments on Category NA:
8. A continuing dialogue with local citizens to respond to questions and concerns about safety, health, and the environment, and to address other issues of interest to the community. Comments on Category NA:
9. A policy of openness that provides convenient ways for inter ested persons to become familiar with the facility, its operations, and products, and its efforts to protect safety, health, and the environment. Comments on Category NA:
10. A regular evaluation of the effectiveness ofthe ongoing commu nity communications efforts..
Comments on Category NA:______ ________________________
CaUtwyJU
Category EV Category DP
Cotogeay 1A PP
C*U|ot7 XJ
Itooctloa. Em Mtai Ukoa Smmm tko Svaloatlaf ultCU| rsmpany proctlcaa agataat Ik* Dmlaylai pin to tniplamaal boplomantlag actio* pin Maai|tmaat Practice ta phn. Scaaiaaetug SiaqiaMt Practlea
it practlea la aat appScabla. plaaaa arplatn
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DSW 108001
WATER PCB-SD0000021708
CAER Code of Management Practices January 6. 1992 -- Page 5
Emergency Response 1. An ongoing assessment of potential risks to employees and local
communities resulting from accidents or other emergencies.
Tommemron Category NA_
Qugnrig
NA EV DP 1A PP RI
2. A current, written facility emergency response plan which
address, among other things, communications and the recovery needs of the community after an emergency.
Comments on Category NA:
3. An ongoing training program for those employees who have response or communications responsibilities in the event of an emergency.
Comments on Category NA*.
4. Emergency exercises, at least annually, to test operability ofthe written emergency response plan..
Comments on Category NA*
5. Communication of relevant and useful emergency planning information to the Local Emergency Planning Committee.
Comments on Category NA*
ctufrM
Calagary gV Catafory DO Category 1A
Catafwry W Catafoiy 91
K* aetlam. V M ictka Ukw tirmi tka waaagamaat fneUti U sat appttcabia, plaaaa rplln
ajdattag aaapaay ynetleaa against tka ktaaagamaat Pnctfaa.
Drraloplag plan ta twplamaat Mnugaiaml Practtaa.
haplanantlng acttaa plan
Maaagamaat fiutkt ta plana.
at Ptactlaa
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WATER_PCB-SD0000021709
CAER Code of Management Practices January 8. 1992 -- Page 6
lUjjUj(S
NA EV DP IA PP Rl
6. Facility tours for emergency responders to promote emergency
preparedness and to provide current knowledge offacility opera*
tions.
.
Comments on Category NA:.
7. Coordination of the written facility emergency response plan with the comprehensive community emergency response plan and other facilities. If no plan exists, the facility should initiate community efforts to create a plan. Comments on Category NA:,
6. Participation in the community emergency response planning process to develop and periodically test the comprehensive community emergency response plan developed by the Local Emergency Planning Committee. Comments on Category NA:
9. Sharing of information and experience related to emergency response planning, exercises, and the handling ofincidents with other facilities in the community. Comments on Category NA:
Notes: Please identify any specific problems and/or resources.
CUf7 XA Cal agwry XV CiH|wy DP Catagory IA Catagory W Catagory KJ
Page 16 of 98
!( tetlaa. Ha* teSw Ukta bacaoaa thi mtat|Mt practico la awt applicable. plaaaa wpUla, Xralaatlas arUttwg napujynditM afataat tka HanafiaiMl riaillaa Davalaplag plaa ta implement Maaafamaat Practlea. laplaaatta| actioa plaa MaAagamaat Practiea la placa. Kaaaaaaatng Maaagamant Practlea fanpWountitjaa.
DSW 108003
WATER PCB-SD0000021710
Responsible Care: A Public Commitment
DISTRIBUTION CODE OF MANAGEMENT PRACTICES
Purpose
The purpose of the Distribution Code ofManagement Practices is to reduce the risk ofharm posed by the distribution ofchemicals to the general public; to carrier, distributor, contractor and rhomirnl industry employees; and to the environment. Adherence to the code will lead to continually safer chemical distribution and help member companies to: evaluate the risks associated with chemical distribution and methods to reduce those
risks; meet or exceed all regulations and industry standards governing chemical distribution; provide emergency advice and/or assistance to people on the scene in the event of a
chemical distribution emergency, develop new technologies and methods to improve chemical distribution safety. The code will also promote improvements in: employee preparedness and awareness in preventing distribution emergencies; the safety performance of carriers and other providers of distribution services; the public'6 preparedness in responding to chemical distribution emergencies;
OSH 108004
R. P*ge 17 of 98
WATER_PCB-SD0000021711
Distribution Code of Management Practices January 15,1991 -- Page 2
the public's understanding of, and confidence in, industry efforts to improve chemical
distribution safety.
The Distribution Code of Management Practices applies to all modes of transportation
(highway, rail, marine, air and pipeline) and to the shipment of all chemicals, including
chemical waste. The code also applies to distribution activities (storage, handling, transfer
and repackaging) while chemicals are in transit between member companies and their
suppliers andcustomers. The implementation of a number ofpractices of the code will vary
according to the characteristics ofthe chemicahbeing distributed, the mode oftransportation
and the type of distribution activity involved.
-_
Relationship tn Responsible Care Guiding Principles
This code helps achieve several Responsible Care Guiding Principles:
to recognize and respond to community concerns about chemicals and our operations;
to make health, safety and environmental considerations a priority in our planning for all existing and new products and processes;
to counsel customers on the safe use, transportation, and disposal of chemicals;
to operate our plants and facilities in a manner that protects the environment and the health and safety of our employees and the public;
to participate with government and others in creating responsible laws, regulations.and standards to safeguard the community, workplace and environment; and
to promote the principles and practices ofResponsible Care by sharing experiences and offering assistance to others who produce, handle, trse, transport or dispose ofchemicals.
Management Practices
Each member company shall have an ongoing chemical distribution safety program that includes senior management commitment through policy, communications and resources to improvements in chemical distribution safety. The program should indude the following elements:
1. Risk Management
1.1 Regular evaluations ofchemical distribution risks which consider the hazards ofthe material, the likelihood of acddents/inddents and the potential for human and environmental exposure from release of the material over the route of transport.
1.2 Implementation of chemical distribution risk reduction measures that are appro priate to the risk level.
Page 18 of 98
X)SW 106005
WATER_PCB-SD0000021712
Distribution Code of Management Practices January 15, 1991 -- Page 3
.
1.3 Internal reporting and investigation of chemical distribution accidents/inti denis, and implementation of preventive measures.
2. Compliance Review and Training
2.1 A process for monitoring changes and interpretations of new and existing regula tions and industry standards for their applicability to the company's chemical dis tribution actmties, and for implementing those regulations and standards,
2.2 Training for all affected company employees in the proper implementation of applicable regulations and company requirements.
2.3 A program for providing guidance and information to carriers, distributors and contractors who perform distribution activities for the company on the company's training and compliance requirements for the activities.
2.4 Regular reviews of company employee, carrier, distributor and contractor compli ance with applicable regulations and company requirements.
3. Carrier Safety
3.1 A process for qualifying carriers ofall modes and types (common, contract, private and customer controlled) that transport chemicals to and from company facilities that emphasizes carrier safety fitness and regulatory compliance, and includes regular reviews of their performance and compliance.
3.2 Feedback to carriers on their safetyperformance and suggestions for improvement.
4. Handling and Storage
4.1 Documented procedures for the selection and use ofcontainers that are appropriate for the chemical being shipped, in compliance with testing and certification requirements, and free ofleaks and visible defects.
4.2 Documented procedures forloading chemicals at companyfacilities thatwill reduce emissions to the environment, protect personnel and provide securement of the lading during transit.
4.3 Documented procedures for unloading chemicals at the company's facilities that will reduce emissions to the environment, protect personnel, and provide for safe unloading into proper storage facilities.
4.4 Defined criteria for the cleaning and return of tank cars, tank trucks, marine vessels, and returnable/refillable bulk and semi-bulk containers, and for the proper disposal of cleaning residues.
DSW 10800b
R, Page 19 of 98
WATER_PCB-SD0000021713
Distribution Code of Management Practices January 15,1991 - Page 4
4.5 A program for providing guidance and information to customers, distributors, and other receivers on proper procedures for unloading and storing the company's chemicals.
4.6 A process for selecting distributors and other facilities that store or handle the company's chemicals in transit that emphasizes safety fitness and regulatory com pliance and indudes regular reviews of their performance and compliance.
4.7 Feedback to distributors and operators-of other farilities that store or handle chemicals in transit on their safety performance and suggestions for improvement.
5. Emergency Preparedness
5.1 A process for responding to chemical distribution accident/incidents involving the
company's chemicals.'
.
5.2 Documented procedures for making information about the company's chemicals in distribution available to response agendes.
5.3 A program for making facilities and/or training materials available to emergency response agendes.
5.4 Dialogue with state and local emergencyplanningorganizations on the distribution and hazards of the company's chemicals to improve community preparedness to respond to chemical distribution emergenries.
5.5 Dialogue with the public on their concerns about chemical distribution safety, actions taken bythe industry and the company toimprovethe safety ofchemical dis tribution, and the effectiveness of emergency preparedness and emergency re sponse assistance.
Member Self Evaluation
Member companies shall report annually the stage ofimplementation ofeach management practice in this code to an agent designated by the Chemical Manufacturers Assodation.
Relationship to Other Codes of Management Practice
This Code complements, and should be implemented in cox^unction with, current and future Codes of Management Practices.
Page 20 of 98
OSVt 1080-7
WATER_PCB-SD0000021714
SAMPLE
A*
s*
Public Commitment
CHEMICAL MANUFACTURERS ASSOCIATION MEMBER SELF-EVALUATION FORM
DISTRIBUTION CODE OF MANAGEMENT PRACTICES
Member Company Name:_____________________
Responsible Care Cnordinator
Name:_____________________ Address:___________________
Telephone {__l
108008
R, Page 21 of 98
WATER_PCB-SD0000021715
R. Page 22 of 98
-OSW 108009
WATER PCB-SD0000021716
Member s>eii--vaiuauon form January 15, 1991 - Page 2
Member Self-Evaluation Distribution Code of Management Practices
1. Under the Responsible Care initiative, each member company must submit a Self Evaluation Form annually to CMA or its designated representative. The annual self reporting has three purposes:
to establish an industry baseline from which to demonstrate continual progress in implementation of the Code.
to assist individual member companies in establishing a base line from which to set priorities for future development; and
to assist the industry (CMA) in designing programs to assist the member companies in achieving the goals of the Responsible Care initiative.
2. TO ESTABLISH THE INDUSTRY BASELINE, EACH MEMBER COMPANY SHOULD COMPLETE THIS SELF-EVALUATION FORM AND SEND IT BY C.O.B., MAY 23, 1991
3. The Distribution Code is unique in the sense that it deals with both products and facilities, but more importantly it deals with a broad range of third party providers of services and many external organizations and communities. This is considerably different than the CAER, WARR and Process Safety Codes, which deal primarily with fixed facilities and, as a result, have a more common base for self-evaluation. In contrast, different self-evaluation bases for each element of the Distribution Code will likely be more helpful and appropriate.
4. Self-evaluations for the Distribution Code should be expressed as percentages since the different bases for Code elements may not always be countable units. Therefore, the evaluation of each ofthe 21 separate dements ofthe Distribution Code ofManagement Practices should show what percentage of the company's distribution process is at each of the six implementation stages. For example, for a specific Code element, a company could report that 10% of their distribution process is at stage 1,50% at stage H, 30% at stage III, 10% at stage IV and 0% at stages V and VI. Judgment will be required on how to develop these percentages, both in terms of what base to use for the calculation, and how to reflect centralized and/or decentralized distribution activities. Most importantly, each company will need to establish a methodology that will remain constant over the years in orderto measure annual progress. The suggestions under Item4 below are meant to assist you in developing your self-evaluation methodology.
5. The following bases for evaluation can be applied to a number of specific code elements:
Corporate programs, such as a corporate emergency response process, may be viewed as applying across the company for purposes of completing the Self Evaluation Form. The percentage implementation would result from judgment of
DSW lOflOlO
page 23 of 98
WATER_PCB-SD0000021717
Page 24 of 98
DSW 108011
WATER PCB-SD0000021718
Member Self-Evaluation Form January 15, 1991 -- Page 3
SAMPLE
the existence and implementation of that process, or progress upon your own implementation action plan.
Alternatively, decentralized programs, such as site or division specific emergency response processes, should bejudged as separate processes. A large multi-division company may have multiple emergency response processes to consider in establish ing a percentage ofimplementation.
Risk management activities are often undertaken on a product specific basis. ~Each company deals with a very large number ofproducts which are hazardous or nonhazardous, and must select a basis from which to evaluate and report future progress in implementing the Code. Judgmentis required to make sure that a large number ofnon-hazardous products which the company produces or distributes do not distort the evaluation. They should also not decrease the validity ofthe base for
future evaluations.
Carrier safety reviews should be based on the number ofcarriers that fall under the code. Judgment mustalsobe used where datais notreadilyavailable on all carriers. The time spent on determining this basis will provide good information for progressing toward full implementation.
The number of third party providers of services to your company can serve as the basis for determining percentages ofimplementation in each stage.
Customer related elements should be evaluated on the basis of the number of customers, the hazardous nature ofthe products, and/or by the company divisional or business unit programs.
There are some elements, such as loading and unloading procedures, that are site specific and should be evaluated on that basis.
6. It is recognized that self-evaluation methodologies will vary from company to company. Because of this, flexibility has been built into the evaluation process. The basis for evaluating a company's distribution process should be established, documented and applied consistently for each annual self-evaluation exercise.
7. The six implementation stages are:
Stage I - No action
Stage II - Evaluating company practices against Code practices Stage IH Developing action plan to implement Code practice Stage IV - Implementing action plan Stage V Code management practice in place Stage VI Implementation reviewed and reaffirmed this year
DSN 108012
R, Page 25 of 98
WATER_PCB-SD0000021719
Member Self-Evaluation Form January 15, 1991 -- Page 4
Risk Management PracticesIII HI IV V____________ VI
1.1 Regular evaluations of chemical dis tribution risks which consider the haz ards ofthe material, the likelihood of accidents/incidents and the potential
___ far -human and environmental exposure from release ofthe material over the route of transport.
----- --.
