Document YjQgNZ27xNY65rKBDRZpBey78
MINUTES OF MEETING CMA EXECUTIVE COMMITTEE Innisbrook Hotel, Tarpon Springs, Florida
January 7, 1980
1. The meeting was called to order at 1:00 p, m. by the chairman. There were present:
H. Barclay Morley, Chairman J. Earl Burrell Louis Fernandez John M. Henske Richard J. Hughes William C. Krumrei
Duncan J. MacLennan L. John Polite, Jr. Robert A. Roland William G. Simeral Raymond C. Tower
Bruce M. Barackman, Secretary Gary C- Herrman, Treasurer Edmund B. Frost, General Counsel
By Invitation; Timothy F. Burns, CMA Geraldine V. Cox, CMA H. A. Ericson, Monsanto Company John T. Estes, Allied Chemical Corporation Richard F. Gold, Stauffer Chemical Company Stephen L. Goldstein, Olin Corporation Keith R. McKennon, The Dow Chemical Company K. James O'Connor, Jr. , CMA Victor H. Peterson, CMA Edward B. Poliak (SOCMA), Olin Corporation James N. Sites, CMA William M. Stover, CMA David F. ZoU, CMA
**## ## *
After excusing invitees and staff, except for Messrs, Barackman and Frost, the committee convened in executive session during which the apparent difficulties resulting within CSMA because of the CMA name change were discussed. Following this, the committee then proceeded with the agenda items in regular session.
#*#
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2. Minutes of the Last Meeting The minutes of the November 19, 1979, meeting of the Executive Committee, as distributed, were approved.
3.
Treasurer's Report
Mr. Herrman's report is attached as
Exhibit A. He announced that the request for 1979 chemical sales data,
upon which fiscal 1980-81 dues will be based, is in the mail. The budget
process is under way. It is planned to mail a preliminary budget on
February 25 for consideration at the March meeting.
4. Review of Committee Reports to the Board noted that;
Mr. Morley
The Energy Conservation Committee recommended that its name be changed to Energy Affairs Committee which more accurately reflects the current broadened scope of activities.
Following discussion, a change of name to Energy Affairs Committee or simply Energy Committee, as preferred by the committee, was approved.
The Patents and Information Retrieval Committee recommended it be restructured to eliminate information retrieval activities.
During discussion, matters involving other committees were included as well. The importance of evolving a priority system to discreetly pick those issues about which CMA should be most concerned and which would merit policy discussion at the Board level was recognized. It was decided to take no further action until the Audit Committee reports had been received. Meanwhile, staff was requested to come back to the Executive Committee with recommendations regarding committee structures and the mechan ics to provide an overview of emerging issues in areas where there are no committees.
5.
Super fund
Mr. Stover reviewed briefly developments in the
Congress, noting that little had changed since his last report. During his
report, attached as Exhibit B, he invited attention particularly to the re
lease into the environment concept as it relates to the funding issue, pages
8 and 9. Mr. O'Connor proceeded to make an economic analysis of various
bills pending.
Following discussion the Executive Committee:
Endorsed Superfund analysis in Exhibit B.
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Reaffirmed CMA position on Superfund and reemphasized the importance of maintaining a unified posture on that position, namely: The Association opposes the imposition of fees of any kind on industry; the problem of orphan disposal sites should be addressed through a fund financed by Federal and state money; and state tort law is adequate to address the personal injury problem. The priorities should be scope, liability, and funding in that order.
Directed Superfund Steering Committee to develop alternatives for Executive Committee consideration for use in the event that our present position should require modification.
Designated Mr. Fernandez of Monsanto as Executive Committee liaison to Superfund Steering Task Group,
6. Chemical Industry Communications/Public Support Program Mr. Roland introduced the subject by reading excerpts of letters from several companies predominantly in support of the program while noting some concern had been expressed about advertising.
Mr. Sites, during his report attached as Exhibit C, emphasized that the ad part of the program is essential to its effectiveness. He dis cussed the importance of member company involvement to a successful program. To aid such participation he announced that a Speakers Manual will be available soon and a special workshop will be held in Washington, D. C., Wednesday, February 13, for industry communication's personnel. Distributed to those present was a printed copy of "Transporting Chemicals Safely: What We're Doing About It" and a photo copy of a similar booklet being printed on the subject of "Protecting the Environment. " These are the first two in a series of four booklets being prepared for mailing to Executive Contacts, The others will concern worker safety and product safety.
Mr. Sites then discussed the need for additional structuring within CMA:
(a) To assure the Board/Executive Committee and member company executives of top-level policy and budget review and guidance, and
(b) To provide the maximum involvement in implementing this nationwide program by top member company communications professionals.
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Mr. Herman presented various alternatives for billing member companies in support of the program.
Following discussion, the Executive Committee;
Endorsed the communications program summarized in Exhibit C.
Approved establishment of a Communications Committee of 15 members to take the place of the present task group and oversee the communication's program and related association public re lations activities.
Recommended Board approval for the establishment of a group of 7 members to be called the Communications Policy Review Group to assure top-level budget and policy guidance for the program and suggested the following Board members as members;
J. Earl Burrell, President, PPG Industries, Inc. , and Chairman, CMA Finance Committee
Vincent L. Gregory, Jr., Chairman of the Board and Chief Executive Officer, Rohm and Haas Company
James B. Henderson, President and Chief Executive Officer, Shell Chemical Company
William C. Krumrei, Senior Director, Research and Development, The Procter & Gamble Company
L. John Polite, Jr,, Chairman of the Board and Chief Executive Officer, Essex Chemical Corporation
William G. Simeral, Senior Vice President, E. I. du Pont, de Nemours & Company
The group will also include Dr. Etcyl Blair, Vice President, Health and Environmental Sciences, The Dow Chemical Company, and Chairman of the Communications Program's Science Advisory Group.
7.
Recommended for Board approval that the funds for the program be raised by special assessments to be made in January 1980 of $2. 555 million and January 1981 of $3. 6 million, based on calen dar year 1978 and 1979 sales, respectively.
Association Activities
(a) CMA Meeting Sites
Various Semiannual meeting sites
for 1980-84, with dates prior to Thanksgiving week, were presented by
staff and discussed. Locations for the regional Board meetings in Septem
ber and January were also considered. The September 1980 meeting at
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Pebble Beach, California, September 8-9, having previously been con firmed, it was agreed that the January 1981 meeting would be at the Ocean Reef Club, Key Largo, Florida, January 5-6. With the benefit of views expressed during discussion, staff will proceed to obtain suitable accom modations through 1984 from among those available.
(b) Clean Air Act Revision - Retention of Consultants this item was deferred for Board consideration.
Action on
(c) Labeling
Mr. Zoll's report is attached as Exhibit D- He
emphasized that labeling will be among the most important issues facing
the chemical industry in 1980.
(d) Resignation of Mr. A. B. Trowbridge
On the occasion of Mr.
Trowbridge's resignation as Chairman of the Executive Committee and as
a member of the Board of CMA effective January 1, 1980, the Executive
Committee requested Mr. Roland to arrange for the presentation of a
suitable commemorative which would convey the Association's appreciation
for his valuable contributions to its activities.
8. New Business
(a) Name Liaison to the Office of Chemical Industry Trade Advisor This item was tabled.
(b) Committee Apointment
The appointment of Mr. Thomas F.
Evans, Monsanto Company, to replace Dr. W. J. McCarville on the
Occupational Safety and Health Committee for the term ending May 31,
1982, was approved.
C"
H. Barclay'Morley, Chairman CMA Executive Committee
Bruce M. Barackman Secretary
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TREASURER'S REPORT
Exhibit A
Seven Months Ending December 31, 1979
This report will be prepared and distributed following the end of the month.
For your reference, the following is provided:
The approved 1979-80 budget.
Year-to-date budget amendments in Special Projects, the Hazardous Waste Technical Center and the Environmental Management Committee's Air Program.
