EDF Health

Selected tag(s): Lautenberg Act

Is there no limit to industry’s overreach and hubris when it comes to new chemicals under TSCA?

By / Published: December 12, 2017

Richard Denison, Ph.D., is a Lead Senior Scientist.

We’ve already blogged about how changes the agency is making to its reviews of new chemicals under the Toxic Substances Control Act (TSCA) are illegal as well as bad policy.  But an industry letter and attachment added last week to EPA’s new chemicals docket shows the chemical industry isn’t done yet in seeking to eviscerate the program.

The letter and position statement were submitted to Jeffery Morris, Director of EPA’s Office of Pollution Prevention and Toxics (OPPT) by something called the TSCA New Chemicals Coalition (NCC).

They raise a multitude of red flags.

The NCC is a creation of the industry law firm Bergeson & Campbell (B&C). The letter to Morris describes NCC as “a group of representatives from over 20 companies that have come together to identify new chemical notification issues under the amended Toxic Substances Control Act (TSCA) and to work collaboratively with you and your team to address them.”

First red flag:  Nowhere are the 20+ companies identified, not in the letter or associated position statement, nor on B&C’s web pages for NCC.  Such secrecy always sets off an alarm when it comes to the chemical industry’s history of forming misleading front groups and coalitions.  Why don’t the companies want their identities known?

Second red flag:  The NCC letter and position statement claim that “OSHA has in place an extensive regulatory scheme, as well as enforcement mechanisms, governing chemical exposure in the workplace” and refers to the “robust nature of the existing OSHA regulatory program” and its “overarching and comprehensive requirements” that apply in the workplace.  Now, anyone outside of industry readily acknowledges that OSHA’s ability to adequately address workplace exposures has been decimated over time – through sustained industry efforts on many fronts, including mounting legal challenges to OSHA’s authority and successfully pressing for reduction after reduction in its budget and staffing.  Those attacks continue today, and if anything have accelerated under the Trump Administration.

Why then, you may wonder, is NCC writing to the director of EPA’s TSCA office to tout OSHA’s sweeping authority over workplace chemical exposures?  By now you may be getting a sense of where this is headed … .   Read More »

Posted in Health policy, Industry influence, Regulation, TSCA reform / Also tagged , | Comments are closed

EDF comments at EPA’s public meeting on identifying chemicals for prioritization stress legal requirements and urge adoption of sound and fair policies

By / Published: December 11, 2017

Richard Denison, Ph.D., is a Lead Senior Scientist.

EPA held a public meeting today on “Approaches to Identifying Potential Candidate Chemicals for Prioritization” under last year’s reforms made to the Toxic Substances Control Act (TSCA) by the Lautenberg Act.

EPA provided brief opportunities for stakeholders to provide comments.  Four of us from EDF gave oral comments at the meeting.  Below we provide links to those comments in written form and briefly describe them (in the order in which they were presented).

EDF Senior Attorney Robert Stockman’s comments argue that, under the law, EPA:

  • must use its broad information-gathering authorities under section 4, 8 and 11 of TSCA to collect all “reasonably available information” to inform the prioritization process;
  • should exercise those authorities in the processes leading up to and including prioritization; and
  • should start immediately to develop additional information on chemicals in its Work Plan.

EDF Project Manager Lindsay McCormick’s comments:

  • stress the need to use its information-gathering authorities to develop experimental data early in the prioritization process;
  • caution against over-reliance on voluntary information submissions;
  • urge EPA to avoid implanting a bias toward information-rich chemicals; and
  • remind EPA of its obligations to make full health and safety studies and underlying data publicly available.

My comments:

  • stress that the law sets a higher bar for low-priority than for high-priority designations;
  • urge EPA to identify only small numbers of low-priority candidates at a time;
  • caution EPA not to identify categories of chemicals as candidates for low-priority designations; and
  • argue EPA should consider ensuring a minimum set of hazard data is available for candidates.

EDF Senior Scientist Dr. Jennifer McPartland’s comments point to serious limitations and critical caveats relating to some of EPA’s proposed approaches for identifying candidates, including:

  • Canadian Categorization and Chemicals Management Plan;
  • Safer Choice Ingredient List; and
  • Functional category approaches.
Posted in Health policy, Health science, TSCA reform / Also tagged , | Comments are closed

CBS News covers a chemical’s tragic impact; points to urgent need to ban high-risk uses of methylene chloride

By Lindsay McCormick / Published: December 7, 2017

Lindsay McCormick is a Project Manager.  

This morning, CBS News focused on the tragic story of Kevin Hartley—a young man who died at the age of 21 while working with a product that contains methylene chloride. Kevin’s story, powerfully relayed by his mother Wendy, illustrates the need to ban high-risk uses of this chemical.

As we have previously noted, in January, the Environmental Protection Agency (EPA) proposed to ban methylene chloride in paint and coating removal products. The agency based its proposal on an extensive assessment of the scientific literature, which demonstrated not only lethal risks from acute exposures to methylene chloride but also a host of other acute and chronic health impacts, like harm to the central nervous system, liver toxicity, and cancer.

Products containing this chemical can be readily found in most hardware stores in America and more tragedies are all but certain, if EPA does not promptly finalize its proposed ban.

The ongoing debates in Washington over the implementation of a new chemical safety law passed just last year are often dense and dry. In sharing her son Kevin’s story, Wendy Hartley reminds us that how these policies are applied has a very real human impact. That is why EDF continues to demand EPA better protect American families from toxic chemicals like the one highlighted by CBS News today.