------------ -- ---
......-
1.2 Implementation of chemical distri bution risk reduction measures that are appropriate to the risk level.
1.3 Internal reporting and investigation of chemical distribution acddentsdnddents, and implementation of pre ventive measures.
Compliance Review and Training
2.1 A process for monitoring changes and interpretations of new and existing regulations and industry standards for their applicability to the company's chemical distribution activities, and for implementing those regulations and standards.
2.2 Trainingforall affected company em
ployees in the properimplementation ofapplicable regulations and nmpmy requirements.
2.3 A program for providing guidance and information to carriers, distributors and contractors who perform distribution activities for the company on the company's training and compliance requirements for the activities.
2.4 Regular reviews of company employee, carrier, distributor and contractor com pliance with applicable regulations and company requirements.
R. Pape 26 of 98
>SW 108013
WATER PCB-SD0000021720
Member Self-Evaluation Form January 15, 1991 -- Page 5
Carrier Safety
Im IV
3.1 A process for qualifying carriers ofall modes and types (common, contract, private and customer controlled) that transport chemicals to and from company facilities that -emphasizes carrier safety fitness and regulatory compliance, and includes regular reviews of their performance and compliance.
..... - . . . ...
--
V VI
-----------------
.
IsV *
i
3.2 Feedback to carriers on their safety performance and suggestions for im provement.
Handling and Storage
4.1 Documented procedures for the selec tion and use of containers that are appropriate for the chemical being shipped, in compliance with testing and certification requirements, and free of leaks and visible defects.
4.2 Documented procedures for loading chemicals at company facilities that will reduce emissions to the environ ment, protect personnel and provide securement ofthe lading duringtran sit.
4.3 Documented procedure far unloading chemicals at company facilities that will reduce emissions to the environ ment, protect personnel, and provide for safe unloading into proper storage facilities.
4.4 Defined criteria for the cleaning and return of tank cars, tank trucks, marine vessels, and returnable/refillable bulk and semi-bulk containers, and for the proper disposal of clean ing residues.
5 A program for providing guidance and information to customers, distribu tors, and other receivers on proper
DSW 108014
R. Page-27 of 98
WATER PCB-SD0000021721
Member Self-Evaluation Form January 15, 1991 -- Page 6
SAMPLE
Handling and StorageI______H_____ED_____IV_____V______VI
procedures for unloading and stor ing the company's chemicals.
4.6 A process for selecting distributors
and other facilities that store or handle
the company's-chemicals in transit that emphasizes safety fitness and
--
--------- --
regulatory compliance, and includes
regular reviews oftheir performance
and compliance.
4.7 Feedback to distributors and operators ofother facilities that store or handle chemicals in transit on their safety performance and suggestions for improvement.
-- ---.... - -
Emergency Preparedness
5.1 A process for responding to chemical distribution accidents/incidents in volving the company's chemicals.
5.2 Documented procedures for making information about the company's chemicals in distribution available to response agencies.
5.3 A program for making facilities and/ or training materials available to emergency response agencies.
5.4 Dialogue with state and local emer gency planning organizations on the distribution and hazards of the com pany's chemicals to improve commu nity preparedness to respond to chemi cal distribution emergencies.
5.5 Dialogue with the public on their concerns about chemical distribution safety, actions taken by the industry
and the company to improve the safety ofchemical distribution, and the ef fectiveness of emergency prepared
ness and emergency response assis tance.
R. Page 28 of 98
OSW L08015
WATER PCB-SD0000021722
Distribution Code of Practices Questions and Answers
1. What is the distinction between a distribution emergency and a distribution accident'
incident?
.
Answer: An accident/incident is a definite and distinct occurrence ofan undesirable event. It may involve an accident (traffic, derailment, collision, mishandling) ornearmiss, or be a result of a non-accidental container or operational failure. The undesirable effect can range from a small release of product (but major media coverage) to a m^jor release with subsequent loss of property or personal injury.
An emergency is simply an acddentfinddent that requires immediate action.
In the context ofthe code, we distinguish between the two because we have direct control or influence over the causes ofaccidents and incidents. Many circumstances that dictate the emergency nature ofthe situation are most often outside ofour sphere ofcontrol and influence.
2. The words process, program, documented procedures and defined criteria are used throughout the code. What do they mean?
Answer: A program is meant to mean an organized list ofprocesses and procedures. In developing a comprehensive distribution safety program the management practices ofResponsible Care should be included in the list ofprocesses and procedures. In a hierarchy ofterms, a program lies below a policy (a general statement of commitment or philosophy) and somewhere above a process or procedure. A program must address management needs, as expressed by policy, and contain feedback and measurement steps to determine ifthe need& are being met.
A process is a series ofrelated activities or actions that will lead to the desired end result. In the context ofthe code we have used process when it is dear the process can take many different forms, yet still provide the desired results.
Documented procedures are specific instructions or steps required to complete a task successfully. They may be written procedures or videotaped procedures, for example, that are to be explidtly followed and are notleft open to interpretation. They are the most detailed step in the heirarchy, below polities, programs and processes.
Defined criteria are the ground rules around which a process or a procedure must be developed. In the code, the term is used to provide criteria to a third party that would enable that party to develop a process or procedure to lead to the desired end.
D-Sk 108016
R. Page 29 o! 98
WATER_PCB-SD0000021723
Questions and Answers January 15, 1991 -- Page 2
3. Reference is made in the code to adherence to industry standards. What is meant by this0
.
Answer; The term industry standards, means those agreements, developed and complied with voluntarily, by a wide range ofco-producers, interindustry groups and trade associations.
Many of these agreements, in time, result in regulations or rulemaking procedures. It may also apply to a company's own internal standards of operation or practice.
4. The term, regular reviews, is used when referring to carrier safety performance, contractor and distributorperformance and regulatory compliance. What is meant bv the ~
term, regular review?
Answer: Regular reviews is a term used to measure or testwhether our expectations are being met.
They are crucial formanaging the whole distribution safely process. By regular, we allow room for periodic or random reviews and allow the company to determine its own frequency ofreview for each element ofthe code, where itis appropriate. Reviews can take
many forms, ranging from on-site and detailed audits, to presentations ofprogress with charts and graphs. This also allows incorporation of many of the safety performance reviews into quality and service review initiatives.
5. The code refers to cleaning and return ofretumable/refillable containers. What is meant by retumable/retillable?
Answer; Returnable containers are those containers specifically designed for return to the company for reuse without reconditioning or reworking the container. Generally,, this typically only applies to containers of 55 gallons and above. The EPA is developing regulations regarding refillable containers that would drop below 55 gallons. Tank trucks, tank cars and marine vessels may or may not normally return to the company. Often, they are cleaned and placed bade in general service.
All ofthe containers listed above are examples ofreturoable/refiHable containers. For the purpose of the Distribution Code we must define criteria aimed at developing proper cleaning and residue disposal of these containers. Non-refillable, non-returnable containers are not covered under code.
6. What is meant by regular evaluations of chemical distribution risks?
Answer;
How often distribution risk studies should be conducted will depend significantly on the chemical involved and the dynamics ofthe distribution. Evaluations should be regular in the sense they become a normal and routine part of distribution activities and are conducted often enough to respond to technology changes and operating experience.
Page 30 of 98
DSW 108016.01
WATER_PCB-SD0000021724
Questions and Answers January 15, 1991 - Page 3 7. The code requires dialogue with state and local planning organizations and the general
public. What do we mean by dialogue? Answer:
Dialogue is simply two-way conversation. It implies that both parties listen and respond to each other in a constructive way. With state and local planning organizations, the ___ dialogue will naturally focus on the more technical and factual aspects of chemical distribution. Dialoguewiththepublic will involve moreeducational types ofinterchange for both parties. (
DSw 108017 R. Page 31 or 98
WATER_PCB-SD0000021725
R. Page 32 of 98
osw loeoie WATER PCB-SD0000021726
April 6. I99TI
Amended ScfM^mhcr *. |W1
Responsible Care: A Public Commitment
POLLUTION PREVENTION CODE OF MANAGEMENT PRACTICES
Purpose. This Code is designed to achieve ongoing reductions in the amount or all contaminants and pollutants released to the air, water, and land from member company facilities. These reductions are intended to respond to public concerns with the existence of such releases, and to further increase the margin of safety for public health and the environment.
The Code is also designed to achieve ongoing reductions in the amount of wastes generated at facilities. These reductions are intended to help relieve the burden on industry and society of managing such wastes in future years.
In implementing the Code, each company should strive for annual reductions, recognizing that production rates, new operations, and other factors may result in increases. Despite these fluctuations, however, the goal is in establish a long-term, substantial downward trend in the amount of wastes generated and contaminants and pollutants released. Quantitative reduction goals will be established for giving priority to those pollutants, contaminants and wastes of highest health and environmental concern.
This code also includes practices that address the broader waste management issues beyond source reduction and other waste and release reduction efforts. Each member company must manage remaining wastes and releases in a manner that protects the environment and the health and safety of employees and the public.
This Code complements, and should be implemented in conjunction with current and future Codes of Management Practices. Key terms arc defined in the Glossary, which should be consulted for assistance in interpreting the provisions of this Code.
10801.9
R. Page 33 of 98
WATER_PCB-SD0000021727
Pollution Provtntlon Code . Peg# 2
Relationship to Guiding Principles
Implementation of this Code helps achieve the following Guiding
---- Principles;......
...................------------------:----------- ..--------------- ---- ----
o To recognize and respond to community concerns about chemicals and our operations;
o To develop and produce chemicals that can be manufactured, transported, used and disposed of safely.
o To make health, safety, and environmental considerations a priority in our planning for all existing and new products and processes;
o To report promptly to officials, employees, customers and the public, information on chemical-related health or environmental hazards and to recommend protective
measures.
o To operate our plants and facilities in a manner that protects the environment and the health and safety of our
employees and the public;
o To extend knowledge by conducting or supporting research on
the health, safety, and environmental effects of our products, processes, and waste materials.
o To promote the principles and practices of Responsible Care by sharing experiences and offering assistance to others
who produce, handle, use, transport, or dispose of chemicals.
o To work with others to resolve problems created by past handling and disposal of hazardous substances.
o To participate with government and others in creating responsible laws, regulations and standards to safeguard the community, workplace and environment.
o To promote the principles and practices of Responsible Care
by sharing experiences and offering assistance to others who produce, handle, use, transport or dispose of chemicals.
R. Page J4 of 98
OSU 108020
WATER PCB-SD0000021728
Pollution Prevention Code Page 3
Management Practices.
Each member company shall haw a pollution prevention program which shall include:
------- ------4.
A cjear commitment by senior management through policy,
communications, and resources, to ongoing fed unions at each or the company's facilities, in releases to the air, water, and land ana in the generation of wastes.
2. A quantitative inventory at each facility of wastes generated and releases to the air, water, and land,
measured or estimated at the point of generation or release.
3. Evaluation, sufficient to assist in establishing reduction
priorities, of the potential impact of releases on the
environment and the health and safety of employees and the
public.
*
4. Education of, and dialogue with, employees and members of the public about the inventory, impact evaluation, and risks to the community.
5. Establishment of priorities, goals and plans for waste and
release reduction, taking into account both community concerns and the potential health, safety, and environmental impacts as determined under Practices 3 and 4.
6. Ongoing reduction of wastes and releases, giving preference first to source reduction, second to rccyclc/rcusc. and
third to treatment. These techniques may be used separately or in combination with one another.
7. Measurement of progress at each facility in reducing the generation of wastes and in reducing releases to the air, water, and land, by updating the quantitative inventory at
least annually.
8. Ongoing dialogue with employees and members of the public
regarding waste and release information, progress in achieving reductions, and future plans. This dialogue should be at a personal, facc-to-facc level, where
possible, and should emphasize listening to others and discussing their concerns and ideas.
9. Inclusion of waste and release prevention objectives in research and in design of new or modified facilities, processes, and products.
ESW 108021 R. Page 35 of 98
WATER_PCB-SD0000021729
Pollution Prevention Code Pege 4
10. An ongoing program for promotion and support of waste and
release reduction by others, which may, for example,
include:
*
a.-----Sharing of technical information and experience with ------------ customers and suppliers;
b. - Support of efforts to develop improved waste and release reduction techniques;
c. Assisting in establishment of regional air monitoring networks;
d. Participation in efforts to develop consensus
approaches to the evaluation of environmental, health, and safety impacts of releases;
c.- Providing educational workshops and training materials;
f. Assisting local governments and others in establishment of waste reduction programs benefiting the general public.
11. Periodic evaluation of waste management practices associated with operations and equipment at each member company facility, taking-into account community concerns
and health, safety, and environmental impacts and implementation of ongoing improvements.
12. Implementation of a process for selecting, retaining, and reviewing contractors and toll manufacturers taking into account sound waste management practices that protect the environment and the health and safety of employees and the public.
13. Implementation, of engineering and operating controls at each member company facility to improve prevention of and
early detection of releases that may contaminate groundwater.
M. Implementation of an ongoing program for addressing past operating and waste management practices and for working with others to resolve identified problems at each active or inactive facility owned by a member company taking into
account community concerns and health, safety, and environmental impacts.
R. Page 36 of 98
DSW 106022
WATER_PCB-SD0000021730
Pollution Prevention Code . Page 5
Industry Trend Data To develop and maintain statistical industry trends. CMA will collect currently available data. Each company shall report annually to CMA. or -its designated agent, for each facility:
o Releases of substances as reported under SARA Section 313; and
o Wastes generated, as defined and reported in CMA's annual waste survey.
Member Self*Evaluation. Each member company shall report annually to CMA, or hs designated agent, the stage of implementation or each management practice in this Code. The reports shall be on the member self-evaluation form attached as Attachment A.
OSW 108023
R. Page 37 of 98
WATER_PCB-SD0000021731
Pollution Provontlon Code Page 6
Glossary of Terms
As used in this Code, key terms arc defined as set forth below. Note that these definitions may be broader than regulatory definitions, and that adherence to this Code does not relieve a company of the obligation to meet Federal, state and local regulatory requirements.
Facility - A she used for chemical manufacturing, processing, refining, packaging, R&D, distribution or related commercial activity.
Recycle A practice which regenerates or processes a material from a process to recover a useable product or material for reuse.