The revised total Budget for fiscal 1979-80 after amendments.
CMA EC-1/7/80 BD-1/8/80
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CHEMICAL MANUFACTURERS ASSOCIATION Budget For Fiscal Year 1979-1980
(As amended through December 31, 1979)
REVENUES:
Membership Dues & Entrance Fees
Investment Income General Meeting Income Publication Sales Overhead Reimbursement-
Subscribed Projects
TOTAL REVENUE
Original 1979-80 Budget
$ 7,298,800 555,500 129,000 153,700
250,000 $ 8,387,000
GENERAL OPERATING EXPENSES:
Salaries Employee Benefits Travel & Entertainment Printing & Reproduction Public Relations Furniture & Equipment Telephone & Telegraph Postage Taxes & Insurance Rent & Premises All Other
TOTAL
$ 2,696,700 523,200 160,900 377,400 96,500 185,700 128,000 149,300 373,900 218,000 131,600
$ 5,041,200
LEGAL & RESEARCH:
Legal Fees & Expenses Research & Consulting
TOTAL
$ 1,368,000 1,102,000
$ 2,470,000
TOTAL OPERATING EXPENSES $ 7,511,200
Approved Amendments
$-
-
104,800 $ 104,800
$ 186,500 34,000 53,100 15,500
-
27,200 5,300 2,800
27,100 13,200 13,600 $ 378,300
$_ -
$-
$ 378,300
Budget as
Amended
$ 7,298,800 555,500 129,000 153,700
354.800 $ 8,491,800
$ 2,883,200 557,200 214,000 392,900 96,500 212,900 133,300 152,100 401,000 231,200 145,200
$ 5,419,500
$ 1,368,000 1,102,000
$ 2,470,000
$ 7,889,500
EXCESS OF REVENUE OVER EXPENSES BEFORE COM MUNICATIONS PROGRAM
COMMUNICATIONS PROGRAM EXPENSES
CHANGE IN ASSOCIATION RESERVES
Projected Year-end Reserves Projected Reserves as a Percentage
of General Operations
$ 875,800
$ (273,500)
(250,000)
$ 625,800 $ 2,202,500
43.77,
$ (273,500) $ (273,500)
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$ 602,300
(250,000)
$352,300 $ 1,929,000
35.57,
Exhibit B
SUPERFUND: LEGISLATIVE STATUS UPDATE
Congressional hearings on Superfund and related bills are largely behind us and the next step in the legislative process is subcommittee markup.
In the House, the first formal markup began in Representative James Florio1 s (D-NJ) Subconmittee on Transportation and Conmerce on Decenber 13, 1979. Tfti session produced a flurry of activity and maneuvering, but no major decisions were reached. Hie vehicle for markup was Mr. Florio's H.R. 5790 which provides for emergency response to abandoned and inactive waste disposal sites, zero releases of hazardous wastes and substances into the environment, creates a fund financed primarily from taxes against the chemical and oil industries with contributions from Federal and state general revenues, defines a new scheme for RCRA interim permitted sites that become inactive, and establishes joint,several and strict liability to enable persons and governmental agencies to recover from responsible parties.
The Subcommittee staff developed technical changes to the original proposal which were offered as a substitute, and Representative Barbara Mikulski (D-MD) pro posed two amendments which were adopted.
Representative Robert Madigan (R-IL) failed in an effort to substitute a much more limited bill for the Florio bill. The Madigan substitute would have applied only to abandoned and inactive disposal sites, provided full funding from tax dollars earmarked from the tax royalties of the Outer Continental Shelf Act, established an emergency response and containment mechanism, ordered a state-by-state inventory of all sites be conducted and established strict lia bility for clean-up and containment. The Madigan substitute was defeated on a party line vote of 3 to 5.
The House Public Works and Transportation Subconmittee on Water Resources has taken no further action to date on H.R. 85, the oil spill Superfund Bill. Key questions before that subconmittee will be the creation of a Superfund for hazardous substances spills, and whether or not to meld such a fund with the ocean oil spills bill.
The Merchant Marine and Fisheries Conmittee, which originated H.R. 85, is thought to prefer enactment of a separate bil spill Superfund.
The Senate Ehvironment and Public Works' Subconmi ttees on Environmental Pollution and Resource Protection have not proceeded with formal markup of~ S. 1480 (Culver/Muskie). The Conmittee staff continues to hold in-depth dis cussions with various groups, including CMA, on the Superfund issues. CMA has thus far participated in six discussion sessions, bringing in technical, legal and legislative specialists to take part. These sessions will continue into January.
It is possible that when the Subcommittees begin markup early in 1930, a new staff re-drafted version of S. 1480 could be presented.
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2- The Affa-inistration and the Environmental Protection Agency (EPA) continue to pursue a Superfund that would include coverage of oil spills, hazardous sub stances spills and abandoned and inactive waste disposal sites. EPA continues to come under attack for its failure to provide concrete figures to justify its complex and massive approach. EPA still views Superfund as a top priority issue QA bag recently entered into discussions with merrbers of the Sierra Club, the Environmental Defense Fund, Congress Watch, and Environmental Action. These talks are aimed at exploring areas of Superfund where cannon ground mig^it be found.
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SUPERFUND: ECONOMIC ANALYSIS
Thursday, December 6, 1979, Mr. Roland wired members of the CMA Executive Committee requesting they designate a qualified representative to participate in an ad hoc working group to further explore the economic implications of Superfund legislation. The group was asked to focus on the degree to which common methodologies, conclusions or alternatives could be developed in measuring the possible impact of Superfund concepts.
In a December 13 meeting the group reached several broad conclusions and agreed on the outline of a report to be presented at the January 6, 1980 meeting of the CMA Executive Committee.
Outline of the report follows:
I. A comparison of the fees likely to be required under:
A. The Administration Bill (S. 1341)
B. The Florio Bill (H.R. 5790)
C. Two hypothetical waste disposal fee mechanisms:
(1) Disposal fee charged against hazardous wastes identified under RCRA;
(2) Disposal fee charged against hazardous wastes and special wastes identified under RCRA.
II. A comparison of the economic burden imposed on ten CMA member companies for each of the four scenarios listed above. Data are indexed against the cost of S. 1341 to protect individual company confidentiality. Agreement was reached on several common assumptions to be used in calculating the data.
III. Advantages and disadvantages of various fee/funding concepts: attention will be devoted to the feedstock fee approach, the waste disposal fee approach, and other possible fee mechanisms, such as chemical sales tax, transportation tax, etc.
Action Required:
Information only.
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SUPERFUIffi: ISSUES AND POLICY CONSIDERATIONS
Althauf^i many important questions have been raised during the course of the superfund debate, nearly all can be encompassed within three general issue areas: the scope of coverage, the standards of liability and the method of funding.
The scope issue involves two major considerations. First is subject matter coverage of the superfund program. Should it address only old dunpsite problems or should it also include future dunpsite problems, spills of hazardous substances of oil spills? Second is scope of relief. Should the program be limited to emer gency assistance and cleanup or should it go on to cover third party damages and a host of other items?
The standards of liability issue area raises several vital questions. Should there be joint and several liability or should there be a system with apportioned liability? Should there be strict liability with few defenses being allowed or should more defenses be provided? What standards of causation will be used, to determine whether a party is liable?
The third issue area is funding. Should the fund be financed out of Federal dollars? Should industry be required to foot the bill? Or should there be some combination of Federal and industry money? If there is an industry fee, hew should it be structured and imposed?
Following is a review of the key questions in each of these major issue areas.
I. SCOPE ISSUES
A. "Ultrafund"
Some Superfund bills adopt an extremely broad approach -- what has been referred to as "ultrafund" approach. They would combine oil spills, hazardous substance spills and hazardous waste disposal site problems into a single com pensation and liability fund. The usual justification is that administrative efficiency and public health would be enhanced by one conprehensive system; one program answers the need for immediate notification and response, emergency response actions; engineering techniques required for containment and remedy are substantially similar for spills of hazardous substances and oil; there are also substantial similarities between problems caused by hazardous wastes and waste oils at disposal sites.