Please watch the story: https://www.cbsnews.com/news/dangers-of-common-paint-stripper-chemical-methylene-chloride/

Posted in Public health, TSCA reform / Also tagged , , | Read 1 Response

EDF comments at EPA’s public meeting on new chemical reviews question the credibility and legality of recent changes

By / Published: December 6, 2017

Richard Denison, Ph.D., is a Lead Senior Scientist.

EPA held a public meeting today to present information on major changes it is making to its review of new chemicals under last year’s reforms made to the Toxic Substances Control Act (TSCA) by the Lautenberg Act.

EPA provided brief opportunities for stakeholders to provide comments.  Two of us from EDF – I, and my colleague Robert Stockman, Senior Attorney – gave oral comments at the meeting.  We are providing those comments here in written form.[pullquote]Through these actions, many clearly contrary to the law, EPA is returning the new chemicals program to its dark ages under the old TSCA, making it again into a black box within which EPA acts as if its only stakeholder is the chemical industry.[/pullquote]

My comments are available here.

Robert Stockman’s comments are available here.

As the comments make clear, EDF believes the changes EPA is making and discussed today are both contrary to the requirements of the new TSCA and represent a retreat from the credible, transparent and accountable new chemicals program Congress sought to establish under the new law.

As I noted in my comments:  “Through these actions, many clearly contrary to the law, EPA is returning the new chemicals program to its dark ages under the old TSCA, making it again into a black box within which EPA acts as if its only stakeholder is the chemical industry.”

Posted in Health policy, Industry influence, Regulation, TSCA reform / Also tagged , , | Comments are closed

Too little, too late: Why SNURs alone are not a sufficient alternative to consent orders for new chemicals

By / Published: November 30, 2017

Richard Denison, Ph.D., is a Lead Senior Scientist.

The Environmental Protection Agency (EPA) is in the process of making some major changes to its policies and practices governing new chemical reviews.  This post discusses one of the most troubling ones.  [pullquote]The SNUR-only approach EPA is now deploying differs dramatically from and provides far less risk protection than would result from it simply doing what the law requires:  using orders, with SNURs as backup.[/pullquote]

As I have previously described, last year’s Lautenberg Act made extensive changes to section 5 of the Toxic Substances Control Act (TSCA), which governs the review of new chemicals prior to their manufacture and use.  Among these changes is a requirement that EPA must evaluate potential risks, and mitigate potential unreasonable risks, of a new chemical under its “conditions of use,” which the new law defines to include “reasonably foreseen” circumstances of production, processing, distribution, use or disposal, as well as those intended by the company submitting notice of the new chemical to EPA.  If EPA identifies potential risk or significant exposure or lacks sufficient information on a new chemical, it must issue an order prohibiting or limiting the conditions of use of the chemical in order to mitigate any unreasonable risk.

After passage of the Lautenberg Act until recently, and in keeping with the new law, if EPA’s review identified risk concerns relating to conditions of use beyond those strictly identified by a company submitting a new chemical notice to EPA, the agency made a “may present an unreasonable risk” finding and pursued development of a consent order with the company sufficient to ameliorate those concerns.  (While EPA has authority to issue unilateral orders, it typically negotiates with the company to arrive at a consent order that both parties sign.)

Now EPA is indicating it will instead make a “not likely to present an unreasonable risk” finding for the intended conditions of use, and says it can address any concerns over reasonably foreseen uses without issuing an order by developing only a significant new use rule (SNUR).  This “SNUR-only approach” is inconsistent with the law, a matter I won’t discuss further here.  However, it also raises a host of policy concerns, some of which I lay out in this post.

The SNUR-only approach EPA is now deploying differs dramatically from and provides far less risk protection than would result from it simply doing what the law requires:  using orders, with SNURs as backup.

There are ample reasons why Congress called on EPA to use orders to address concerns and then use SNURs as backup:  Orders (including consent orders) and SNURs are not created equal.  This post discusses 12 key differences, with respect to:

(Spoiler alert:  Deep dive ahead. Let me apologize to and warn readers in advance that this post gets rather into the weeds, as the issues are complicated and the details are important.)   Read More »

Posted in Health policy, Regulation, TSCA reform / Also tagged , , | Comments are closed

More questions for EPA on identifying chemicals for prioritization under TSCA

By Lindsay McCormick / Published: November 29, 2017

Lindsay McCormick is a Project Manager.  

When EPA finalized its framework prioritization rule under TSCA last June, the agency deleted its proposed approach to identifying potential candidate chemicals for prioritization.  EDF had supported EPA’s initial proposed rule, and EPA’s decision to delay this process to allow for additional stakeholder engagement tracks closely with the comments chemical industry groups submitted on that proposed rule.

EPA is now holding a public meeting on December 11th to discuss its proposed approaches and get input from stakeholders.  As with the upcoming meeting on new chemical reviews, EPA is accepting questions ahead of the meeting.

In response, EDF submitted a number of questions to the agency on Monday, relating to our concerns in the following areas:

  • EPA’s stated intention to significantly exceed its statutory minimum of designating 20 low-priority chemicals within the law’s specified timeframe.
  • EPA’s passive approach to utilizing its new authorities to fill data gaps on chemicals before they enter the prioritization and risk evaluation processes.
  • The need to ensure transparency with respect to health and safety studies and underlying data used by EPA to identify candidate chemicals for prioritization.
  • Specific concerns regarding EPA’s proposed approaches, including to utilize Canada’s Chemicals Management Plan as a model and to use EPA’s Safer Chemicals Ingredient List (SCIL) as a basis for identifying low-priority chemicals.

Read our full list of questions here for more details.

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