Release - Any emission, effluent, spill, discharge or disposal to the air. land, or water, of any pollutant or contaminant, whether routine or accidental, at or from a facility. The term does not include shipment or distribution of chemical product, nor release to the environment as part of normal and intended use of a product by the consumer.
Reuse A practice that reemploys a material from a process cither as an ingredient in a process to make a product, or as an effective substitute for a commercial product in a particular function or application.
Source Reduction - A practice that reduces the amount of any release or waste generated at the source, including closed loop recycle and reuse before exit from a process. The term includes, among other practices, equipment and technology modifications, process and procedures modifications, reformulation and redesign of products, substitution of raw materials, and improvements in housekeeping, maintenance, training and inventory control.
Treatment A practice, other than recycle or reuse, that alters the physical, chemical, or biological characteristics or the volume of a waste through a process or activity separate from the production of a commercial product or the provision of a service.
Waste - Any gas, liquid, or solid residual material at a facility, whether hazardous or non hazardous, that is not used further in the production of a commercial product or provision of a service and which itself is not a commercial product.
R. Page 38 of 98
OSH 108024
WATER PCB-SD0000021732
POLLUTION PREVENTION CODE
REPORT 1: MEMBER SELF-EVALUATION FORM FOR THE 1991 REPORTING YEAR
Instructions for the Company Responsible Carr* Coordinator 1. This form is to be submitted annually to CMA by each member company. This year the due date is XXX 31.
1992. Please submit directly to: 2. Indicate on page 1 the number of your member company's facilities that are subject to the Code. Each
company's Responsible Care* Coordinator must report the implementation stage for all facilities subject to the Pollution Prevention Code on this farm. 3. The Self Evaluation form for the 1991 reporting year covers fourteen management practices. DO NOT COMPLETE THIS FORM. JCMAwlH send the SelfEvaluation Form far the 1991 reportlngyearlnAprll/May 1992.] 4. For Management Practices 1*11 and 23 on the following pages, indicate the number of facilities that have attained each implementation category. Identify the current implementation category for each of your facilities at the timg you complete the form. Formanagementpractlccs 12 & 14. Indicate the company-wide reporting using a percentage (following instructions on page 5). 5. For the Industry Trend Data, show the total number offacilities in each appropriate box. The total number of facilities for each type of Trend Data should equal the total number of facilities subject to the Code. 6. Only subject facilities owned or operated as of the reporting date should be Included. 7. The implementation categories are: Category NA - No action. Ifno actiontakenbecause themanagement practice Isnot applicable, please explain. Category EV Evaluating existing company practices sgalnst the Management Practice. Category DP - Developing plan to implement Management Practice. Category 1A - Implementing action plan Category PP - Management Practice m place. Category R1 Reassessing Management Practice implementation. 8. Ifany facilities are shown m Category NA. please add anypertinent remarks tothe space marked "comments."
i08025
R. Pge 39 of 98
WATER_PCB-SD0000021733
POLLUTION PREVENTION CODE OF MANAGEMENT PRACTICES
REPORT 1: MEMBER SELF-EVALUATION FORM FOR THE 1991 REPORTING YEAR
i
Member Company Name:________________________ Responsible Care* Coordinator Name:__ Address;
Telephone: f 1 Number of facilities subject to the Pollution Prevention Code
R. Page 40 of 98
DSW 108026
WATER_PCB-SD0000021734
POLLUTION PREVENTION CODE
%
Industry Trend Data
V
Report annually to CMA or Its designated agent, the number of facilities for which annual report to CMA has or has not been submitted:
Annual Report Submitted"
T-l. Release of substances as re ported under SARA Sectlon313: and
T-2 Wastes generated, as defined and reported in CMA's annual waste survey.
Pons
R
J Form 1 JBL
1
1
Annual Report Rot Submitted*
Total FaellltlM
"Enter the number of facilities.
ROTES:
1. CMA expects to receive release data only from those facilities that are required to complete the Form R following the requirements in the Superfund Amendment and Reauthorlzatlon Act (SARA) Section 313 and EPA's clarifying regulations and Instructions.
2. Instruction: Under Form R. enter the number of facilities that are submitting TRI data to CMA
line T-l:
These facilities should submit the same data as EPA requires. The 313 Form R release data are due to EPA on Jufy 1.1992 and to CMA an July 31. 1992.
Under Form NR. enter the number of facilities that are not subject to the EPA reporting requirements. These facilities should complete Form NR Companies, not required to report 313 release data to EPA mav volunteer to send release data to CMA These facilities are not required to submit TRI release data to CMA as an obligation of membership.
line T-2:
The 1991 Reportingyear is the first year that facilities must complete CMA's annual Waste Survey as an obligation of membership under the Pollution Prevention Code.
0Sk IX)8027
R, Page 41 of 98
WATER_PCB-SD0000021735
Management Practice*
POLLUTION PREVENTION CODE OF MANAGEMENT PRACTICES
%.
Categoric* ^ ICA DP 1A Y? RT
1. A dear commitment by aenlor management through policy, communications, and resources, to ongoing reductions, at each of the company's facilities, in releases to the air. water, and land and in the generation of wastes.
Comments on Category XA:
2. A quantitative inventory at each facility of wastes generated and releases to the ah. water and land, measured or estimated at the point of generation or release.
Comments on Category XA:
3. Evaluation, sufficient to assist In establishing reduction priorities, of the potential impact of releases on the environ ment and the health and safety ofemployees and the public.
Comments on Category NA: _
4. Education of. and dialogue with, employees and members of the public about the inventory, impact evaluation, risks to the community.
Comments on Category KA*
Ctligiry KA Calagaiy TV CtUfry Or Catafary 1A
Category IT Ctnn7 XI
R. Page 42 of 98
I** ocUm. Vit tetlM taia iumi tha
ynctli*fa sat ayylli aM. yla*M aiplah.
rritutlaf ailattwg taspuy yrntlcM i|aiut Ui Mm|fi tiailln
DavalapUg ylaa U fanpUant Kut|at Prarttrt
layliaatlai ictla yia
Practice la ylu*. Xaaa--lng Kutfnaat Practice tatpl*maatatl*&.
OS* 108 026
WATER_PCB-SD0000021736
5. Establishment of priorities, goals and plans far waste and
release reduction,
into account both community
concerns and the potential health, safety, and environmental
impacts as determined tinder Practices 3 and 4.
JCuttfgrtct NA EV DP IA ------- 1-------- 1--~--i-----------,
RI --
6. Ongoing reduction ofwastes andreleases, giving preference first to source reduction, second to recycle/reuse, and third to treatment These techniques may be used separately or in combination with one another.
Comments on Category NA:
7. Measurement of progress at each facility In reducing the generation of wastes and in reducing releases to the air. water, and land, by updating the quantitative inventory at least annually.
Comments on Category NA:
& Ongoing dialogue with employees and members of the pubhc regarding waste and release infarmatlaa. progress In addevtqg reductions and futureplans. Thisdialogueshouldbeataperecnal lace-to-face level, where possible, and should cmphasfrg hateatng to others and discussing their ccnccna and ideas.
Comments on Category NA:
CtUgorp XA Ctgrr tV C*tt|n7 OF Ctli|7 1A Utt(7 FT
CaUfory Rl
X* ketln. B h ottoa taka hai tk Biat|not yractta to met ifjBrrtfi. plMM ayUa
trtiutlaf artattmi tcapuj pruticn afateit (k Uui|tsa ttailta
Dnttopiat ?l*a U ImpUam Kaufoaot Fnettoa.
lapliaatlag ottos pla
Masatmat Fracttca to pkc*.
KiumOaf toaaafinunt Fracttca taapWiawitirt--
S W 10 8) 2 9
R. Page 43 of 98
WATER_PCB-SD0000021737
Categories NA EV DP 1A PP
9. Inclusion of waste and release prevention objectives in research, and to design of new or modified facilities, pro cesses. and products.
pnmmfntu on Category NA.'_
RI
10. An ongoing program for promotion and support ofwaste and release reduction by others, whichmay, far example, include:
a. Sharing of technical information and experience with customers and suppliers; *
b. Support ofefforts to develop Improved waste and release reduction techniques:
c. Assisting m establishment of regional air monitoring networks.
d. Participationm efforts to develop consensusapproaches to the evaluation for environmental, health, and safety impacts of releases:
e. Providing educational workshops and tratamgmaterlals:
Assisting local governments and others m establishment of waste reduction programs benefltang the general public.
Comments on Category NA:,
11. Periodic evaluation of waste management practices associ ated with operations and equipment at each member com pany facility, taking into account community concerns and health, safety, and environmental bnpacts and implementa tion of ongoing improvements.
Comments on Category NA:
Cataf*ry M Clfa*y KV
CUf7 DP
C*tafry 1A
Calaforj TT
CU*forj at
Page 44 of 98
* Mtlm. * a* Mti tiAaa Vn Ui
putiM U mmi appgcSU. pUw*
Crtteattaf aMS| naapamj pnetUm ifilut Ui Mutimat hutt**.
X>rrtWrta( plaa t* faaptmaat KiM|WiMrt PtacttM.
ImplMMstiaf kUm piam
Uui|raat fncOci ta flact.
MMiita| Uiu(nai Practice tmtaaaatatlaa.
-,,
108030
WATER_PCB-SD0000021738
12. See Instructions below.
Categories NA EV DP LA pp
RI
13. Implementation of engineering and operating controls at each member company facility to Improve prevention and earty dfifvfrrn of releases that may contaminate groundwater.
Pnmmfnti on Category NA;
__
----- ------ -
*/ - - --
Instraction* for Practice* 12. Centractdr Review. and 14, PuLllfg
CMA recognizes that companies mayImplement Practice* 12 and 14 on a company-wide or even corporation-wide bun rather than on a facility basis. Therefore. CMA. asks companies to complete the Self-Evaluation Form using percentages that represent company-wide implementation for these two practices. In adding up the total percentages across all of the six categories. the number must equal 100%. Also, please use onlywhole numbers. Forthese two management practices the number offacilities used to calculate the percentage may exceed the number of facilities shown on page 1.
Companies may use ary appropriate method to rakuhte these parentages. One caudal companies wfll want to carefully consider lww this calculation is pefermed and uae It on a yearly basis so that the data from year to year can be compared meaningfully.
Categories
NA EV DP IA PP
12. lwpWnpntattnn ofa pffvyc
rwtnintng srvi TSyVmtrtg
contractors and toll manufacturers taking toto account sound
wastomanagancra practices thatproteathe environment and the health and safety cfemployes arid the pubhe.
Comments on Category NA:
Rl
14. hnplementationcfancngctngpropamiaraddresstngpastpperat* tng and waste managsnait practices and iar weridng wtth others to resolve identified problems at each active or tractive facHtty owned by a member company, taking into account curnmnfly concerns and health, safety, and envtranmaata] aspects.
Comments on Category NA:
C*ug7 M
Cstf*7 IT
cx*cT7 or
Califor? IA
CtlqarrlT Citfory U
-
-
Hi ictlis. Vsi aettas tafcis litisi tfci soa(iM( prmctlei U sit ifplukla. plaaai njilils
irUtlnf ttspu; putits iftlut tki Masafnaast Fractlaa.
DiTiUpUf pUa ti ImpUmcat Kaaafiaaat ersctlaa.
lapliaatlsf aetlas pin
Uu<|tBat hutlct Is pirn.
>iinitti| Masafitsasl Pnctlii bnplyranti--
DSW 106031
R. Page 45 of 98
WATER_PCB-SD0000021739
Pollution Provtntlon Cod* Page 7
ATTACHMENT C
- ..
WASTE ANO RELEASE REDUCTION
Xf.
. CODE OF MANAGEMENT PRACTICES QUESTIONS AND ANSWERS
1. Is this s voluntary or aandatory policy?
Aasvsr: Ths Vasts and Release Reduction Coda of Maaageaeat Praetlcss has boas developed radar CMA's Responsible Cara prograa. Adherence.to ths Saspossibls Cara (tiding principles is an obligation of oaabarship in CMA.
2. Mast ths Maaagaaaat Practicas ba eoaplatad ia tha spaeifie ordar listad?
Answer: Tbs Maaagaaaat Practicas ara laid oat ia a logically saqaaatlal pattern to eoaplata a xadactloa project. Tha sequence should ba generally adhered to although slight re-arrangeseat radar specific cireuastaaces nay ba warranted.
3. Since ths scope of this policy covers all hazardous and eoa-hazardous wastes aad releases, doesn't the Code require too aueh too fast or dilute the focus froa hazardous pollutants?
Answer: Tha pablle is not seeing or asking a distinction between hazardous and aon-hazardous releases aad wastea. Public opinion research shows that tha public wants releases lowered aad performance improved. This research indicates that the public is concerned about both cheaicals and trash generated by Industry.
The definition of "hazardous" is not unifora throughout the United States, since aany states have their own definitions that are aore restrictive than the federal ZPA'a. Furthermore, these definitions of "hazardous" keep changing over tiae.
Each coapany is starting froa differing points. Eaeh eoepaay oust identify its own reduction opportunities, identify the concerns of its own public, determine the reduction priorities and goals, and develop aad iapleaeat its own reduction plan. The goal of this Code is continued performance laproveneat by a long term coealtaent to the reduction of wastes and releases.
R. Page 46 of 98
QSW 108Q32
WATER PCB-SD0000021740
Pollution Prevention Code Page 8
4. Vby does thi* Code appear to endorse redactions for reductions sake? Vby should wastes and releases be reduced below health-based standards? Vhy should wastes and releases be reduced below levels allowed by statute, regulation, or pezait?
Answer: Tbs public does not endorse the concept of "permitted" generation of wastes or releases to the environaent. The public desires an increased aargin of safety and envlronaental protection as a goal. If the policy is to address the concerns of the public, it aust require sustained reductions.
5. Is this Code a-never-ending spiral of reduction?
Answer: The policy Is flexible so that eaeh coepany can assess the viability of further reductions. Certainly, reductions will be sustained under the Code as long as they are technically and econoalcally viable. To the extent reduction options reaaln viable, the goal is to establish a long-tern, substantial downward trend in wastes generated and releases to the environaent.
6. Will this Code cause neaher to accoapllsh substantive reduction?
Answer: To achieve the goal of earning the public's trust through laproved performance, real reductions oust occur. Therefore, this Code has aeasurable iaplenentatloa stages and industry trends data subaisslon requireaenta.