B. The CMA Approach
CMA, on the other hand, has argued for separation of "ultrafund" into its constituent parts.
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- oil spills should be handled separately from chemical spills;
- chemical spills should be separated from waste disposal incidents;
- in addressing hazardous waste disposal sites, pre-RCKA problems should be separated from post-RCRA problems.
The rationale is that these subjects are each different in nature, and are addressed in differing degrees by societal and legal mechanisms already in place. Therefore, they sould receive separate and distinct consideration.
Once Superfund is split into its component parts, each part must be analyzed on its own merits. Does each part address a genuine need which requires enactment of new legislation?
With regard to spills of hazardous substances, there does not seem to be a demonstrated need for the sweeping superfund approach. Section 311 of the Clean Water Act and related sections of the law already provide an adequate mechanism for dealing with such spills.
Section 311 authorizes a $35 million fund to clean up and repair spill damage; penalties for violations; recovery of fund money from wrong-doers; and incentives for safe handling, prompt reporting and immediate cleanup. Further more, there is backup authority in Section 504 of the Clean Water Act. This section, which has never been funded, authorizes $10 million for the Adminis trator to prevent, limit or mitigate imminent or substantial danger to public health of welfare caused by the release into the environment of any pollutant.
Where new legislation is clearly needed, however, is in the area of old "orphan" dumpsites. These old sites create problems which are not feeing ade quately addressed by existing law. Congress should establish a Federal fund to provide for emergency assistance and containment in cases where orphan dunpsites are causing an imminent threat to public health and where no other party is taking responsible action.
C. Damages Covered
A further consideration is the specific types of damages a superfund should cover. One approach is to limit damages to cleanup and containment. Others would provide for restoration of natural resources, third party economic damages, personal injury, lost tax revenues and additional items.
CMA. has testified that the fund should be limited to emergency response and containment. This is based of the view that an extensive relief program could quickly exhaust the fund, especially if it covered third party claims without discrimination. IKLess the fund focuses on emergency cleanup and strict attention is given to prioritizing the use of fund monies, the fund could quickly mushroom out of control.
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D. Toxics Tort Law And "The Conrad Kent Proposal"
A key question is whether to create a new Federal toxic tort law to com pensate persons injured by toxics. CMA has strongly opposed this proposal on the grounds that tort liability is an area traditionally regulated by the states under our system of government. The Federal government should not usurp this responsibility by developing its own personal injury compensation system for hazardous substance spills and waste sites.
In lieu of a Federal toxic tort law, CMA supports creation of a Federal relief program to assist injured parties who might otherwise suffer economic hardship. This program would establish a $50 million fund which would promptly compensate those harmed by involuntary exposure to hazardous substances.
The intent is not to provide a make-whole remedy and give dollar-fordollar reimbursement for all damages. Instead it is meant to provide injured parties with immediate short-term relief so that they can make it through the injury without suffering economic hardship as a consequence. To achieve this goal compensation is limited to calculable out-of-pocket losses for certain types of damages, not necessarily in their full amount. Such conpensable losses would include out-of-pocket medical expenses, lost wages and the loss of repairing or restoring damaged property.
A claimant who receives compensation from the fund may still elect to sue the alleged wrongdoer under existing law. To cover the benefits paid on the private damage claim, the fund would have a lien on 80 percent of any amount recovered, net of costs and reasonable attorney's fees. The remaining 20 per cent would not be subject to the lien and would be retained by the claimant as an incentive to bring the suit.
The effect of the proposal is to avoid creation of a new Federal cause of action, not impose strict liability and to preserve the existing state tort law system. This proposal has previously been approved by CMA's Executive Committee, and is frequently referred to as "the Conrad Kent proposal". Mr. Kent is the Vice President - law of Stauffer Chemical Company and drafted the original language.
E. The "Release-Into-The-Environment" Concept
Another type of scope issue is the disturbing concept embodied in S. 1480 which,. in effect, prohibits any release into the environment. This concept, is a fundamental departure from current environmental law. S. 1480 sets aside the technology and health effects bases of the Clean Air Act, Clean Water Act and RCRA. Under this bill any discharge or emission -- even one carefully and specifically permitted under existing law -- would be subject to wide ranging and open-ended liability.
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CMA has strenuously opposed this far-reaching concept. Following is an excerpt from testimony by Frank Friedman (ARCQ) speaking on behalf of the Association.
"The bill (S. 1480) unjustifiably prohibits the release of any hazardous substance into the environment, thereby replacing the present and well-established system of regulating these substances on the bases of technology and danger to public health and the environment. It will conflict with, confuse, and duplicate ouch of the environmental legislation now on the books.
The all-encompassing prohibition on the release or disposal of any hazar dous substance would have the inevitable effect of overturning the entire basis of existing environmental legislation and regulations. This prohibition cuts across the gaunt of environmental, health and safety statutes, including the Clean Air Act, the Clean Water Act, RCRA, MPRSA, FIFKA, FDA, OSHA, and TSCA. These laws presently place specific limits upon releases into the environment based upon a careful assessment of . the danger to public health and welfare, -'the availability of control technology, and other factors. The bill would repeal limits on emissions and discharges that EPA has found to be adequate to protect public health and welfare, and would mean that billions of dollars invested by industry to comply with existing requirements will have been wasted.
It also would render unlawful that conduct which is now expressly per mitted under Federal and state programs. The blanket prohibition on any release provides no safe harbor for existing statutory systems. For example, releases in compliance with valid Federal and state water and air permits would subject the discharger to unlimited liability."
II. LIABILITY ISSUES
It is difficult to address the liability issue in the abstract. With out focusing on precise language of a given bill it is hard to assess the overall impact of a proposed liability scheme. For example, strict liability may be acceptable in some limited curcumstances. In combination with strict liability, however, other factors may pose such serious problems -- factors such as loose causation principles, broadly defined categpries of damages, and inadequate defenses. Despite these uncertainties, following are some general observations on liability issues in Superfund.
A. Joint and Several Inability
It is unfair and unwarranted to impose joint and several lianility for all consequences of a hazardous waste disposal incident. Imposition of such lia bility would mean that a person with a peripheral or even virtually nonexistent relationship to damages could be held responsible for all costs. Thus, a com pany with extensive assets responsible for disposing of one barrel of hazardous waste in a leaking site could be liable for all damages from 10,000 barrels in the same site. Making one party pay for the wrongs of all other persons is unjust and punitive. The modem concept of comparative responsibility -- which
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apportions liability based on the extent of responsibility -- should be sub stituted in its place. This concept has gained wide support in the state tort law reform movement.
B. Retroactive Liability And Proximate Cause
The retroactive change in liability principles is of major concern. Imposition of strict liability without allowing traditional defenses based on proper and reasonable conduct would require a person to unfairly bear liability. Proximate causation should also be required. Proximate cause limits recovery to those injuries which in fact resulted from the negligent act. The conduct in question mist be a substantial factor in bringing about the harm. Where it is not shown with reasonable certainty that the harm or loss resulted from the act complained of, there can be no recovery or compen satory damages.
C. Strict Liability For Cleanup Costs
Nevertheless, strict liability for only cleanup costs may be acceptable under certain circumstances. Provision of appropriate defenses is essential. Without safeguards, strict liability could become a heavy burden for even the largest companies.
Strict liability for other types of damages, however, is generally not acceptable. This is especially true in the case of private injuries. Per sonal injury liability is best left to the states, which historically have had jurisdiction over tort law.
D. Limits On liability
If a strict liability regime is established, there should be a limit on liability. Otherwise a company could be financially crippled by a single in cident even when it is not at fault. A mechanism which sets a nwxinum lia bility limit but allows establishment of a lower limit for certain classes or categories would seem appropriate.
