TSCA Reform Passes!

After years of hard work and negotiation, the U.S. Senate on Tuesday passed by unanimous consent the bipartisan Frank R. Lautenberg Chemical Safety for the 21st Century Act.  The bill, which now goes to the President for signature, reforms the 40 year-old Toxic Substances Control Act of 1976 and marks the first piece of environmental legislation to pass since 1990.

“We are very grateful to Senators Vitter, Udall and Inhofe and their staffs for their years of hard work and commitment to improving TSCA,” said Kevin Koonce, VI’s VP of Government Affairs.  “The long road to TSCA reform demonstrates that bipartisanship is still possible in Washington DC.  This legislation will finally give greater certainty to American manufacturers while creating new jobs and without stifling innovation.  This should also reassure consumers of the safety of their products and limit the growing patchwork of state regulatory systems for business to try and navigate.”

The bill was a result of more than three years of negotiations and had support from a broad coalition consisting of the chemical industry, product manufacturers, and environmental and public health groups.

The strong bipartisan support displayed in the House and Senate votes is reflective of the hard work from VI members and our partners in associated industries.  We’d like to extend a big THANK YOU to our members for all their hard work to advance TSCA reform.  From meeting with your Representatives at our annual Congressional Fly-in to all the calls and letters you sent Congress, we could not have done this without you.

Bill Highlights:

•    Testing. EPA has new authority to order chemical testing, and is called upon to use tiered testing, screening approaches, test categories, and encourage alternatives to animal testing. EPA will charge fees to evaluate submitted test results.

•    New chemical reviews. EPA must take sensitive subpopulations and intended conditions of use into account. If EPA fails to make a timely determination on a new chemical, the Agency is required to refund the submitter’s filing fee unless the application is found incomplete. Within 90-days of a finding that the safety standard is not met or that testing is required, EPA must publish a decision on whether to issue a significant new use rule. EPA is required to publish a finding that a new chemical meets the law’s safety standard. Commercialization can proceed before publication of EPA’s finding. In addition, the 90-day review period can end early if EPA determines before that date that the substance meets the safety standard.

•    Inventory Reset. Within one year of enactment, EPA will require manufacturers and importers to submit reports within six months on those chemicals listed on the TSCA Chemical Substance Inventory (“Inventory”) that they have manufactured or imported for a non-exempt commercial purpose in the previous 10 years (“active” chemicals). In the interim, TSCA section 8(a) Chemical Data Reporting (CDR)-reported substances will serve as the list of active substances. Processors may be asked to report. EPA must publish a list of these active substances, and publish a rule within one year after that to require substantiation for chemical identities claimed as confidential business information (CBI).  EPA must complete its review of these CBI claims within five years of issuing the active substance list. Inactive substances will remain on the TSCA Inventory, but EPA must be notified before manufacture, import, or processing can commence.

•    Existing chemicals. Last minute changes included doubling the number of chemicals previously proposed for EPA to designate and review in the first three and a half years of the existing chemical review program to 20 high-priority and 20 low-priority substances. Preference is given to highly ranked PBTs and known human carcinogens with high acute and chronic toxicity. Metals will be evaluated within the March 2007 Framework for Metals Risk Assessment. EPA will prioritize and evaluate existing chemicals that may present an unreasonable risk of injury to health or the environment without considering costs or other nonrisk factors. EPA must consider intended conditions of use and include an evaluation of unreasonable risk to potentially exposed or susceptible subpopulations. Industry-requested risk assessments may comprise 25% – 50% of the Agency’s risk evaluation workload.

•    Regulatory controls. To restrict, phase-out, or ban an existing chemical, EPA must consider effects on health and the magnitude of the exposure, the benefits of the chemical substance or mixture for various uses, the reasonably ascertainable economic consequences of the rule, the costs and benefits of the regulatory action, and consider alternatives. However, EPA will no longer be required to select the least burdensome regulatory alternative. Exemptions may be granted for critical or essential uses; disruption of national economy, security or critical infrastructure, and beneficial uses. EPA cannot impose a regulation that duplicates a regulation issued by the Agency or another agency under a different statute.

•    Preemption.  Federal preemption of new and existing state laws applies when EPA finds that a high priority chemical meets the safety standard and when EPA enacts a rule to regulate a chemical that does not meet the safety standard. Any state statute or regulation in existence before April 22, 2016, however, is grandfathered and not subject to preemption. There is no preemption of common law tort claim actions. Between the time EPA publishes the scope of a chemical risk assessment and up to three and a half years while it conducts the assessment, states generally may not enact new laws and regulations regulating the chemical. However, states may submit waiver requests to EPA to regulate a chemical during this period. States also are given up to 18 months after EPA has initiated the prioritization process or published the scope of the risk evaluation, whichever is sooner, to (i) enact a statute or (ii) propose or finalize an administrative action without any preemption while EPA evaluates the chemical. Exemptions from federal preemption include state law adopted pursuant to federal law; reporting, monitoring, or information obligations not otherwise adopted by EPA; and air, water quality, and hazardous waste laws absent a direct conflict with a TSCA regulation.

•    Confidential Business Information (CBI). The legislation establishes processes for protecting CBI and requires written support for claiming protection from disclosure for chemical identity and other information. Only specific manufacturing and processing descriptions, specific volumes, the composition of a mixture, a chemical’s use and function, and sales and marketing information will not require substantiation. There is a ten year time limit on confidentiality claims. Extensions of CBI protection are available for additional ten year terms. There is a presumption that information on uses of chemicals to be banned or phased-out will be fully disclosed to the public.

•    Fees and Penalties. EPA is tasked to update fees for PMN submissions and impose new fees for reviews of test data and risk assessments for existing chemicals. The fees must support 25% of the operating costs of these programs. Small businesses will pay lower fees. The maximum civil penalty for TSCA violations is increased to $37,500, and maximum criminal penalties are increased to $50,000. Individuals may be fined $250,000 as well as up to 15 years imprisonment for willful, imminent endangerment. Organizations may be fined up to $1 million in such case.

•    Articles. EPA may require a premanufacture notification (PMN) for a chemical substance imported as part of an “article” after issuing a rule finding that there is reasonable potential for exposure that justifies notification. EPA can impose prohibitions or restrictions on articles containing chemicals that do not meet the safety standard to the extent necessary to address the identified risks from exposure.

•    Advisory Committee. EPA is instructed to have an advisory committee with representation from government, industry, nongovernmental organizations and academia to advise the Agency on new and existing chemical reviews.

•    Best Science. EPA must use the “best available science” to review chemicals and develop policies and procedures necessary for implementation within two years.

•    Retroactivity. The new law does not modify any rule or order promulgated or issued under TSCA before its effective date.

•    Judicial review. A determination that the safety standard is met is a final Agency action. A determination that the safety standard is not met is not reviewable until EPA issues a final rule regulating the chemical substance.

•    Miscellaneous: Other provisions further regulate export and disposal of mercury compounds, require negotiated reporting for inorganic byproducts, and provide authority to investigate potential cancer clusters. A section in the earlier Senate bill (S. 697) assessing federal resources dedicated to the use of sustainable chemistry was removed. Previously agreed-on provisions providing greater federal seizure authority and changes to export requirements were dropped from the legislation.

© 2016 Keller and Heckman LLP