7. Does this Code apply to both large and snail conpanies and facilities? Is there a threshold below which this Code does not apply?
Answer: The Code applies to all aeabers of CHA. Even a saall coepany or facility can generate westes and releases to the environaent. There is no threshold for voluae of wastes generated, releases to the environaent, or sise of facility below which this Code does not apply. Each coapany/facility will establish its own priorities. The Code envisions progress by all of industry in reducing wastes and releases.
8. Does this Code apply to domestic or world-wide operations?
Answer: The principles behind the Code are universal in concept. The reduction of wastes and releases is good business and good eltixenship. However, for purposes of CHA eligibility requireaenta, the Code applies to that portion of a corporation or company that is used to determine Q1A dues.
DSW 108033
R, Page 47 of 98
WATER PCB-SD0000021741
Pollution Prevention Code Page 9
9. What-about multi-divisional eompasiea? Does this Cod* apply to mining operations? Service stations? Warehouses?
Answers: Adherence to the Code of Management Practices is a Guldins Principle of the Xesponsible Care program. The lesponslble.Care progras is a aemberahip requirement for those ___portions of a eoapany that determine the CKA dues structure. The principle of reducing wastes and releases la responsible corporate behavior and should be encouraged throughout as organisation.
The Waste and telease Induction Code of Management Practice is designed for flexible implementation by companies and facilities. Each company/facility must determine the reduction opportunities, priorities, baseline, and implement the reduction plan is accordance with these company/facility-derived goals. Inherent in this Code is the need to communicate with the-public when determining reduction opportunities and priorities. Therefore, while the seope of this policy is broad, each company must identify the sources that are included in its implementation activities as well as the priority and timing for these reduction activities.
10. If all of the chemleal industry is to be affected, how do we ensure fair and equitable reductions? Bow do we prevent competitive disadvantages among CMA member companies?
Answer: The Waste and Kelease Induction Code is predicated on making reductions that are economically and technically sound. The Code does not envision enforcing competitive disadvantages on eesber eoapanles by usurping their decision''making processes. Each company oust evaluate its own reduction opportunities and develop its own reduction plan to meet company/facility priorities.
11. If all of the chemleal industry is to be affected, how do we ensure fair and equitable reductions? low do we prevent coapetitive disadvantages with ether industry segments?
Answer: This Code will actually make our industry more coepetltlve than those that do not embrace its concepts. Waste and release reductions will result in less wastes, improved efficiency, and make the industry a superior competitor.
12. Is this a son-growth Code? How can this Code be reconciled with the seed for expansions? Bow are opportunities for emission offsets (seeded for sir permitting) to be preserved?
Answer: This Code envisions a long-term, substantial downward trend is total releases to the environment and waste generation. However, the method of achieving reductions is left to the needs and priority determinations of the individual member companies.
R. Page 45 of 98
DSW 108034
WATER_PCB-SD0000021742
Pollution Prevention Code Page 10
The policy la not a no-growth policy; rather, it la a policy of balancing future expansions with future waste and release reductions.
Voluntary waste and release reductions eay be eligible to be banked with appropriate governeental agencies. Any plan for waste ........... -and release .reductions,oust also plan to aecoeaodate expansions. Public perceptions say ultlaately require a waste and release reduction type prograe just as a condition to be able to construct or expand. Several states already have proposed such regulations.
13. Won't this Code have enornous eeonoeic consequences?
Answer: Waste ani release reductions nay or nay not have a huge price tag. Sons reduction projects* like fugitive eaission sbateaent, tend to pay for tbaaselves in recovered product(s); other projects nay increase the price of doing business. Industry cost be willing to Invest in plants that will lead to a future with less wastes and fewer releases to the envlronsent. The goal of Responsible Care is that the cheaical Industry will leprove the perforeance of its operations constantly.
In eaking reduction progress* each eoapany oust look at all the reduction opportunities and set their own priorities. Each eoapany can set the scope of these priorities broadly or narrowly and iapleaent actions at their own paee.
Each eoapany Bust identify its own reduction priorities and iapleaent a reduction plan to aeet eoapany/facility-set goals.
11. Does the hierarchy of reduction aethodologles aesn that all projects aust use source reduction unless it is technically Infeasible?
Answer: Each waste and release source aust be evaluated for its reduction potential. The hierarchy requires that reduction projects for source reduction be evaluated before reeycle/reose or treataent. however, the project to be lapleaented will depend on the evaluation.
Technical lnfeeslblllty is only one of several facility and/or waste specific criteria that can lead to selection of a reduction project involving reeycle/reose or treataent. When developing their reduction priorities, coapanles aay choose to consider other criteria including risk/benefit aechanisas, public concern, sire of the feellity, econoalce, and other feetora such as conservation of resources.
1-08035
R. Page 49 o(98
WATER_PCB-SD0000021743
Pollution Prevention Code Pege 11
15. This Code, as well as other codes under the Responsible Cere profree, require ongoing dialogues with eaployees and aeebers of the public. Does eaeh such Manageaent Practices require a separate aeetlngT
_ ..Answer: Mo. Meetings with eaployees or the public can have aultiple agenda itaas. If several Manageaent Practices iteas are to be covered in a single nesting, all that is required is that the agenda and presentation clearly address eaeb topic, rather than have a general "discussion of topics."
Under the Responsible Care Prograa, the process to eoaaunicate with the public and eaployees is established under the Coaaunlty Awareness and Eaergeney Response (CAES) Code of Manageaent Practice. Coapanles are encouraged to use the aeehanisas set up under other codes to enhance effective iapleaantatian of the Responsible Care Prograa and to better use and conserve eoapany resources.
16. Is dialogue with the public required for all facilities?
Answer: Meaningful dialogue is essential to better understanding public concern, laproving the public's understanding of our operations, and building trust. Soee facilities, due to sise and location, nay have Halted opportunity for sueh dialogue. Where the opportunity for dialogue exists, even on a Halted basis, it should be actively pursued individually or' jointly with other neighboring coapanles/fseilltles.
17. Should individual coapanles and/or facilities subalt to CMA the rationale behind the annual Industry Tread data subaisslons?
Answer: No. The data subeitted for the Industry Trend Data reports need not have supporting doeunentatlaa subultted to CMA. However, when discussing these data with the local public, it is assuaed that general aetbods and assuaptlons will be discussed as part of the public education and dialogue process.
18. When eoapletlag the Self-Evaluation Porn, wust every facility atteapt to progress through all the lapleeentation stages, or can soee facilities "nature" their progress in code lepleaentation at less than full lapleaentatlan?
Answer: All participating facilities should work to achieve full lapleaentatlan of each Code and eabrace the concepts of this Code in the spirit of the Responsible Care Guiding Principles. Depending on the sire of particular facility or the activities carried on by that facility, a eoapany aay decide that different lepleaentation aethods are appropriate, for exaaple, a large facility aay use foraal procedures such as written policies and
R. Page 50 of 98
OSW 108036
WATER_PCB-SD0000021744
Pollution Prevention Code Page 12
annuals and conduct foraal ploy** tings. Vharaas, a sallr facility can accomplish th aaaa lap]antation using lass foraal tbods.
SM 108037 R, Page 51 of 98
WATER_PCB-SD0000021745
Pollution Prevention Code Page 13
Attaehaent B
QUESTION AND ANSWERS FOR PRACTICES 11-14
Thaae questions address Issues la the four practices added to the Pollution Prevention Code of Manageaent Praetlees. As coapanies lspleaent Praetlees 1-10, they should examine their lapleaentation actions and Modify then to include waste Manageaent.
QUESTIONS:
IN PRACTICE 11. WHAT ARE THE WASTE MANAGEMENT PRACTICES ASSOCIATED WITH ALL OPERATIONS AND EQUIPMENT?
The Code envisions coapaales reviewing all waste aanageaent practices at eaeh step of the operations) where wastes are generated or released within eaeh facility. This review is within the operating processes not Just at the "end of the pipe."
WHAT DO YOU MEAN BY A CONTRACTOR AND TOLL MANUFACTURER?
Contractors are any entity a aenber coapany uses to handle its secondary Materials and wastes. This Includes, for axaaple, waste treateent facilities, disposal facilities, tank cleaners, redaiaers, recyclers, and the like. "Contractors" does not include publicly owned treataent works.
Responsible Care# covers toll Manufacturers * operations under two Codes. This code covers the wastes generated by relevant operations of toll Manufacturers. For the purpose of this eode, toll Manufacturers are independent parties who: perfora a Manufacturing step for a aenber coapany in which the aenber eoapany owns the work in process; use the neaber coapany's feed stock; and generate waste froa the Manufacturing step.
R. Pape 52 of 98
DSW 108038
WATER PCB-SD0000021746
ro i w w w* ri r f c < w<t wUUC Page 14
WHAT DOES "IHPLEMDJTATION OF A PROCESS. ..." MEAN?
The requirement for tbe "Implementation of a process. . .."la designed to encourage member companies to do business with those contractor* and toll manufacturers that, after raaaonabl* inquiry, are believed to u|a|* in sound vast* management practices.
As part of tba contracting procedure, saabar cospanias should consider including language requiring tba contractor to usa propar health, safety, and onTiroosental practice* and stating that tba saabar coapany has a right to inspect for that purpose.
HOW DO YOU REVIEW THAT A CONTRACTOR OR TOLL MANUFACTURER USES SOUND WASTE MANAGEMENT PRACTICES?
A process for "reviewing" includes reasonable reviews of tbe relevant practices of contractors and toll manufacturers. Because of tba variety of.conaerclal relationships and circumstances, seaber cospanias are to exercise their own judgement as to how to conduct "reviews" and precisely what to do with tbe information obtained.
CHA nsabers are sot expected to control tbe operations of their contractors and toll aanufaeturers. CMA aaaber eospanles should consider perforslng a site visit and visual inspection of waste sanagesent practices by a company representative. Tbe seaber cospany say determine that a sore rigorous inspection is appropriate based on initial findings.
HOW OFTEN SHOULD YOU REVIEW CONTRACTORS AND TOLL MANUFACTURERS?
A review or evaluation should be done on some repeat basis. Companies should determine tbe tlalng by an evaluation of tbe results of previous reviews, potential impacts, potential liability, etc.
WHAT DO VE KEAN BY "IMPROVE THE PREVENTION OF RELEASES TO GROUNDWATER?"
The goal is to prevent releases to tbe ground and to protect existing groundwater quality. While it is envisioned that a company will have an SFCC (Spill Prevention Control and Counterseasures) plan for certain materials, companies should review the ebeaieals at tbe facility and extend tbe SPCC concepts to other materials. To improve efforts to prevent releases, member companies should review tbe ebeaieals and operations at a facility; develop plans to prevent, detect, and contain releases or potential releases; and iapleaent these plans to protect groundwater froa contamination.
0sw 1DB03S
R. Pape 53 of 98
WATER_PCB-SD0000021747
Pollution Prevention Code Page 15
IN PRACTICE 14 VHAT IS MEANT BY IMPLEMENTATION OF AN ONGOING PROGRAM TO RESOLVE IDENTIFIED PROBLEMS?
"laplemeatetioa of an ongoing program..." niu developing processes for eralusting the health, safety, and enrironBeatal inpacts of Identified problems arising froe peat operating end waste management practices end for setting priorities for addressing those probleas. The Code recognizes that not erery identified prohlea poses adverse impacts. Resolving identified problees should consider factors such as, regulatory, technical, and eeonoeie considerations.
WHAT IS MEANT BY "PAST OPERATING AND WASTE MANAGEMENT PRACTICES?"
Past operating practices and waste aanageaent practices that coapanles should consider nay include operating practices such as: aanufseturing operations, loading and unloading areas, storage, areas of spill containaent, and recycling and reuse processes; and waste aanageaent practices such as: surfsee iapoundaents, waste treataent, land disposal, land treataent and farming, and deepwell injection.
WHAT IS MEANT BY "WORKING WITH OTHERS TO RESOLVE IDENTIFIED PROBLEMS?"
Each aeaber company's program should include a process to cooperate, to the extent appropriate, with governmental agencies, past owners, operators, insurance carriers, the comvanity, and others to resolve the potential health, safety, and enrironaental impacts, and community concerns associated with identified probleas.
WHICH MEMBER COMPANY FACILITIES, ACTIVE OR INACTIVE, ARE INCLUDED IN PRACTICE 14?
This praetiee applies to facilities currently owned by a aeaber company. This includes properties that are still owned, but no longer have ongoing operations. Inactive sites that are not owned by a aeaber company, hut where the company has potential involveaent, should be eddressed to the extent the aeaber company determines feasible.
R. Page 54 of 98
DSW 108040
WATER PCB-SD0000021748
Pollution Prevention Code Page 16
WHAT IS MEANT BY "TAKING INTO ACCOUNT COMMUNITY CONCERNS AND HEALTH, SAFETY, AND ENVIRONMENTAL IMPACTS?"
When CMA ber coapaaies implement the employee aad public outreach of the Code (Practices 4 aad 8), companies should present laforaation about their carreat aad past vasts aaaageaent practices with the goal of identifying the coastmlty concerns. Companies should consider this laput when developing plans and setting priorities for waste aanageaent aad reaedlatioa activities.
DSW 108041 R. Page 55 of 98
WATER_PCB-SD0000021749
Page 56 of 98
DSW 108042
WATER PCB-SD0000021750
Responsible Care: A Public Commitment
PROCESS SAFETY CODE OF MANAGEMENT PRACTICES
Purpose
The Process Safety Code is designed to prevent fires, explosions and accidental chemical releases. The Code is comprised of a series of management practices that reflect this goal, with the expectation of continuous performance improvement for each management practice. The practices are based on the principle that facilities will be safe if they are designed according to sound engineering practices, built, operated and maintained properly and periodically reviewed for conformance.
Process safety is an interdisciplinary effort. Consequently, the Code is divided into the following four elements: management leadership, technology, facilities and personnel. Each element is composed of Management Practices. Individually, each Practice describes an activity or approach important to preventing fires, explosions and accidental chemical releases. Collectively, the Practices encompass process safety from the design stage through operation, maintenance and training. The scope of this Code includes manufacturing, processing, handling and on-site storage of chemicals. This Code must be implemented with full recognition of the community's interest, expectations and participation in achieving safe operations.