E. Tort Law Vs. Welfare Relief Concept
There is a substantial difference between a welfare system and a tort law system. Welfare is the relief which society provides to parties who are in need or who have been injured and have no other source of relief. Tort law, however, is a system which provides relief to injured parties by means of assigning responsibility and accountability to some other individual or institution in society. Society itself does not pay for the relief provided by the tort law system. Instead, relief flows from party to party on the basis of a determination of legal responsibility.
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The distinction between a welfare system and a tort law system should be maintained rather than blurred by loose tort law concepts. Private en tities should not be called upon to fund a welfare system. Welfare is a societal responsibility, or at least a responsibility discharged by private entities on a voluntary basis. CMA. is willing to support responsible and well-tailored welfare legislation for persons harmed by exposure to hazardous substances, such as the previously discussed "Ccnrad Kent proposal."
F. Liability Guidelines
To surnnarize the discussion .on liability issues, a wise policy would seem to be as follows:
- oppose joint and several liability, support a system of comparative responsiblity;
- consider accepting strict liability for cleanup costs only but maintain adequate defenses;
- leave personal injury and third party liability issues to state tort law;
- insist upon tight causation principles; and
- establish liability limits.
III. FUNDING ISSUES
Who should be responsible for providing funds for any superfund? Three approached are now under consideration: public funding, industry fees or some combination of the two.
A. Public Funding
CMk has argued strongly in fa\or of public funding for the following reasons.
First, the hazardous waste problem is societal in nature and only through the use of public monies can this societal responsiblity be fairly discharged. Hazardous wastes are an integral by-product of our industrial society. They have been and will continue to be generated by a wide range of industries, busi ness concerns, government agencies and defense installations, municipalities and scientific facilities.
Second, it is unfair to single out the chemical industry for punishment through a fee system. The EPA has itself identified 17 major industries which generate large amounts of hazardous waste.
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Third, today's companies should not have to pay for practices of yester day's industrial producers.
Fourth, inposition of a fee to pay for orphan dumpsites raises serious constitutional questions under the due process clause of the Fifth Amendment.
Fifth, off-budget financing through a fee on industry is an irresponsible way to launch a new Federal program that otherwise would not make the grade. Such financing hides appropriation of societal funds from the public and shields the program from the normal scrutiny of the budget process. The off-budget financing precedent is a most important argument against an industry fee, as indicated in the attached excerpts from a recent speech by Edmund B. Frost, CMA Vice President and General Counsel, before the API/NFPA Environmental Form VIII.
"The real reasons for placing the fee on industry emerges when we turn to budget considerations. Some staffers on the Hill have been quite candid in admitting that they want an industry fee simply because the normal and orderly budgetary processes will not rank Superfund sufficiently high to allow it to be funded. Their alternative is a fee system or "off-budget financing." This hides appropriation of societal funds from the public and from the normal scru tiny of the budget process.
At first blush, this is an attractive way to fund a new program which cannot otherwise cut the mustard. But while off-budget financing may be a good way to launch a new program without full public scrutiny, it is not a good way in the long run for the Federal government to control its use of our society's resources. In terms of fiscal policy and inflation, a fee levied on the chemical industry would have essentially the same effect as a tax. And, in addition, the use of that fee in a superfund would be the same as a Congressional appropriation. But regular fiscal and budgetary controls would lapse. Control of inflation, however, depends on the ability to control and balance the govern mental sector. From an inflation point of view and as a precedent for financing new programs, the industry fee concept is terrible, if not irresponsible."
Sixth, with regard to spills of hazardous substances, existing legal mecha nisms such as the Clean Water Act and state tort law satisfactorily provide for recovery of damages.
B. Industry Fees
Nevertheless, serious consideration is being given on Capitol Hill to the imposition of an industry fee. A major reason is budgetary -- many pro ponents of Superfund want an industy fee because they believe that fiscal and budgetary priorities and constraints would not permit the massive and immediate amounts of monies they envision.
The two fee mechanisms most frequently discussed are a front-end feedstock fee and a back-end disposal fee.
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1. THE FRONT-END APPROACH derives money from producers of hazard ous1 materials by assessing a per unit fee on oil, petro-chemical feedstock and certain other inorganic chemicals and heavy metals. The major advantage cited by its proponents is that this type of fee is easy to administer. There are numerous disadvantages, however.
First, it penalizes companies that have over the years adequately managed their waste disposal problems.
Second, the hazardous waste disposal site problem is not the result of the production of hazardous substances. The real problem is unproper disposal of hazardous wastes.
Third, a feedstocks fee places a burden on products that do not ultimately generate hazardous waste. Some products that do not generate hazardous waste would nevertheless be taxed heavily.
Fourth, the fee is not so easily passed down the chain as some would argue. The chemical industry is highly conpetitive.
2. THE BACK-END APPROACH derives money through a tax or fee on the disposal of hazardous waste. An advantage is that the charge is more closely related to the problem of hazardous waste disposal. Moreover, it is consistent with RCRA in that it encourages recycling and recovery of hazardous waste. Also it encourages the reduction of the amount of hazardous waste disposed. It could also be structured to place the highest burden on the most dangerous wastes.
However, there are some major disadvantages.
First, a disposal fee system would be difficult to administer because of the higfr number of fee collection points.
Second, there is a danger that generators of high volume/low toxicity wastes could be required to pay an undue share of any fee.
Third, a related problem is that a large volume of waste is water-based. It would distort the fee if water is included.
Fourth, the disposal fee wculd raise costs of legal disposal and might thereby encourage midnight dumping.
Fifth, this fee mechanism likewise penalizes companies that have over the years adequately managed their wastes.
C. Fees And The Release Concept Of S. 1480
Older the Culver-Muskie bill, S. 1480, companies would be subject to very substantial environmental fees even though they are complying with existing laws and even though their releases cannot be shown to result in injury or damage.
CMA 062647
-9The bill inposes substantial fees on the production of hazardous sub stances and on the generation and release of hazardous substances from any factory, vessel of motor vehicle even if the person manufacturing or releasing the substance was in full compliance with the requirements of other federal environmental laws. Under the extremely broad coverage of the bill, a hazardous substance is one which would adversely affect any organism, and a release is any accidental or intentional emission, discharge, or other release of such a substance into the environment. Thus, a facility discharging any amount of a hazardous substance in accordance with an NPDES permit, emitting any amount of a hazardous substance in compliance with the Clean Air Act, disposing a hazardous waste im compliance with RCRA, or otherwise releasing into the environment any amount of a substance which might adversely affect any living organism would be liable for the payment of fees on the basis of each such release. The proponents of the bill expressly intend that the fees be universally applicable to all releases and set at such amounts as to encourage the use and development of "technology to eliminate all releases or at least to reduce such releases substantially below the levels permitted under existing law.
CMA 062648
Exhibit C
CHEMICAL INDUSTRY COMMUNICATIONS/PUBLIC SUPPORT PLAN
The CMA Executive Committee and Board of Directors, meeting in New York City on November 19, approved in principle the chemical industry's Communications/Public Support Plan subject to a final decision on January 7. At the same time, the Board recommended that all member companies be thoroughly informed once again as to the objectives, scope and content of the program* Accordingly, CMA on December 3 distributed a complete packet of information on the plan, the industry's public attitude problems and the role of the new Science Advisory Group. Therefore, since all Executive Contacts have already received this documentation, we in clude here only an Executive Summary of the plan,, plus the particular pages that deal with budget and funding.
Action Requested: Approval of the Plan
CMA EC-1/7/80 BD- 1/8/80
CMA 062649
COMMUNICATIONS/PUBLIC SUPPORT PLAN
EXECUTIVE SUMMARY
1. It is evident that public concern is growing about the dangers of chemicals in products, the environment and the workplace and a perceived failure of industry to do enough to manage these risks.