The process safety management program in each facility is complemented by workplace health and safety programs, as well as waste and release reduction programs which address and minimise releases and waste generatioa These three programs, and others, will help assure that CMA member facilities are operated in a manner that protects the environment and the health and safety of personnel and the public.
Relationship to Guiding Printiolg
The Code helps achieve several of the Responsible Care Guiding Principles:
To recognize and respond to community concerns about chemicals and our operations,
To make health, safety and environmental considerations a priority in our planning for all existing and new plants and processes.
To operate our plants and processes in a manner that protects the environment and the health and safety of our employees and the public.
DSW 108CH3
R. Page SI of 8
WATER_PCB-SD0000021751
Process Safety Code of Management Practices September 11. 1990 -- Page 2
Management Practices Each member company shall have an ongoing process safety program that includes:
Management Leadership . 1. Leadership by senior management through policy, participation, communications and resource commit
ments in achieving continuous improvement of performance.
.i
2. Clear accountability for performance against specific goals for continuous improvement.
3. Measurement of performance, audita far compliance and implementation of corrective actions.
4. Investigation, reporting, appropriate corrective action and foDow-up ofeach incident that results or could have resulted in a fire, explosion or accidental chemical release.
5. Sharing ofrelevant safety knowledge and lessons learned from such incidents with industry, government and the community.
6. Use of the Community Awareness and Emergency Response (CAER) process to assure public comments and concerns are considered in design and implementation of the facility's process safety systems.
Technology
7. Current, complete documentation ofprocess design and operating parameters and procedures.
8. Current, complete documentation of information relating to the hazards of materials and process technology.
9. Periodic assessment and documentation of process hazards, and implementation of actions to minimize risks associated with chemical operations, including the possibility ofhuman error.
10. Management ofchanges to chemical operations to maintain or enhance the safety originally designed into the facility.
Facilities
11. Consideration and mitigation ofthe potential safety effects ofexpansions, modifications and new sites on the community, environment, and employees.
12. Facility design, construction and maintenance using sound engineering practices consistent with recognized codes and standards.
13. Safety reviews on all new and modified facilities during design and prior to start-up.
14. Documented maintenance and inspection programs that ensure facility integrity.
R. Pace 58 ot 98
OSW 108044
WATER_PCB-SD0000021752
Process Safety Code ot Management Practices
September 11. 1990 -* Page 3
.
15. Sufficient layers of protection through technology, facilities and employees to prevent escalation from a single failure to a catastrophic event.
16. Provision for control ofprocesses and equipment during emergencies resultingfrom natural events, utility disruptions and other external conditions.
Personnel
17. Identification of the skills and knowledge necessary to perform each job.
18. Establishment of procedures and work practices for safe operating and maintenance activities.
19. Training for all employees to reach and maintain proficiency in safe work practices and the skills and knowledge necessary to perform their job.
20. Demonstrations and documentation of skill proficiency prior to assignment to independent work, and periodically thereafter.
21. Programs designed to assure that employees in safety criticaljobs are fit for duty and are not compromised by externa] influences, including alcohol and drug abuse.
22. Provisions that contractors either have programs for their own employees consistent with applicable sections of this Code or he included in the member company's program, or some combination of the two.
filraarv
This Code uses key terms in a context that may be broader than their associated regulatory definitions. However, adherence to this Code does not relieve a company of the obligation to meet Federal, state and local regulatory requirements.
Process Safety The application of management and engineering principles to prevent fires, explosions and accidental chemical releases at chemical process facilities.
Sound Engineering Practice The application ofmandatory codes and standards supplemented by the use of voluntary codes, standards and guidelines, tempered by professional judgement
Safety Critical Jobs. Jobs, activities and tasks, ifimproperly performed, that have the potential to significantly increase the risk of a fire, explosion or accidental chemical release.
Accidental Chemical Release - Unplanned, sudden releases of chemicals from manufacturing, processing, handling and on-site storage facilities to the air, water or land. It does not include permitted or other releases.
C5w IO8O45
R. Page 59 of 98
WATER_PCB-SD0000021753
R. Page 60 of 98
OSH 1080**6
WATER PCB-SD0000021754
SAMPLE
Responsible Care: A Public Commitment
i
CHEMICAL MANUFACTURERS ASSOCIATION MEMBER SELF-EVALUATION FORM
PROCESS SAFETY CODE OF MANAGEMENT PRACTICES
Member Company Name:
Responsible Care Coordinator
Name' Address:
...... -
Telephone ( ) Number of facilities subject to code
DSW 108047
R, Page 61 of 98
WATER_PCB-SD0000021755
R. Page 62 of 98
DSta 108(148
WATER PCB-SD0000021756
SAMPLE
PROCESS SAFETY CODE OF MANAGEMENT PRACTICES
Instructions:
1. Under the Responsible Care Initiative, each member company will submit a Self-Evaluation form annually to CMA.
2. Indicate on the cover page the number ofmember company facilities subject to the Code. Each company must report the implementation category for all facilities subject to the Code on this form.
3. For each Management Practice on the foDowing four pages, indicate the number of facilities that have attained each implementation category. Each facility should appear in only one milestone category per Management Practice. The total number of facilities subject to the Code should equal the number of facilities across all six implementation categories for each Management Practice.
4. Only subject facilities owned or operated as of the reporting date should be included.
5. The implementation categories are:
Category NA Category EV Category DP
Category IA Category PP * Category R1
No action. Ifno action taken because the management practice is not applicable, please explain. Evaluating axisting company practices against the Management Practice. Developing plan to implement Management Practice. Implementing action plan Management Practice in place. Reassessing Management Practice implementation.
lOQQt' g R. Page 63 of 98
WATER_PCB-SD0000021757
R. Page 64 of 98
S* ^08050
WATER PCB-SD0000021758
Process Safety Code ol Management practices November 21. 1991 -- Page 3
Management Practices
Categoric
Management Leadership
NA EV DP IA PP RI
1. Leadership by senior management through policy, participa tion, communications and resource commitments in achieving continuous improvement of performance.
Comments on Category NA:___________ ___________________
2. Clear accountability for performance against specific goals for continuous improvement
Comments on Category NA:
3. Measurement of performance, audits for compliance and im plementation of corrective actions.
Comments on Category NA:
4. Investigation, reporting, appropriate corrective aetion and fol low-up of each incident that results or could have resulted in a fire, explosion or accidental chemical release.
Comments on Category NA:
5. Sharing of relevant safety knowledge and lessons learned from such incidents with industry, government and the community.
Comments on Category NA:
CiUfr KA Catafary CV
Ciinorr DP C*Ufr XA Calagar7 W Catayor7 K1
Ha uSm. Vaa aetlaa uka licwi tki aaufaaM yractlea la aat ippBtalU, ylaaaa axplaia-
t?ihitla( (riitbi company practice* agalaat tka Maaafaaaat Practlaa.
'
Davaleptag plaa ta hnylwnant Kaaagaaaat Practlaa.
Implracattag actlaa fin
SUaafcsaat Practice la pleea
..............ttii| Ku*|<aat Practice tmpleaaat/***^.
DSw U18054
R. Page 65 of 98
WATER PCB-SD0000021759
Process Safety Code of Management Practice* November 21. 1091 -- Page 4
SAMPLE
CstfnrwK NA EV DP 1A PP HI
6. Use of the Community Awareness and Emergency Response (CAER) process to assure public comments and concerns are considered in design and implementation ofthe facility's process safety systems.
Comments on Category NA:--------------------------------- ------------ -
Technology
.
7. Current, complete documentation ofprocess design and operat ing parameters and procedures.
Pomment* on Category NA:
8. Current, complete documentation ofinformation relating to the hazards of materials and process technology.
Comments on Catenrv NA:
9. Periodic assessment and documentation ofprocess hazards, and implementation of actions to minimize risks associated with chemical operations, including the possibility ofhuman error.
Comments on Cateeorv NA:
10. Management of changes to cbemieal operations to maintain or enhance the safety originally designed into the facility.
Comments on Cateeorv NA:
CtU|7 IU Category EV Cfgry DP Calagurp 1A Catagory IT Cat agorj Ml
Page 66 of 98
Ka aedaa. V a* acdaa takaa tacaaai tha unagainanl pnctlet la mat appBcabla, plaaaa arpUtn. Evaluating aalatlag eampaay pnctkN agalast tha u***|l" ' hudet. Davaloptag plan ts baploant Maaagaaaat PnctUa. baplcmaatbig actlaa plan Maaagaaaat Practlea la ptotra !>--tng Maaagaaaat Practlea Implaaaatatlaa.
DSW 108052
WATER PCB-SD0000021760
Process Safety Code of Management Practices November 21. 1001 -- Page 5
SAMPLE
Categories
Facilities
NA EV DP IA PP RI
11. Consideration and mitigation of the potential safety effects of expansions, modifications and new sites on the community,
environment, and employees.
Comments on Category NA:____________________________ _
12. Facility design, construction and maintenance using sound
engineering practices consistent with recognized codes and
standards.
'
Comments on Category NA:
13. Safety reviews on all new and modified facilities during design and prior to start-up.
Comments on Category NA:_____________
14. Documented maintenance and inspection programs that en sure facility integrity.
Comments on Category NA:
15. Sufficient layers ofprotection through technology, facilities and employees to prevent escalation from a single failure to a cata strophic event
Comments on Category NA:
KA
Category EV
Cetognry M*
Category U
Category I?
Category Ml
He ictln. V ae ectiea tefcrn Wceeoe tke maaagaaaat practice U set typSetible, pleaae eeplatn, Bvsteatiag oSctiag ceayny prmcticae egeiaet tke Masegemoot frutke. Poroloptag ploa to tcopSeatoat Maaagoiaoot Practiac. ftnplewioetlaf iftlw ylw Xua|>Bat Practice ta place, aeeeeeering Maaegomoat Practice ImpleniMfflea
XSW 108053
R. Page 67 of 98
WATER_PCB-SD0000021761
Process Safety Code of Management Practice* November 21. 1991 Page 6
SAMPLE
Caicgorin NA EV DP IA PP RI
16. Provision for control of processes and equipment during emer gencies resulting from natural events, utility disruptions and other external conditions.'
Comments on Category NA:
Personnel
17. Identification of the skills and knowledge necessary to perform each job.
Comments on Category NA:
18. Establishment ofprocedures and work practices for safe operat ing and maintenance activities.
Comments on Category NA:
19. Training for all employees to reach and maintain proficiency in safe work practices and the skills and knowledge necessary to perform their job.
Comments on Category NA:
20. Demonstrations and documentation of skill proficiency prior to assignment to independent work, and periodically thereafter.
Comments on Category NA:
cuer
Category EV
CatagerfDP Calagar? IA
Category
Category U
* aetia*. Va* actlaa Ukaa liareaei tka HM|iant gcactlca U Mt ppBeitk |I*m explain. Sraloatlae adatlag ompmaj pvectlcaa agateat tka lfai|BMl Prectlaa.
Peealoptag plaa ta teplamaat Maaagamaet ftartlM buplcmcatlag actlaa plaa Management prmctica la plana
Pemaoetng Memgeaiaal Practice fanplaMtatlaa.
^0805*t
Pape 68 of 98
WATER PCB-SD0000021762
Process Safety Code of Management Practices
November 21. 1991 - Page 7
`
SAMPLE
NA EV DP IA PP RI
2L Programs designed to assure that employees is safety critical jobs are fit for duty and are not compromised by external influences, including alcohol and drug abuse.
Comments on Cate?orv NA:
i
22. Provisions that contractors either have programs for their own employees consistent with applicable sections ofthis Code or be included in the member company's program, or some combina tion of the two.
Comments on Caterorv NA:
CU|or7 KA Catagary CV Catagary DP Catagary 1A Catagary PT Caiagoiy XI
Xa aetlaa. V aa action takas kacaaaa tka maaagaaaat practlca la sat cppBcabla, plaaaa aiplata, Datuttai arlittng company pnctlcaa agaiaat tba Kau|aust Practlca. DeraWplag plaa ta tmplamast Kasagamaat Practlca. Implamawftiig aetlaa plaa Rasagamaat Practlca Is plaaa. Waaaaaaahtg Masagwnaat Practlca 1 aipl am oaTitian
OSW 108055
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WATER PCB-SD0000021763
R. Page 70 * 98
OS* 108056
WATER PCB-SD0000021764
Process Safety Code of Management Practices Questions and Answers
Management Leadership
1. Q: How does one define senior management?
A: Senior management is that level that has the authority to establish policies and authorize expenditures to implement them. As used in this Code, this probably includes plant managers and above.
2. Q: What is meant by participation by senior management?
A: Participation in this context refers to activities which convey and reinforce commitment and leadership as well as support the implementation of policies and procedures.
3. Q: Is it necessary to have a written process safety policy?
A: Yes.
4. Q: What parameters can be used to measure process safety performance?
A: Each company should establish its own methods of measurement. Counts of unwanted incidents, frequency rates, property loss statistics, audit violations, permit violations, risk reviews and completion of training are a few examples.
5. Q: How should one define the type ofincident that should be investigated?
A: There is no single standard which defines the type of incident or near-miss to investigate. Management should establish a formal procedure to investigate those uncontrolled events which have potentially serious consequences.
6. Q: Whet should be done after each incident or near-mias investigation?
A: Corrective actions or follow-up should be identified, earned out and communicated as appropri ate within the company.
7. Q: What kind of knowledge and lessons should be shared?
A: Knowledge and lessons which can benefit othersbecause oftheirgeneral applicability or novelty or unusualness. Member companies may establish procedures to promote sharing consistent with proprietary and legal considerations.
108057
R. Page 71 of 98
WATER PCB-SD0000021765
Process Safety Code of Management Practice* September 11. 1990 -- Page 2
S. Q: How much input do you envision our industry receiving from the public sector?
A: The CMA fully supports the concept* ofworking with local communities to listen to their view* and concerns and to consider them in plant safety systems. The intent is to discuss major process additions and new grass-roots construction as opposed to minor plant changes. Individual companies are responsible for the safe design and operation of facilities; that responsibility cannot be shared with the public. Itis intended that public concerns be considered in design and operations of the facility. The CAER network provides a useful vehicle to accomplish this.
Trchnolflgy
9. Q: What type of documentation of process design and operating parameter* should exist?
A Each operating unit should have up-to-date safety related information that contains the design basis and procedures, (e.g., process flowsheets, piping and instrument diagrams or engineering flow diagrams, vessel drawings, electrical area dasaifieations, safetyvalve capacity information and operating manuals). The documents will serve as the bade bone for employee training, hazard evaluation and process modifications.
10. Q: What is meant by operating parameters?
A Operating parameters are the ranges of conditions (eg. temperature, pressure and flow composition) within which a unit is designed to operate. Within that range, a unit is expected to operate without any problems. For example, the safe operating parameter for a reactor temperature during exotherm might be 70 degrees minimum to 130 degrees maximum. Operating outside the range could cause instability in the reaction -- runaway temperature if above, potential brittle fracture if below.
11. Q: What are some ofthe types of information needed to define the chemistry?
A Each reactant and product should have a material safety data sheet (MSDS). Chemical reaction kinetics and acute toxicity should be known and understood. Reactive chemical performance upon mixing various chemicals in different proportions should be documented. Waste streams should be included as well as reactants and products.
12.Q: What type of procedures should be maintained?
A Generally, all routine jobs or tasks with process safety implications should have written stepby-step instructions. These procedures should capture the experience base ofthe knowledgeabl e experts. The protective equipment and employee concerns should be incorporated in the procedures. Also, emergency procedures must be clear and unequivocal
13. Q: What is the difference between documentation covered in practice 7 versus that included in practice 8?
A Number 7 refers mainly to design and operating information, while number 8 specifically addresses the hazards associated with the unit being evaluated.
Ptfe 72 of 98
OSH 108058
WATER_PCB-SD0000021766
Process Safety Code of Management Practices September 1 i. 1990 -- Page 3
14. Q: Doe* the reference in the Code to risk imply that we will be required to perform quantitative risk assessments on all our plants?
A: No. Qualitative analysis alone should be sufficient to satisfy process safety analysis objectives in most eases. In any ease, qualitative analysis should be considered prior to performing numerics! frequency or consequence calculations.
15. Q: What does periodic assessment of process hazards mean in the technology element?
i
A: Each member company should establish its own review frequency based on inherent hazards, operating experience, rate of technology change and other factors. Typical review frequencies range from three to seven yean. Under very special circumstances, review frequency may be as short as one year.
16. Q: What is meant by `management of change"?
A: "Management ofchange" means having management systems in place that ensure the original safe design of the mA is maintained and all changes, including minor modifications, are properly reviewed, recorded and communicated.
17. Q: What changes should be covered?
A: All changes except like for like substitutions. Examples include hardware, procedures, raw materials, operating conditions, throughput, employee, software and control mode.
18. Q: There does not seem tobe a dear distinction between Technology andFacilities - shouldn't these two sections be combined?
A: While it is true that the two sections are closely related and interdependent. Technology (Le.,
chemistry and know-how) and Facilities (Le., equipment and hardware) each deserve an
independent focus as related to process safety.
.
Fadlitici
19. Q: Should the community be consulted when considering potential effects of a new site or new
installation?
A: Yes, using principles of the CAER process.
20. Q: Does this mean the community has approval or rejection authority over our projects?
A: No: It means that we should identify and respond to community concerns.
DSW L0805-9
R, Page 73 of 98
WATER_PCB-SD0000021767
ProceM Safety Code of Management Practice*
September 11. 1990 -- Page 4
.
21.Q: Choosing a new plant cite involves many complex considerations. Can we realistically expea to completely satisfy all interests?
A: Possibly not, but the Responsible Care Guiding Principles require health, safety and the environment to be priority considerations and such issues must be adequately resolved.
22.Q: Does the Code cover concerns about sabotage or terrorism?
A Such issues are notintended to be within the scope ofthe Code. However, good practice in site
selection and planning will consider such general security issues as buffer zones, fencing,
lighting, entrance gates and security surveillance. Also, mitigation and emergency response
measures can help
consequences ofhostile sets.
23. Q: Does "sound engineering practice" extend beyond mandatory codes and regulations?
A In many eases, yes. While government codes and regulations may establish minimum legal requirements for plant design, operation and maintenance, member companies are expected to use qualified professionals to identify and apply other engineeringpractices (such as contained in many non-mandatory or consensus standards or codes) as may be necessary to fulfill our safety commitment to employees and the community.
24. Q: Are "Safety Reviews" as prescribed in practice 13 different from "Process Hazard Assessments" as prescribed in practice 9?
A Yes. "Process Hazard Assessment* is done during the process design stage and periodically thereafter. It focuses on the hazards inherent to the process and measures to control these hazards. "Safety Reviews" use "Process Hazard Assessment" as a starting point and focus on the physical installation to assure that it is in accordance with design and is safe to start-up and operate.
25. Q: Shouldn't Safety Reviews go beyond simple field inspection?
A Yes. Safety Reviews may include such things as testing equipment, controls, control logic, interlocks, "water runs" etc., prior to operation with hazardous materials. In addition, such reviews should also confirm that process documentation and procedures are in place and that operators have been trained.
26. Q: Doesn't a "Preventive Maintenance Program" meet the requirement of practice 14?
A To meet the intent of this code practice, the preventive maintenance (PM) program must go beyond operating reliability and economic considerations and address all potential failures which, while possibly extremely unlikely, could impart process safety. A program to "ensure facility integrity" must search outbidden deterioration and flaws that can result in sudden and unexpected failure that can impact process safety.
Page 74 of 98
108060
WATER_PCB-SD0000021768
September 11. 1990 -- Page 5
27. Q: What are some examples that could be included in a PM program to satisfy practice 14''
A Metallurgical examinations for stress corrosion cracking, nondestructive acoustic testing, compressor vibration monitoring, thickness measuring for erosion or corrosion on key parts of pressure vessels and pipelines, verification of bolt and damp material of construction and quality, reliability of critical instruments and operation of safety valves are examples.
28. Q: Shouldn't a hierarchy be considered in applying "layers of protection"?
A Normally technology should be applied first, choosing an inherently safe or less hazardous process wheneverpossible. Then hardware, safetyfactors,redundantcontrols, failure detection systems, etc., should be applied. Finally, emergency procedures and employee training should complement the process and hardware design.
29. Q: How many layers constitute `sufficient layers of protection"?
A There is no absolute answer to this question. The number of levels needed depends on the
likelihood ofan
failure, the nature ofthe consequences and whether additional levels of
protection will materially improve safety. Layers of protection include more than redundant
equipment. They may include process techniques, instrumentation and hardware, operating
procedures and operator training.
30. Q: What is meant by "external conditions"?
A By external conditions we mean anythingthat is beyond the direct and immediate control ofthe process operator. An example might be an evacuation order for your plant caused by a fire or toxic release from a neighboring plant as well as an upset or incident in an adjoining process unit
Pcrannacl
31. Q: We train our employees thoroughly, why is it necessary to also demonstrate their proficiency?
A: Even with the best employee trainingprograms, people learn at different rates and comprehen sion. An actual demonstration is the only way ofbeing sure that each individual has grasped essentia] concepts or skills. Demonstrations can involve written tests and/or having the trainee show a qualified observer how they would do a job.
32. Q: Do procedures and work practices have to be documented?
A: Generally, yes. Procedures typically require proper execution of several stages. Documented procedures help assure that a critical action is not overlooked and that the procedure is carried out consistently by everyone.
33. Q: Does the code require that employees be screened for alcohol drug abuse?
A: No. The Code requires programs designed to assure fitness for duty.
-DSW 108061
R. Pge 75 of 98
WATER PCB-SD0000021769
Ptocbm Safety Code or Management Practices September 11. 1990 -- Page 6
34. Q: What kinds ofjobs are safety-critical?
A: A position is safety-critical when it involves tasks which, if not performed proDerly, can significantly increase the likelihood of a fire, explosion, or accidental chemical release.
35. Q: What is meant hy "external influence"?
A: External
include abuse of alcohol or drugs, but the terms also refers to any factor
which might impairjudgement, attention or general capacity to perform ajob safely. Examples
include physical impairment, emotional stress, and stress from too much overtime work.
R. Page 76 of 98
OSH 106062
WATER_PCB-SD0000021770
Responsible Care: A Public Commitment
EMPLOYEE HEALTH AND SAFETY CODE OF MANAGEMENT PRACTICES
PURPOSE
The goal of the Employee Health and Safety Code ofManagement Practices is to protect and promote the health and safety of people working at or visiting member company work sites.
To achieve this goal, the Code provides Management Practices designed to continuously improve work site health and safety. These practicesprovide a multidisciplinarymeans to identify and assess hazards, prevent unsafe acts and conditions, maintain and improve employee health, and foster communication on health and safety issues.
Implementation of the Employee Health and Safety Code, together with other Codes ofManagement Practices, can enable member companies to operate in a manner that further protects and promotes the health and safety of employees, contractors, and the public, and protects the environment.
RELA TIONSHIP TO GUIDING PRINCIPLES
Implementation of the Code helps achieve several of the Responsible Care* Guiding Principles:
I To recognize and respond to community concerns about chemicals and our operations.
I To make health, safety, and environmental considerations a priority in our planning for all existing and new products and processes.
I To operate our plants and facilities in a manner that protects the environment and the health and safety of our employees and the public.
I To extend knowledge by conducting or supporting research on the health, safety, and environmental effects of our products, processes, and waste materials.
DSU IX) 8 063
R. Page 11 of 98
WATER_PCB-SD0000021771
MANA CEMENT PRA CTJCES
Each member company shall have an ongoing occupational health and safety program that includes:
Program Management
1. Commitment by all levels ofmanagement to protecting and promoting the health and safety of people working at or visiting member company work sites through published policies; accountability for implementation; and provision of sufficient resources, including qualified health and safety personnel
2. Opportunities for employees to participate in developing, implementing, and reviewing health and safety programs.
3. Provisions, including selection criteria, to confirm that on-site contractors' programs are consistent with applicable Management Practices ofthis Code.
4. Written, up-to-date health and safety programs and procedures appropriate to the facility.
5. Means to verify that health and safety programs and procedures are effective and that actual practices are consistent with these programs and procedures.
6. Systems for maintaining records and analyzing data to evaluate health and safety perfor mance, determine trends, and identify areas for improvement
Identification and Evaluation
7. Methods to identify and evaluate potential health and safety hazards in planned or existing facilities, ineluding facilities to be modified.
8. Exposure assessments and safety analyses to evaluate health and safety hazards to employ ees from processes; equipment; potentially hazardous chemical, physical, or biological agents; or other work site conditions.
9. Health assessments to determine employee medical fitness for specific job tasks.
10. Employee occupational medical surveillance programs tailored to work site hazards.
Prevention and Control
11. Mechanisms for reviewing the design and modification offacilities andjob tasks, taking into account the foDowing hierarchy of controls: inherent safe design, material substitution, engineering controls, administrative controls, and personal protective equipment.
12. Systems to verify that health and safety equipment is properly selected, maintained, and used.
R. Page 78 of 98
05m 108064
WATER_PCB-SD0000021772
13. Preventive maintenance and housekeeping programs to maintain the safety of facilities, tools, and equipment.
14. Timely investigation of work site illnesses, injuries, and accidents; corrective actions to prevent recurrence; and evaluation of the effectiveness of corrective actions taken.
15. Security procedures end systems to control entry and exit of personnel and materials at the work site and restricted areas.
16. Provisions for emergency medical assistance for people at work sites.
Communications and Training 17. Communication ofhealth and safety information that is relevant to specificjob tasks and the work site.
18. Health and safety training programs, including documentation of these programs, and methods to evaluate the effectiveness of both training and communications activities.
INDUSTRY TREND DA TA To identify industry trends, eaeh company shall report to CMA, or its designated agent, occupational injuries and illnesses, as specified in CMA's Occupational Injury and Illness Reporting Program.
RELATIONSHIP TO OTHER CODES OF MANAGEMENT PRACTICES This Code complements, and should be implemented in conjunction with, current and future Codes of ManagementPractices, especially those elements ofthe CAER Code involving emergency response, the Process Safety Code involvingtrainingofemployees in theirjob functions, and the Product Stewardship Code involvinghealth, safety, and environmental information, and employee education and product use feedback.
MEMBER SELF-EVALUATION
Each member company shall report annually to CMA, or it* designated agent, the implementation category attained for each Management Practice in this Code. The reports should be submitted on the member self-evaluation form provided.
RESOURCE GUIDE
A separate resource guide is available to assist member companies in implementing the Code.
Th Responsible Care* Employes Health 4 Safety Code of Management Practices era* approved by CMA * Board of Director* on January 14.1092
DSW 108065 R. Page 79 of 98
WATER_PCB-SD0000021773
R. Pge 80 of 98
OSW 108066 .
WATER PCB-SD0000021774
Responsible Care: A Public Commitment
EMPLOYEE HEALTH AND SAFETY CODE OF MANAGEMENT PRACTICES
MEMBER SELF-EVALUATION FORM
Member Company Name;
Responsible Care* Coordinator Name: Address:.
Telephone: I____ 1
Number of facilities subject to the Employee Health and Safety Code:.
DSW 108067
R. Page 8) of 98
WATER_PCB-SD0000021775
R. Page 82 of 98
DSW 1<>8060 WATER PCB-SD0000021776
EMPLOYEE HEALTH AND SAFETY CODE
MEMBER SELF-EVALUATION FORM
Instructions for the Company Responsible Care* Coordinator 1. This form is to be submitted annually to CMA by each member company.
2. Indicate on page 1 the number ofyour member company's facilities that are subject to the Code. Each company must report the implementation stage for all facilities subject to the Employee Health and Safety Code on this form.
3. For each Management Practice en the following pages, indicate the number offacilities that have attained each implementation category. Each facility should appear in only one implementation category per ManagementPractice. Identify the currentimplementation category for each ofyour facilities at the time you complete the form.
4. For the Industry Trend Data, reportthe previous calendaryear's cumulative occupational injuries and illnesses. Occupational injuries and illnesses should be reported on a company wide basis as specified by CMA's Occupational Injury and Illness Reporting (OUR) Program.
5. Only subject facilities owned or operated as of the reporting date should be included. 6. The implementation categories are:
Category NA -- No action. If mo action taken because ike Management Practice is mot appli cable, please explain in apace marked Vonuewls."
Category EV - Evaluating existing companypractices againet the Management Practice. Category DP - Developing plan to implement Management Practice. Category lA - Implementing action plan. Category PP - Management Practice in place. Category El - Peaseeming Management Practice implementation.