Surveys show that the chemical industry rates very low in public favorability. Other surveys rate the industry as doing the "poorest job" in complying with air and water pollution laws, and as not doing enough to reduce risks.
These negative attitudes are bolstered by increased news media coverage of environmental attitudes and by the activities of environmentalists. These attitudes appear to be even more negative among government officials, with irrational and poorly conceived legislation and regulation often the result.
2. The implications to the industry of such attitudes are massive in terms of compliance costs and impaired business. Innovation and product development suffer, plant construction lags because of community resistance and the investment community puts its funds elsewhere.
3. A major, long-term effort is needed to communicate industry's efforts and to build a more balanced perspective in the public's mind about chemicals and the chemical industry. The most logical means of mounting such an extensive, lengthy program is through a joint effort by all CMA members that would lessen the burden on any one company.
4. Primary message objective: To increase recognition that the chemical industry is committed to doing a responsible job to protect the public from the health and safety risks of chemicals -- specifically in the major concern areas of air and water pollution, product safety, transportation safety, worker safety and hazardous waste disposal. The story of industry essentiality and benefits would be incorporated as a basic part of this objective.
The audience objective: The first stage includes political actives, government officials, communicators, academics and the public in areas of major plant concentrations. The second stage would expand the audience to include more of the general public, assuming that testing and research determines such an expansion to be desirable.
CMA 062650
5. All appropriate communications tools will be used, including a full range of news media activity and establishment of an Information Monitoring and Response System to spot and refute inaccurate statements. A Science Advisory Group will provide authoritative voices where appropriate, and a speakers program will extend impact on both the national and community levels. Publications and films will be used, while advertising will be used to provide control over content and timing of the program's message and to target this through key publications.
6. A key aspect of the program will be encouragement of individual company use of materials at the local and company level. Such grassroots activity is essential to effecting changes in public opinion or in public policy. Companies will be kept fully informed on the progress of the program by timely reports that will include results of continual research on effectiveness.
7. Funding of the program will be by a special assessment based on the traditional formula followed to establish member's dues.
8. Timing of the program: This includes an expanded public relations effort that has already begun, with production of booklets and Speakers Kit, News Media Tours and other projects accelerating in January. The advertising program is scheduled to begin in early 1980.
CMA 062651
BUDGET
The following estimates have been developed by the Task Force as a general guide to financial requirements. It should be underscored that the advertising budget figure for the June 1, 1980 - May 31, 1981, period does not include funds for expansion of the advertising program to a major share of the general public during this time frame. Such a program and budget will be determined upon completion of expenditure level tests for the general public which are scheduled to be undertaken in the first half of 1980.
June 1, 1979 - May 31, 1980
Advertising Expenditure Level Test P.R. Agency Fee, out-of-pocket Publications/Films Tracking Research Internal Staff Addition Reserve
($ '000s)
1 ,500 400 225 150 110 70 100
2,555
June 1, 1980 - May 1981
Advertising P.R. Agency Fee, out-of-pocket Tracking Research Internal Staff Addition Publications/Films Reserve
3,000 225 100 100 75 100
3,600
CMA 062652
FUNDING
It is the Task Force's recommendation that funding for the program be generated by a special assessment to all member companies, at least during the first two years of the program (June 1, 1979 - May 31, 1980).
The special assessment would be based on the same formula as member dues: i.e., per cent of applicable salis.
Shown below are estimated assessment figures for member companies for the first and second years of the program.
For Companies with Chemical Sales of:
$1.0 million 50 million
100 million 400 million Over 400 million
First Year Assessment
$1,539 4,626 7,704
27,648 Up to maximum of 86,580
Second Year
$2,137 6,425
10,700 38,400 Up to maximum of 120,250
CMA 062653
Exhibit D
LABELING ISSUES
Federal mandatory hazard warnings and chemical ingredient disclosure will be among the first and most important issues to confront industry in 1980. Labeling is already the subject of litigation and, early in 1980, is scheduled to be the subject of complimentary rulemaking proposals by both EPA and OSHA.
These federal labeling initiatives will involve sensitive and complicated issues. As merely three examples, industry will be faced with such questions as:
(a) how and when should the federal government require that substances which are or may be carcinogenic to animals be labeled in the workplace; in commerce in general?
(b) when do health and safety considera tions justify disclosure of the identi ty of the confidential ingredients of chemical products?
(c) should the federal government require that every chemical be labeled as to its full ingredient composition and as to its actual or potential adverse effects regardless of the severity of those effects?
Federal labeling rules are a concern which is rapidly maturing at this time for several reasons. In general, labor unions and environmentalists have begun pushing EPA and OSHA to expedite publication of labeling proposals which would violate or conflict with the agencies' respective statutes. Furthermore, Congressional interest has begun to focus upon the issue of workers' "right to know" of the health consequences of materials with which they are working. However, as is so often the case in health and safety matters, the Congressional rhetoric is developing in a fashion which promises to emphasize emotion of purpose over precision of thought.
Labor unions and environmentalists have been strongly urging EPA and OSHA, verbally and in writing, to propose coordinated labeling rules before the end of 1979 which would mandate labeling of large generic
CMA 062654
2- -
categories of substances suspected of posing any of a wide range of actual or potential effects, and to mandate full disclosure of all of the ingredients of all chemical products. In September the Public Citizen Health Research Group, the Philadelphia Area Project on Occupational Safety and Health, and U.S. Congressman Andrew Maguire (D-NJ) filed suit in the District Court for the District of Columbia seeking to compel OSHA to promulgate a rule requiring employers to "apprise employees and employee representatives of the identity of all potentially toxic materials and harmful physical agents to which they may be or may have been exposed in the workplace."
CMA has intervened in that litigation against the plaintiffs arguing that Congress gave OSHA labeling authority in connection with substances for which the agency had promulgated a standard, not omnibus authority for generic labeling and disclosure requirements.*
When CMA learned that-EPA's staff efforts to develop a labeling rule promised to take that Agency outside its statutory authority as well, it directed outside counsel to submit a letter to Administrator Costle (and EPA staffers, with copies to Eula Bingham and interested OSHA staffers) carefully detailing CMA's view of EPA's statutory labeling authority.**
At the present time, CMA is continuing to communicate with both agencies. However, it appears to be very likely that the labor and environmentalist constituencies which are pushing the agencies into labeling rules will succeed in convincing the agencies to propose rules which in signi ficant part will be unnecessary, counterproductive, burden some and beyond their respective mandates. Nevertheless, the regulatory and litigation battles will be difficult and laden with the current red flag issues of our industry -- cancer, confidentiality, the workers' "right to know," generic rulemaking versus case by case rulemaking, and the issues of the cost burdens imposed by health and safety regulations.
In Congress these same red flag issues will be surfacing not just in regard to labeling but in the broader context of industry responsibility in the health and safety area.
For instance. Congressman Edward P. Beard (D-RI) as chairman of the House Subcommittee on Labor Standards held hearings last spring concerning compensation for occupational
CMA 062655
-3disease issues. He has indicated that as a result of those hearings one of the things he has become convinced of is that there does not exist adequate labeling on substances in the workplace.
Expanded criminal penalties are being proposed in two very active pieces of legislation which will serve to focus on industry's health and safety activities. The so-called Miller Bill (H.R. 4973) would impose criminal penalties on corporate officials who knowingly fail to inform their employees and the government after discovering a serious danger of death or serious bodily injury associated with a product or business practice. In addition, the latest draft of revisions of the federal criminal code provides criminal penalties for persons who knowingly engage in con duct which places another in imminent danger. Both of these bills reflect Congress' expanding interest in corporate criminal responsibility and the certainty that health and safety issues will receive more rather than less attention.
This report is for information only. No action required.* **
* Memorandum of Points and Authorities In Support of Motion of Chemical Manufacturers Association for Leave to Intervene as Defendant attached.
** October 26, 1979 letter to Douglas Costle re Labeling Regulations for Industrial Chemicals Under TSCA attached.
CMA 062656
IN THE
UNITED STATES DISTRICT COURT FOR THE DISTRICT OF COLUMBIA
PUBLIC CITIZEN HEALTH RESEARCH GROUP 2000 P Street, N.W. Washington, D.C. 20036
PHILADELPHIA AREA PROJECT ON OCCUPATIONAL SAFETY AND HEALTH
1321 Arch Street Room 201 Philadelphia, Pa. 19107
and
UNITED STATES CONGRESSMAN
ANDREW MAGUIRE
1314 Longworth House Office
Building
Washington, D.C.
20515
Plaintiffs,
v.
RAY MARSHALL, Secretary
United States Department of Labor
Third Street & Constitution
Avenue, N.W.
Washington, D.C.
20210
Defendant,
CHEMICAL MANUFACTURERS ASSOCIATION
1825 Connecticut Avenue, N.W.
Washington, D.C.
20009
Applicant for Intervention.
)
) ) )
)
) ) ) ) )
) )
)
) ) ) ) )
) )
) )
) ) ) ) ) )
) )
)
)
) )
) )
)
Civil Action No. 79-2581
MEMORANDUM OF POINTS AND AUTHORITIES IN SUPPORT OF MOTION OF
CHEMICAL MANUFACTURERS ASSOCIATION FOR LEAVE TO INTERVENE AS DEFENDANT
In support of its Motion for Leave to Intervene
as Defendant, the Chemical Manufacturers Association (CMA)
respectfully states as follows:
CMA 062657
X. Intervention as of Right Is Warranted. A. The Motion Is Timely.
CMA's motion to intervene is being filed less than
three weeks after the filing of plaintiffs' complaint. While
the time elapsed from the beginning of this litigation is not V
the sole test, it is reasonable to say that a motion for
leave to intervene filed so soon after the filing of the
complaint will not unduly delay the proceeding. That is
particularly true in this case where an answer has not yet been filed and defendant has 60 days (or until November 26,
1979) to answer. B. CMA Meets the Requirements for Intervention as of Right.--____________________________________
In Nuesse v. Camp, 128 U.S. App. D.C. 172, 38S
F. 2d 694 (1967) , our Court of Appeals summarized the require
ments for intervention as of right under Fed. R. Civ. P. Rule
-24(a)(2) as follows: "(i) an interest in the transaction, (ii) which the applicant may be im peded in protecting because of the action, (iii) that is not adequately represented by others." (128 tJ.S. App. D.C. at 177, 385 F.2d at 699).
CMA satisfies each of those requirements.
1. CMA's interest in the transaction
CMA's member companies produce more than 90% of this country's basic chemicals. Many of these chemicals
may be considered as potentially toxic materials or harmful physical agents. A considerable number are now regulated
by occupational safety and health standards (derived from
national consensus standards) promulgated under section 6(a)
*/ Hodgson v. United Mine Workers of America, 153 U.S. App. D.C. 407, 418, 473 F.2d 118, 129 (1972)"
CMA 062658
2
of the Occupational Safety and Health Act of 1970, 29 U.S.C. 5 655(a) (the OSH Act). A smaller number are regulated by new or amended occupational safety and health standards promulgated pursuant to section 6(b)(S) of the OSH Act, 29 U.S.C. S 655(b)(5).
Plaintiffs have requested that the Court issue an order "(1) directing the defendant to take action forthwith on plaintiffs' petition for rulemaking ... (2) directing defendant forthwith under sections 6(b) (7) , 8(c) (1) and 3(c)(3) of the OSH Act, 29 U.S.C. 655 (b)(7), 657(c) (2)[sicJ and 657(c)(3), rules requiring employers to apprise employees and employee representatives of the identity of all potentially toxic materials and harmful physical agents to which they may be or may have been exposed in the workplace, (3) retaining jurisdiction over this action to insure that there is no unreasonable delay by defendant in completing the rulemaking proceedings, ..." and for other relief. (Complaint, pp. 6-7, emphasis supplied).
Since plaintiffs have requested an order compelling immediate action by the defendant, it is probable that plain tiffs. and defendant will submit to this Court for its approval an agreement establishing time limits for proposing a regula-
y tied and for the ultimate promulgation of that regulation." CMA has a direct interest in the subject matter of the regu lations and in being a party to the rulemaking from its outset.
See,
20588 (June Agreement).
N.H.D.C. V. Train, 8 E.R.C. 2120, 6 E.L.R. . (Final Order and Decree, and Settlement
3
CMA 062659
2. Denial of intervention may impede CMA in protecting its interest. If the present parties submit an agreement
for approval of the Court establishing the time limits of proposed regulation, CMA's ability to protect its interests and the interests of its member companies may be signifi cantly impaired. It is not enough that CMA may have a later opportunity to participate in rulemaking proceedings before the agency or to seek review of final agency action. As our Court of Appeals said in Natural Resources Defense Council v. Costle, 183 U.S. App. D.C. 11, 561 F.2d 904 (1977) :
"Judicial review of regulations after promulgation may, 'as a practical matter', afford much less protection than the opportunity to participate in post settlement proceedings that seek to ensure sustainable regulations in the first place, with no need for judicial review." (183 U.S. App. D.C. at 16, 561 F.2d at 909). While the situation in that case involved motions to inter vene after a Settlement Agreement had been reached, the Cour-t's statement is of equal force here. An opportunity to participate in pre-settlement proceedings may also help in producing regulations which are reasonable in scope and timing and nut the result of "precipitous actions which ultimately lead to further and additional litigation to set aside regula tions so developed in hurried fashion without adequate factual foundation or analysis." (National Resources Defense Council v. Costle, supra, 183 U.S. App. D.C. at 17, 561 F.2d at 910).
CAM 062660
3. CMA's interest will not adequately be protectad by existing parties.
Plaintiffs in this proceeding are the Public
Citizen Health Research Group, the Philadelphia Area Project
on Occupational Safety and Health, and United States Congress
man Andrew Maguire. These plaintiffs seek immediate promul
gation of proposed regulations. CMA believes that, such imme
diacy may lead to the proposal of unreasonable regulations
and even of regulations beyond the authority of defendant to
issue. CMA's interest will not be protected by the plaintiff
parties.
Furthermore, the interests of CMA and defendant
y
"may not coincide" in all respects.
Thus, CMA understands
that plaintiffs seek regulations which would require disclo
sure to employees and to employee representatives either by
labeling or other means, of the identity of all toxic mate
rials or other harmful physical agents to which employees
may be or may have been exposed in the workplace. CMA be
lieves that such an all-encompassing regulation is beyond
the authority delegated to the defendant in sections 6(b)(7),
8(c)(1) and 8(c)(3) of the OSH Act, 29 CJ.S.C. 5 635 (b)(7), **/
557(c)(1) and 657(c)(3).
Since agencies are generally
*/ National Resources Defense Council v. Costle, supra, X83 U.S. App.D.C. at 19, 561 F.2d at 912 (citing Nuesse v. Camp, supra, 128 U.S. App. D.C. at 181, 385 (F.2d at 703).
**/ For example, section 6(b)(7) of the OSH Act, 29 CJ.S.C. S 655(b)(7) provides:
"Any standard promulgated under this subsection shall prescribe the use of labels or other appro priate forms of warning as are necessary to insure that employees are apprised of all hazards to which they are exposed, relevant symptoms and appro priate emergency treatment, and proper conditions and precautions of safe use or exposure." (Emphasis added).
[Footnote continued on following page]
5 CMA 062661
reluctant to admit the limitations of their statutory
authority, it is unlikely that defendant will raise the
issue, and thus CMA's interests will not be protected by
defendant.
C. Conclusion
tn view of the foregoing, CMA submits that it
satisfies the requirements of Fed. R. Civ. P. Rule 24(a)(2)
and should be granted leave to intervene as defendant as
of right.