SW 108069
R. Page 83 of 98
WATER_PCB-SD0000021777
Pape 84 of 98
DSW 108070
WATER PCB-SD0000021778
EMPLOYEE HEALTH AND SAFETY ,,____________C_ ODE OF MANAGEMENT PRACTICE,,S Sy>4f%
NA !V W IA PP HI 1. Commitment by all levels of management to protecting and
promoting the health and safety of people working at or visiting membercompany sites, through; published policies;accountably ity for implementation; and provision of sufficient resources, including qualified health and safety personnel Comment* an Catesrorv NA:
2. Opportunities for employees to participate in developing, imple menting, and reviewing health and safety programs. Comments on Category NA_*
3. Provisions, including selection criteria, to confirm that on-site contractors' programs are consistent with applicable Manage ment Practices ofthis Code. Comments on Cateeorv NA:
4. Written, up-to-date health and safety programs and procedures appropriate to the facility.
Comment! on Category NA
Cipfy NA
Cawpfy tv
Cawpt) DP
Cm>(7 IA Cat#ff7 PP
CtapT W
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OSH 1X380 7.1 R. Pape 85 of 98
WATER_PCB-SD0000021779
Management Practice*
Categories
NA EV DP IA PP ri
5. Means to verify that health and safety programs and procedures are effective and that actual practices are consistent with these programs and procedures.
Comments on Category NA-
. Systems for maintainingrecordsandanalyzingdatatoevaluate health and safety performance, determine trends, and identify areas for improvement.
Comments on Category NA-
7. Methods to identify and evaluate potential health and safety hazards in planned or existing facilities, including facilities to be modified.
Comments on Category NA-
6. Exposure assessments and safety analyses to evaluate health and safety hazards to employees from processes; equipment; poten tially hazardous chemical, physical, or biologies] agents; or other work site conditions.
Comments on Category NA
9. Health assessments to determine employee medical fitness for specific job tasks.
Comments on Category NA
Cjwpry NA Ctupty EV Catrfry Of C*up>y IA
r>wpt} fr
c-f-viu
R. Pape 86 of 98
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Ds*
fUla.
108072
WATER_PCB-SD0000021780
Management Practice*
Categories
NA EV DF IA PP HI
10. Employee occupational medical surveillance programs tailored to work site hazards.
Comments on Category NA:
1L Mechanisms for reviewing the design and modification offacili ties andjob tasks, taking into account the followinghierarchy of controls: inherent safe design, material substitution, engineer* ing controls, administrative controls, and personal protective equipment.
Comments on Category NA:
12. Systems to verify that health and safety equipment is properly selected, maintained, and used.
Comments on Category NA:
13. Preventive maintenance and housekeeping programs to main* tain the safety offacilities, tools, and equipment.
Comments on Category NA.-
14. Timely investigation of work site illnesses, injuries, and inci dents; corrective actions to prevent recurrence; and evaluation of the effectiveness of corrective actions taken.
Comments on Category NA:
na
EV C<upn DP
Cm>(7 LA Cip>> PP
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N Mte, IfMaalMBLnhMwIk)
Pw<n It --ppph--Sh. ylw wyUI*
Smhutlac bMlaff Mpq ywali tplai eMmplhirtn.
DmlapOif piaa m lapirat Maupanl Pimm.
iBybamtat meetmm ylu ,
taalai
CSW 108073
WATER PCB-SD0000021781
Management Practices
Categories
NA ev DP IA M *1
15. Security procedures and systems to control entry and exit of personnel and materials at the work site and restricted areas.
Comments on Category NA:
16. Provisions for emergency medical assistance for people at work
sites.
.
Comments on Category NA:
17. Communication ofheahh and safety information thatis relevant to specific job tasks and the work aite. Comments on Category NA:
18. Health and safety training programs, including documentation of these programs, and methods to evaluate the effectiveness of both training and communications activities. Comments on Category NA:
INDUSTRY TREND DATA
Occupational Injuries and lllnessesforthe previous calendaryearwere reported as specified
in CMA's Occupational Injury and Illness Reporting Program.
Yes____
No____
"
If no. please explain:
_______
CcMfvry NA CsMfvfy EV fmpr) DP
ftmm u fnf7 rr
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Page 88 of 98
Mltn IfwHlw UfaaW--SihibiH
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it frtcUn togfai
li ini;;llrili jlmi OSH 1080 7**
WATER PCB-SD0000021782
QUESTIONS AND ANSWERS
EMPLOYEE HEALTH AND SAFETY CODE OF MANAGEMENT PRACTICES
Throughoutits development, theEmployee Health and Safety tfchbj Code wii reviewed regularly by CMA'i Health and Safety Committee, Engineering and Operation* Committee, and Responsible Care*CoordinatingGroup. An earlydraftoftbeEHS Codewasreviewedbymember companies through written comments and an open meeting, and member companies conducted a second review ofthe draft EHS Code with their employees. In addition, the draft EHS Code was reviewed periodically by the Responsible Care* Public Advisory Panel
During these reviews, the foDowing questions were frequently asked about the EHS Code of Management Practices:
1. Does the EHS Code oover all aspects of an employee's health and safety?
Answer. The EHS Code is restricted to those aspects ofan employee's health and safety that are affected by his orher employmentin the chemical industry. The EHS Code addresses occupational health and safety and does not address employee wellness or eff-the-job safety.
2. Does the EHS Code include visitors and all contractor operations?
Answer. The EHS Code covers all visitors and contractor employees who enter a member company's work site. Visitors should be protected from hazards they may encounter while on the work site. All contractors should have health and safety programs for their employees that are appropriate forthe hazards encountered in their contractedjob tasks and that are consistent with applicable management practices of die EHS Code. Contract manufacturers, or tollers, are addressed in the Produet Stewardship Code.
3. Does the EHS Code require employee participation at work sites at which employees are represented by a union?
Answer. The objective of the EHS Code is to encourage member companies to fully involve employees in safety and health activities. However, at facilities at which employees are represented by a union, negotiations concerning such employee participation may be required. In the contract negotiation process, member companies should make a good-faith effort to address opportunities for employee participation.
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4. What is CMA's Occupational Injury and Ulnesa Reporting (OUR) Program?
Answer-. CMA's OIER Program serves as a basis for swarding the annual Lammot Du Pont Safety Awards recognizing sustained achievement by CMA member companies in reducing workplace injury and illness rates. Each participating company submits its injury and illness data, as reported on the OSHAForm 200, based on guidelines issued by the U.S. Bureau ofLabor Statistics
(BLS).
I
5. Are contractor employees included in the OUR Program?
Answer-. At this time, contractor employees are not included in the CMA OIIR Program, unless
the company directly supervises their day-to-day activities. Current BLS guidelines require
reporting of occupational injuries and illnesses by individual employers based on Standard
Industrial Classification (SIC) codes. Both CMA and OSHA are considering revisions to the
reporting guidelines that would consolidate the reportingofoccupational injuries and illnesses for
a single work site, without regard to the SIC code of the employer.
.
6. Does the EES Code address substance abuse in the workplace as part of assessing medical fitness for specific job tasks?
Answer. Substance abuse is addressed by the Process Safety Code in Management Practice 21: `Programs designed to assure that employees in safety-critical jobs are fit for duty and are not compromised by external influences, ineluding alcohol and drug abuse."
7. Does the EHS Code require job tasks to be evaluated for physical requirements?
Answer-. Job tasks should be evaluated to determine the specific physical abilities associated with a task. An employee's abilities should be evaluated using medical criteria before being assigned to a job task with specific physical requirements. For example, employees should be medically evaluated to determine their ability to wear a respirator before being assigned to job tasks requiring the use of a respirator.
8. Does the EHS Code require member companies to provide
medical examina
tions to all employees as part of an occupational medical surveillance program?
Answer. No. Occupational medical surveiUanee programs should provide appropriate, targeted medical assessments to those employees exposed to specific hazards. For example, regular spirometry examinations to assess lung function should be offered to employees exposed to an agent known to affect lung function.
9. Does the EHS Code require member companies to assess the effect of exposures to chronic hazards on the health of employees?
Answer. As s part of maintaining records and analyzing data for trends, member companies should assess the long-term health experience of their employees in relationship to exposures to chronic hazards. Chronic hazards include, for example, long-term exposures to carcinogens.
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OSH 1080.76
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MIE PRODUCT STEWARDSHIP CODE
Product Stewardship Booklet for the Code of Management Practices
The code's management practices are grouped into three categories, described as
follows:
Management Leadership and Commitment contains Management Practices 1-3. These practices serve to give direction, provide resources, set priorities, and establish responsibilities within your company that provide an appropriate atmosphere and founda tion for successfully implementing product stewardship.
Information and Characterization includes Management Practices 4 and 5. These address the need to continually increase the body of knowledge surrounding chemical products in order to improve hazard identification and risk characterization at every stage
in a product's fife.
As the cornerstone of product stewardship. Management Practices 6-12 are categorized as Risk Management practices, which work together to manage risks at every stage of a product's fife. Some of these management practices are the most chalenging in the Code because they extend the risk management process beyond traditional boundaries to consider risks beyond the point of sale.
Management practices in the first two categories provide the foundation tor conducting the risk management practices in the third category. The ability to implement each management practice, therefore, relies upon the successful implementation of previous practices, with the successful development and implementation of product stewardship progressing from a planning and resource allocation to an information collection phase, and finally to action-oriented, risk management activities.
Purpose and Scope
The purpose of the Product Stewardship Code of Management Practices is to make health, safety and environmental protection an integral pan of designing, manufacturing, marketing, distrfoufing, using, recycling and disposing of our products. The code pro vides guidance as wed as a means to measure continuous improvement in the practice of product stewardship.
The scope of the code covers all stages of a product's fife. Successful implementation is a shared responsibility. Everyone involved with the product has responsibilities to address society's interest in a healthy environment and in products that can be used safely. All employers are responsible for providing a safe workplace, and all who use and handle products must follow safe and environmentally sound practices.
The code recognizes that each company must exercise independent judgment and discretion to successfully apply the code to its products, customers and business.
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Relationship to Responsible Care and Guiding Principles
Implementation of the code promotes the achievement of several of the Responsible Care* Guiding Principles:
to make health, safety and environmental considerations a priority in our planning for all existing and new products and processes:
. to develop and produce chemicals that can be manufactured, transported, used and disposed of safely;
, to extend knowledge by conducting or supporting research on the health, safety and environmental effects of our products, processes and waste materials:
to counsel customers on the safe use, transportation and disposal of chemical products;
to report promptly to officials, employees, customers and the pubGc, information on chemical-related health or environmental hazards and to recommend protec tive measures;
to promote the principles and practices of Responsible Care* by sharing experi ences and offering assistance to others who produce, handle, use, transport or dispose of chemicals.
This code complements, and should be implemented in conjunction with, current and future Codes of Management Practices. Chapter 3 discusses the Product Stewardship Code's relationship to the other existing codes.
Management Prictices
Management Practice 1
LEADERSHIP: Demonstrates senior management leadership through written policy, active participation and communication.
The objective of this management practice is to set the driving force for the Product Stewardship Code. To this end, senior management must first adopt a policy that reflects the company's vision of product stewardship. This.policy should state dearly how senior management expects product stewardship to be managed within the com pany.
To be effective, the policy should emphasize that product stewardship, like quality and safety, must be woven into the company's culture, h also should be dear that the commitment is an ongoing, long-term part of the company's operations and business.
Finally, if the new policy represents a change in the way of doing business. It should be dear that a change in behavior is expected. In some companies, a separate written product stewardship policy may be effective. In others, a broader health, safety and environmental (H.S&E) policy that incorporates the prindples of product stewardship may be more appropriate.
However, a policy alone is not enough. The words of a policy must be reinforced by actions and behaviors that continuously reaffirm the goals senior management has set Senior management is responsible for conveying throughout the organization its involve ment with, and support of. product stewardship--especially to the next level of manage-
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Tl IE PRODUCT STEWARDSHIP CODE
merit and encouraging it to do the same. (Management Practices 2 and 3 locus on some of the visible signals - tor example, goals, performance measurement and resource
allocation).
Management Practice 2
.
ACCOUNTABiLTTY and PERFORMANCE MEASUREMENT: Establishes goals and responsibilities tor Implementing product stewardship throughout the organiza
tion. Measures performance against these goals.
One of the key ways senior management can convey the importance of product steward ship is by establishing it as a priority in business planning and individual performance planning. The objective is to develop a process that win result in continuous improve ment through goals that are welt-defined, achievable and measurable. Similarly, indi vidual responsibilities should be dear and consistent.
Management Practices
RESOURCES: Commits resources necessary to Implement and maintain product stewardship practices.
The commitment of resources, both human and financial, is a critical signal that manage ment can send to show its commitment to product stewardship practices and is a vital component for some implementation activities. Undoubtedly, resources will vary from company to company. However, in all cases, the commitment of resources should be consistent with product stewardship implementation plans and sufficient to support continuous improvement
Management Practlce4
HEALTH, SAFETY and ENVIRONMENTAL INFORMATION: Establishes and main tains Information on health, safety and environmental hazards and reasonably foreseeable exposures from new and existing products.
Just as Management Practice 1 is the driving force for the Product Stewardship Code. Management Practice 4 is the foundation. The objective of Management Practice 4 is to establish a knowledge base of human and environmental hazards and reasonably foreseeable exposures and, once established, to maintain it Under this practice, compa nies gather information to support the system that characterizes a product's risk (Man agement Practice 5) and. ultimately, the system that develops the methods to manage that risk (Management Practice 6).
Initially, some companies may establish their knowledge base by developing information; others may do so by collecting and compiling available information. However, all compa nies should have a process to continuously gather relevant product information and to review existing information to determine if it is accurate, cunent and complete.
Sources of information may indude published, unpublished and/or internally generated scientific reports on health, safety and environmental effects and exposures. Generally, the types of information could cover animal or human toxicity, ecotoxidty and chemical and physical properties that affect exposure or the environmental impact. In many cases, exposure information is not directly available but may be estimated with product use information.
Information on a product's handling, use and reasonably foreseeable exposures in research, development, manufacturing, transport, storage, packaging and disposal may
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be obtained by a number of means. These could include surveys of customers ano otneproduct receivers, technical reviews or visits to customers, and'or observations reponec by sales and marketing personnel.