II. In the Alternative, CMA Should Se Granted Permissive Leave to Intervene.
Rule 24(b)(2) provides that any person may be
granted leave to intervene when his claim or defense and
the main action have a question of law or fact in common
and when intervention will not unduly delay or prejudice
the adjudication of the rights of the original parties.
CMA submits that the discussion above establishes
that its defense has questions of law and fact in common
with the main action, and that intervention should be per
mitted because of the interests CMA has shown. Also, inter
vention by CMA will not cause undue delay. The motion for
leave to intervene is being filed less than three weeks after
the filing of the complaint, and about six weeks before the
defendants' answer is due.
[Footnote continued]
The requirement of labels or other appropriate forms of warn ing is thus limited to cases where standards have been promul gated under section 6(b)(5) of the OSH Act, 29 U.S.C. * 655(b) (5), and does not extend to standards promulgated under section 6(a) of that Act, 29 Cf.S.C. 5 655(a). Relatively few toxic substances are subject to standards aromulaated under section 5(b)(5). See 29 C.F.R. 3 1910.1001-1910.1046. The great majority of toxic substances are subject to standards promul gated under section 5(a). See 29 C.F.R. s 1910.1000, Tables 2-1, 2-2 and Z-3. See also 39 Fed. Reg. 23502, 23540-43 (1974), recodified at 40 Fed. Reg. 23072-73 (1975).
CMA 062662 6
CONCLUSION For the reasons stated herein and in the accompany ing motion, CMA should be granted leave to intervene as of right or, alternatively, should be permitted to intervene in this action.
Respectfully submitted,
John H. Pickering t
October 17, 1979
Andrew T.A. Macdonald
WILMER & PICKERING 1666 K Street, N.W. Washington, D.C. 20006 (202) 872-6000
Attorneys for Chemical Manufacturers Association
7
CMA 062663
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October 26, 1979
t'
The Honorable Douglas M. Costle Administrator U.S. Environmental Protection Agency ' 401 m Street, S.W. * Washington, D.C. 20460
Re: Labeling Regulations for Industrial Chemicals Under TSCA
Dear Mr. Costle:
! This firm represents the Chemical Manufacturers [ Association (CMA), a trade association whose member companies
account for more than 90 percent of the total production It capacity for basic industrial chemicals in the United States, f w are writing about an issue of great concern to the chemical 1 industry -- the promulgation of hazard-related labeling > requirements for industrial chemicals under the Toxic Sub
stances Control Act (TSCA). According to recent press accounts, the Environmental Protection Agency (EPA) and the
Ji Occupational Safety and Health Administration (0SHA) are now proceeding with a joint program to develop such labeling [ requirements and intend to publish proposed rules on the sub| ject in the next few months.
\ CMA1s members are committed to providing their { employees and customers with adequate information concarn| ing the safe use of chemicals. Together with its member
1 companies, CMA has participated actively in developing and i implementing voluntary labeling programs to achieve this
objective. 3ased on its expertise and experience, CMA stands ready to assist EPA in developing labeling regu| lations under TSCA which have similar aims. Indeed, CMA
f has already offered such assistance to the Agency in a letter
CMA 062664
CVInGTON S 3U3LING
The Honorable Douglas M. Castle October 26, 1979 Page Two
dated July 6, 1979 which was addressed jointly to you and Dr. Bingham of OSHA.
At the same time, CMA strongly believes that any labeling requirements which EPA adopts must comport fully with the requirements of TSCA. Recent press accounts of public statements by certain EPA officials indicate that, in it3 current deliberations, the Agency may not be devoting sufficient attention to applicable statutory provisions* Accordingly, before the rulemaking process progresses any further, we wish to direct ZPA's attention to certain basic principles, derived from the text and legislative history of TSCA, to which any EPA labeling proposal must conform. These principles, we believe, provide the basic framework within which EPA's labeling rules must be developed.
1. Definition of Unreasonable Risk
The central issue which any labeling proposal must address is the criteria for imposing labeling requirements. EPA must develop principles for determining which chemicals will be labeled, which manufacturers and processors of those chemicals will be subject to labeling requirements, and what level of risk must be presented before those labeling require ments come into play.
In examining these questions, EPA must be guided by Section S(a) of TSCA, from which the Agency's authority co require labeling derives. Gnder Section 6(a)(3), EPA may promulgate rules directing that a substance or mixture "be marked with or accompanied by clear and adequate warnings and instructions with respect to its use, distribution and com merce, or disposal ..." As specified by Section 6(a), the precondition for imposing such requirements is a finding that "there is a reasonable basis to conclude" that the chemical substance or mixture in question presents or will present "an unreasonable risk of injury to health or the environment." In decarmining whether such a risk exists, EPA must be guided by Section 6(c) , which requires it to consider, and publish a statement with respect co, four factors before promulgating a rule under Section 5(a): che effects of the chemical on health and the er.vironmenc, the magnitude of human and environmental exposure co Che chemical, che chemical's benefits for various uses and che availability of substitutes for Chose uses, and che probable economic effect of EPA'3 proposed action, in cluding it3 impact on small business and technological
CMA 062665
COVIN jTON 5 BURLING
The Honorable Douglas M. Castle October 26, 1979 Page Three
innovation. Thus, EPA must weigh the potential harm associated with the specific chemical against the adverse economic and social impact of regulatory requirements.
These provisions have a number of important impli cations for any labeling rules which EPA adoots under Section 6(a)(3).
First, EPA cannot promulgate labeling requirements for a chemical which, under its actual conditions of use and exposure, poses no risk or a risk that is insubstantial. Rather, the statute requires a finding of "unreasonable risk" as a prerequisite to. labeling requirements. Thus, EPA must make some showing that, absent labeling instructions concern ing safe use of a chemical, that chemical will cause signifi cant harm to humans, the environment or both. EPA is not em powered to require labeling information which relates to hazards which are purely theoretical or to hazards which, in view of a chemical's uses and exposure, are remote and of little prac tical concern. Moreover, since the concept of "unreasonable risk" involves a balancing of costs and benefits, the Agency must show that, for the chemical in question, the harm which labeling will prevent outweighs the expense and effort that labeling requirements will entail. If labeling a particular chemical will provide small benefits and impose large burdens, EPA cannot require that labeling under Section 6.
There is an important corollary to these principles which must shape the procedures that EPA utilizes to determine whether there is an "unreasonable risk" for which labeling can be required. Because risk is a function of the properties, uses and exposure patterns associated with a particular chemi cal, EPA cannot adopt omnibus labeling requirements which ap ply to a broad and non-specific chemical class. Rather, the Agency must present evidence concerning the alleged risks of each chemical proposed for labeling requirements, and industry must have a meaningful opportunity to comment on that evidence and respond with evidence of its own. With out a procedure which provides for these factual determinations concerning specific chemicals, the careful balancing test which underlies the Congressional concept of "unreasonable risk" could not be applied, and EPA's labeling requirements would be legally defective.
CMA 062666
he Honorable Douglas M. Costle October 26, 1979 Page Four
While an omnibus proceeding covering all or most industrial chemicals would be beyond EPA's statutory authoricy, a two-stage approach to developing labeling rules could be utilised that would satisfy statutory requirements. Dur ing the first stage of this process, EPA could develop a "prototype" labeling rule which (1) defines the different types and degrees of hazard which would trigger labeling obligations, and (2) for each such hazard, prescribes appro priate warnings and instructions and specifies methods for their dissemination. Once EPA has established the basic standards and procedures for labeling requirements, the Agency would then apply these standards and procedures to particular chemicals. This task would necessarily entail separate rulemaking proceedings for particular chemicals and, where appro priate, for chemical categories which are sufficiently narrow to satisfy Section 26(c) of TSCA. The focus of such proceed ings would be on whether the basic statutory criterion of "unreasonable risk" ha,s been met for a particular chemical in view of that chemical'3 specific properties, uses and exposure.
CMA would be willing to work with EPA in develop ing an appropriate "prototype" labeling rule under Section 6. It believes that the existing standard of the American National Standards Institute (ANSI) provides a useful point of de parture for acute hazard labeling and could be restructured tc embody the statutory concept of "unreasonable risk." It must be clearly understood, however, that such a rule would merely serve as a "model" for subsequent proceedings,- and these later proceedings would provide for a full considera tion of the unique facts which relate to individual chemicals.
2. The Importance of Minimizing Regulatory Burdens
Complemented by Section 2 of TSCA, Section 6 directs EPA to act prudently and responsibly, with constant and careful attention to the economic consequences of its regulatory decisions. Rules which EPA issues under Section 6(a) must prescribe the "least burdensome requirements" possible, while Section 6(c) directs SPA to make findings concerning the "reasonably ascertainable economic consequences" of any rule chan it proposes to adopc. Similarly, Seczion 2(b) (3) of the Act direcos EPA to exercise its authority "in such a manner as cot to impede -unduly or craace unnecessay economic barriers co oachnological innovation." Sec tion 2(c) amplifies this policy by providing that it is
CMA 062667
The Honorable Douglas M. Costle October 26, 1979 Page Five
"the intent of Congress that [EPA] shall carry out this Act in a reasonable and prudent manner" and by directing EPA to "consider the environmental, economic, and social impact of any action the Administrator takes or proposes to take under this Act."
These statutory provisions must be brought to bear on any labeling program which EPA proposes. First, the Agency must devote careful consideration to -- and attempt to minimize -- the potentially massive costs of making de tailed labeling information available at nearly every level of a chemical's distribution process, including its sites of manufacture, processing and disposal. If there are alternative communications tools which can minimize these costs and lessen the overall burden of compliance without jeopardizing the goals of the Agency's labeling effort, these alternative tools must form the basis of any EPA rule under Section 6(a)(3).
Equally important, EPA has a responsibility to avoid labeling requirements which place an unwarranted stigma on particular chemicals by exaggerating or misrepresenting the potential risks which they pose. Far this reason, every effort must be made to utilize a labeling terminology and format which accurately convey the severity and likelihood of any injury which particular chemicals can cause.
The need for a balanced presentation of potential risks is particularly great with respect to "chronic" hazards like carcinogenicity, mutagenicity and teratogenicity. In designing labeling requirements, EPA must taka into account the substantial scientific uncertainty involved in identify ing chemicals which can cause these effects. It must also take into account the disparate levels of risk which different chemicals pose depending on such factors as their innate properties, potency, uses and conditions of exposure. Signi ficantly, in its recent policy concerning the regulation of chemical carcinogens, the Regulatory Council stressed the importance of these considerations, indicating that any analysis of a substance's carcinogenic potential involves a "characterization of the extent and quality of the evidence supporting this determination" and an assessment of "the size of the exposed population", "exposure sources, routes, and conditions, the duration, frequency and intensity of exposure, and the relevant characteristics (e.g., age, sex, health) of
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the exposed population." 44 Fed. Reg. 50033, 50040 (October 17, 1379). Any SPA labeling program under TSCA which does not convey information concerning these matters would be incomplete and misleading.
EPA's goal should be to encourage informed and balanced decisions about chemicals by manufacturers, dis tributors, processors and workers. An approach which fails to place potential risks in proper perspective and causes undue alarm and disruption among users of chemicals would constitute poor public policy, discriminatory agency action and a violation of the requirements of TSCA.
3. Disclosure of Chemical Composition
Over the past several months, some groups have apparently advocated requiring all manufacturers and distrib utors of chemicals covered by TSCA to disclose the precise composition of those chemicals to their users, including exposed members of the workforce. In the case of "substances", this disclosure would involve the specific identity of the chemical. In the case of "mixtures", disclosure would involve listing the constituent substances of the chemical and the relative quantities in which those substances are present.
TSCA does not authorize EPA to require such an across-the-board disclosure of chemical composition. Under Section 5(a)(3), the Agency may require manufacturers and distributors to provide labeling information for one purpose only -- to afford protection against "unreasonable risks" within the meaning of Section 6 (a). In view of this purpose, EPA cannot require the routine disclosure of chemical composi tion for all chemicals. Rather, such disclosure can only occur on a selective basis ar.d must be tied to a determination that (1) the chemical in question presents an "unreasonable risk", and (2) that risk can be reduced or eliminated if users of the chemical are informed of its precise composition. The situations where this test is satisfied will be the infrequent exception, not the norm.
4. Confidentialitv
Any labeling program which raquiras the disclosure of chemical composition must also provide full protection for
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confidential business information. Frequently, the specific identity of a substance or the precise contents of a mixture is a valuable "trade secret" whose disclosure will enable competitiors to market products with identical properties and characteristics. In this situation, it is common for manufacturers to describe the chemical to customers and users
Iin "generic" terms and to withhold more precise information
I about its composition in order to prevent competitive harm.
I Under Section 14 of TSCA and 18 U.S.C, 1905, EPA has no authority to compel departures from this customary
Iindustry practice. Section 14(a) forbids EPA, except in c rtain limited circumstances, from disclosing information that I falls within Exemption 4 of the Freedom of Information Act, I 5 U.S.C. 552(b)(4). This exemption applies to "trade secrets * and commercial or confidential information obtained from a r person and privileged or confidential." Similar obligations
are placed on EPA by 18 U.S.C. 1905, which requires all federal agencies to safeguard trade secrets. Section 14(b) creates a narrow exemption from EPA's duty to withhold com-, petitively sensitive information for "any health and safety study" submitted to the Agency. Clearly, however, labeling ; information covered by a Section 6(a)(3) rule could not be r considered part of a "health and safety study." Moreover, j Section 14(b) does not permit EPA to compel disclosure of * confidential procedures used in manufacturing or processing f a chemical or the portion of a mixture comprised by its com ponent chemical substances. Much of the information concern' ing chemical composition which EPA's labeling rules might encompass would clearly fall in this category. This informa tion would still be immune from disclosure even if Section 14 (b)'s exemption for "health and safety studies" were to apply.
It is true that Section 14(a) (4) permits EPA to . require the disclosure of confidential commercial information ' when "necessary to protect health or the environment against I an unreasonable risk of injury ..." CMA questions, however, . whether the disclosure of precise information concerning
chemical composition will ever be "necessary" within the | meaning of this provision. Instructions concerning proper 1 use and handling of a chemical, augmented by a "generic" , description of its composition, will be sufficient to enable | the chemical's users to protect exposed persons. For this f reason, a more precise description of the chemical's identity
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would not add to the goal of safe chemical use. Since an I adequate labeling program can be developed without dis
closing the precise composition of the chemicals it covers, SPA has no authority under TSCA to require such disclosure where it would compromise the protection of trade secret information.
*
The above principles provide a necessary legal framework for any labeling program which EPA proposes under Section- 6- of--TSCA, If the Agency conforms to- these-*-prin--------ciples, we believe that it can develop a labeling proposal which is constructive, affective and in keeping with statu tory requirements. Within the basic legal framework outlined in this letter, CMA stands ready to assist the Agency in formulating the particulars of such a labeling proposal. The undersigned and other CMA representatives would be happy to discuss thi3 matter further with you or your staff on a mutually convenient data.
In conclusion, we wish to emphasize that any industry-wide labeling program that EPA adopts would be a massive undertaking which involves substantial cost and effort by industry and significant long-term effects on the attitudes of those who make and use chemicals. Any program of this scope and impact deserves the most careful consider ation by ail concerned.
cc: Dr. Suia Bingham Steven Jeliinek Cohn DeKanv Cynthia Kelly ?lo H. Rver Dr. George M. Semeniuk Richard Denney, Jr., Esq.
Peter 3artcn Hutt
i
Robert M* S us small
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