Management Practice .5
PRODUCT RISK CHARACTERIZATION: Characterizes new and existing products with respect to their risk using Information about health, safety and environmental hazards and reasonably foreseeable exposures. Establishes a system that ini tiates re-evaluation.
This practice has two objectives. The first is to use the information gathered in Manage ment Practice 4 to develop a thorough understanding of the product's risk. This charac terization may be either quantitative or qualitative. The second objective is to establish a system that triggers re-evaluation, whether upon receipt of new information or upon periodic, scheduled review.
A product may be characterized as a single entity or it may be characterized in a group of products based on similar uses, compositions or physical properties. Product risks may vary with different uses or exposures.
The time frame for re-evaluation may vary from product to product. Triggers for such re evaluations might include significant new hazard or exposure data, significant new use or misuse information as it becomes known or a substantial increase in sales volume, suggesting new uses or markets.
Management Practice 6
RISK-MANAGEMENT SYSTEM: Establishes a system to Identify, document and Implement health, safety and environmental risk-management actions appropriate to the product risk.
The objective of Management Practice 6 is to establish a system for identifying and implementing risk-management actions. Risks involved in the production and use of chemicals can be managed and controlled if each company takes the basic information on a product's risk (Management Practice 4), characterizes it (Management Practice 5) and then implements a series of risk management actions (Management Practice 7 through 12). These risk management actions are a result of a conscious weighing of technical, ethical, societal and business issues surrounding a product Actions taken as a result can range from no action, to providing MSDSs and labels, to product reformula tion or repackaging, to removal of the product from a market.
The management practices that follow. Management Practices 7 through 12. are specific areas of company operations that warrant discussion and special emphasis.
Management Practice 7
PRODUCT and PROCESS DESIGN and IMPROVEMENT: Establishes and main tains a system that makes health, safety and environmental Impscts--including the use of energy and natural resources--key considerations In designing, developing and Improving products and processes.
Designing products and processes (or redesigning existing products and processes) with a system to identify health, safety and environmental impacts throughout the product lifecycle is one of the most effective ways of managing the product risks identified in Management Practice #5. One objective of this Practice is attainment of the preferred
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11IE PRODUCT STEWARDSHIP CODE
environmental hierarchy: source reduction: reuse: recycling: and disposal. Source reduction includes equipment or technology modifications, process or procedure changes, product reformulation or design, substitution of raw materials, and improvemerits in housekeeping, maintenance, training or inventory control.
This Practice also addresses the need for proper energy and natural resource utilizationimponant considerations for reducing potential adverse environmental impacts and achieving sustainable development.
The health, safety and environmental attributes of the product throughout its entire life cycle should be addressed at the beginning, during the concept and design (or redesign) phases. Re-evaluation should occur on a periodic basis or whenever changes to the
product or process are contemplated.
Insights and contributions from employees in all functional areas that may affect health,
safety and the environment should be incorporated into the review. These functional
areas include research and development, manufacturing, distribution, sales and market
ing and regulatory personnel.
'
Management Practice 8
EMPLOYEE EDUCATION and PRODUCT USE FEEDBACK: Educates and trains employees, based on }ob function, on the proper handling, recycling, use and disposal of products and known product uses. Implements a system that encour ages employees to feed back Information on new uses, Identified misuses or adverse effects for use In product risk characterization.
This practice has two parts. The first is to ensure that all employees who are involved with products have the training and education necessary to understand product (and packaging) hazards, proper use, handling, reuse, recycling and disposal procedures. The second is to help ensure that any new information that may alter the way risk is being managed is factored into the risk characterization process on a timely basis (Management Practice 5).
The training and education of employees should be tailored to specific job functions. For example, marketing and sales personnel are in a unique position to know how customers are using products and must be aware of product hazards, reasonably foreseeable exposures, appropriate uses and proper handling procedures. They should be able to identify product deviations and to recognize adverse health or environmental effects. These personnel should be alert to the customer's and the public's comments or percep tions.
It is essential that there be timely feedback of this safety, health or environmental infor mation or concerns into the risk characterization process (Management Practices 4 and 5). This feedback may change the risk management actions (Management Practice 6).
Management Practice 8
CONTRACT MANUFACTURERS: Selects contract manufacturers who employ appropriate practices tor health, safety and environmental protection tor the operations under contract, or works with contract manufacturers to help them implement such practices. Provides information and guidance appropriate to the product and process risk to foster proper handling, use, recycling and disposal. Periodically reviews performance of contract manufacturers.
The objective of this Management Practice is to encourage the use of contract manufac turers who have sound health, safety and environmental practices for the specific opera
tions under contract.
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The level of involvement will vary according to the product's risk. Actrvmes could inctuae reinforcement of previously provided health, safety and environmental information, additional training, etc. At a minimum, both parties should share any accumulated knowledge that would enhance health, safety and environmental protection.
The transmittal of appropriate information* acknowledges that while we want customers to pass along H.S&E information, product changes made by the customer may mean that the information originally supplied with the product no longer applies. In these cases, the customer needs to issue information that reflects the current H.S&E informa tion.
Along with Management Practices 9,10 and 11. this management practice constitutes an important outreach component of the Product Stewardship Code. The long-term result of implementing this practice. Eke the other outreach management practices, should result in improved health, safety and environmental performance - not just for CMA member companies but the entire chemical industry.
As with distributors and suppliers, reviews of customers will be commensurate with product risk. However. M Is appropriate to expect companies to extend the principles of product stewafdship beyond the CMA membership and Responsible Care*panners.
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MONSANTO PLEDGE GUIDELINE
#1
POLLUTION PREVENTION
The company will work toward the ultimate goal ofensuring zero effect attributable to waste in all media. It will research, design and operate its facilities to minimize the generation ofprocess and nonprocess waste and the potential effect ofchemical releases to the environment. For waste and releases that remain, the company will comply with regulations, while minimizing environmental threat and long-term liability.
KEY RESULTS
Reduce by 90 percent the company's 1987 level of worldwide air emissions of chemicals named by the United States Environmental Protection Agency (USEPA) tinder Title III of the Superfund Amendments and Reautborization Act (SARA Section 313) and chemicals of local concern outside the United States by the end of 1992.
Reduce by 70 percent the company's worldwide SARA Section 313, European Community Priority Pollutant List (EC 129) and carbon monoxide chemical releases to all media and off-site transfers by the end of 1995.
Discontinue the deep-well injection of Resource Conservation and Recovery Act (RCRA) hazardous waste streams and SARA Section 313 toxic chemicals by the end of 1999.
PROGRAM
1.1 Process Waste
The operating units will integrate into their release reduc tion plans the corporate goal of reducing all toxic and hazardous releases and emission to all media, working toward an ultimate goal of zero effect. For reducing releases from processes, the order of preference is source reduction, followed by reuse, recycling or co-product sale, and finally by incineration or other treatment to reduce the volume and/or toxicity of pollutant streams.
The development and use of technologies that improve
competitive positions will be emphasized.
'
The operating units will integrate into their releasereduction plans the following corporate goals:
Reduce by 90 percent the company's 1987 level of worldwide air emissions of SARA Section 313 chemicals and chemicals of local concern outside the United States by the end of 1992.
Reduce by 70 percent the company's worldwide SARA Section 313, EC 129 and carbon monoxide chemical releases to all media and off-site transfers by end of 1995. The January 1990 SARA 313 and EC 129 lists plus carbon monoxide apply through the end of the multimedia release reduction program.
An effect-based release reduction target will be establisbec every five years beginning in 1995, working toward an ultimate goal of zero effect By the end of 1993, a method and process for an effect-based reduction program for toxic chemicals will be developed.
1.2 Nonprocess Waste
Each facility will maintain an inventory of all nonprocess sources of waste generation, including power generation, office and maintenance operations, general warehouse trash, packaging/shipping materials and similar sources.
MONSANTO COMPANY
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1J Underground Well (Deep-well) Injection
The company will discontinue deep-well injection of RCRA hazardous waste streams by the end of 1999. It will also apply best feasible technology to virtually eliminate the deep-well injection of SARA 313 chemicals. The company's name will not appear on the list of companies making significant use of injection wells for disposal of SARA chemicals for the reporting year 2000 and beyond. The company will demonstrate progress by achieving in 1996 an 80 percent reduction of injected SARA chemicals against the 1990 base reporting year.
To be prepared for the possibility of mandatory regulations, the company intends to select by the end of 1995 optimal technical strategies for total withdrawal from deep wells. This preparation will include studygrade estimates to achieve non-brine, treated surface discharge. All operating units will continue where possible to challenge the technical impediments to total withdrawal from deep wells.
No new uses of deep wells for hazardous or toxic materials are permitted. A "new" use of deep wells is defined as injection of streams from new products or the addition of substances not previously injected at that site. New internal or external uses of deep wells for nonhazardous wastes and nontoxic chemicals will be considered by the Environmental Policy Committee (EPC) only on an exception basis and within the constraints of these guidelines. The economics of any project appropriation request for such use must be based on disposal technology other than the use of deep wells.
1.4 Polychlorinated Biphenyls -- "PCB-Free"
All company-owned sites (e.g., warehouses, plants, offices) located in the United States will minimize the potential for releases of polychlorinated biphenyls (PCB) by becoming "PCB-free" of Toxic Substances Control Act (TSCA)-contaminated articles by the end of 1994.
1.5 Land Disposal
Landfill of "acutely hazardous" wastes1 and "incinerables"2 will not be practiced. For hazardous wastes and wastes managed as hazardous, fixation of particularly mobile, persistent or bioaccumulative wastes will be accomplished whenever warranted and
feasible. In making the decision to manage wastes as hazardous, the company will take into account public expectations, emerging trends and worldwide company practice regarding the same or similar wastes.
Contractors hired for land disposal of process wastes will be subject to contracting and assessment requirements (see Pledge Guideline No. 7. Outside Processors). In the United States, the use of off-site hazardous waste landfills will be approved by the Environmental Policy Committee and will be limited in number.
Medical wastes generated at the company's locations will be incinerated prior to land disposal of residues. Assurance of incineration will be obtained via manifests or equivalent documents if manifests are not available.
The use of Monsanto facilities to commercially treat, store or dispose of non-Monsanto wastes is normally discouraged. Any such use or joint ventures (other than in site guest/host relationships) for waste management must be reviewed and approved by the Environmental Policy Committee.
Proposals for land application of process by-products
and residues, for beneficial use or disposal, should be
guided by the "Monsanto Guidance Document: Land
Application of Process By-Products and Residues." The
ESHA (formerly EC-201/202) discipline will be
followed for such proposals, including 5-year reviews.
New applications must be approved by the appropriate
Directors of Manufacturing and Environmental
operations; the Environmental Policy Committee must
approve if beneficial use is not included.
.
Each company location will maintain a record of both the on-site and the commercial waste treatment, storage and disposal sites it uses.
1.6 Air Emission and 'Water Release Assessments
The company will conduct and maintain an ongoing assessment of potential human health impacts for selected, routinely emitted air pollutants. It will develop appropriate control strategies to reduce identified, potentially unreasonable risk of harm to human health in surrounding communities. The list of air pollutants to be studied include: a) those listed under Section 112(b) of the U.S. Clean Air Act; b) those for which the
1 Aj lined in 40 CFR 261.33(e), plus any mixtures containing greater than 5 percent. 3 Hazardous wastes, or wastes managed as hazardous, with a heat of combustion greater than 6000 BTU/lb.
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USEPA has established cancer unit risk values: c) those contained on the International Agency for Research on Cancer (IARC) group 1 and 2A lists: d) other sitespecific pollutants identified by the plant that appear to warrant consideration (including those in significant quantities reportable via SARA Section 313). Plants outside the United States will use the above-given pollutant list plus any additional air pollutants on any local regulatory list that the plant manager deems important
Each plant will maintain a list of all such air pollutants, ranked by established and approved protocols. Depending upon the pollutant's relative ranking and if required by the protocols, the plant will use appropriate dispersion modeling techniques to determine potential maximum downwind concentrations for each such pollutant at specified receptors representative of the exposed population utilizing appropriate dispersion modeling techniques. Appropriate assessments of potential human health impacts at the community receptor points will then be analyzed according to protocols established by the company's Environmental, Safety and Health staff. Any potentially unreasonable risk to human health that is identified will be expeditiously reduced to acceptable levels through appropriate actions.
The company will conduct aquatic safety assessments to determine the measurable impacts, if any, of its effluents on receptor water quality. The assessments should include both direct and indirect discharges (if applicable) with the mitigating impacts of the publicly owned treatment works (POTW) taken into account for the indirect discharge assessments. Any potentially unacceptable impacts to the aquatic environment identified will be mitigated in a timely maimer. A reconfirming assessment will be conducted to verify that the impacts have been reduced to acceptable levels.
All initial air emission and surface water release assessments required should be conducted for each of the company's worldwide manufacturing sites within two years of the EPC's approval of this guideline. Operating units will review the status of the assessments annually, and if any significant changes have occurred at a plant site, determine whether the assessment should be repeated. Any such reassessments will be completed within 12 months.
1.7 Measurement The following indicators will be used to measure progress against this guideline:
1.7.1 Annual progress toward achievement of 90 percent SARA Section 313 air emissions reduction goal.
1.7.2 Annual progress toward achievement of 70 percent worldwide SARA Section 313 chemical releases and off-site transfer reduction goal.
1.7.3 Achievement of contingency planning for reduction of use of deep-well injection.
1.7.4 Annual progress toward goals involving discontinued deep-well injection of RCRA hazardous waste streams and toxic SARA Section 313 chemicals.
1.7.5 Air Emissions and Water Release Assessments
The company's air and water steering committees will be responsible for tracking the air emission and water release environmental assessments conducted at each site and maintaining an ongoing list of the assessments' current status. In addition, Li'' plant's environmental compliance audit will check the current status of these assessments and report on progress as part of the audit's findings.
1.8 Coordinators
Where clarification is required, the following coordinators should be contacted:
WASTE MANAGEMENT D. B, Redington, ESH, Corporate, A3NA (314) 694-6503.
ASSESSMENT C. D. Malloch, ESH, Corporate, A3NA (314) 694-8889.
(Revised and approved by the Environmental Policy Committee, February 18,1994.)
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