Fixing a toxics “quagmire” at EPA: the role of risk assessment in chemical policy reform
Posted by
Molly Rauch, MPH
on
September 16, 2010
If you’ve heard about proposed reforms of the Toxic
Substances Control Act (TSCA), you may have also heard about a set of
recommendations of the National Academy of Sciences (NAS), the nation’s top
scientific experts, for assessing chemical safety. Health professionals,
environmental groups, and scientific researchers, as well as local community
groups around the country, affirm that incorporating the NAS recommendations
into TSCA reform is an important step in crafting a chemicals management system
that effectively protects human health. In today’s post, I try to explain why
we’ve all been talking about this wonky NAS report.
The Toxic Substances Control Act (TSCA) regulates the vast
majority of industrial chemicals manufactured and used in the US. The law,
enacted in 1976, has a marked pro-industry approach, and has proven toothless
in allowing the EPA to regulate even those toxicants widely known to harm
health, such as asbestos. (Yup, it’s true. The
known carcinogen is still legal for a variety of uses in the US.) PSR
has long argued that the
chemicals management system is broken and needs a health-protective
overhaul.
A new bill introduced in Congress over the summer -- the Toxic Chemicals Safety
Act (H.R. 5820) – aims to do just that, and, together with the Safer Chemicals Healthy Families
coalition, PSR has been optimistic that this legislation could lead to greater
health protections and, ultimately, better health for American citizens.
There are several exciting
policy approaches outlined in the new bill. One is a requirement that the
chemical industry demonstrate that chemicals are safe, rather than the EPA
having to prove they are unsafe. Another provision makes it harder for industry
to keep chemical information secret. Yet another is the requirement that the
Environmental Protection Agency relies on the National
Academy of Sciences’ recommendations to incorporate the best and latest
science when determining the safety of chemicals.
So, what exactly does that last item mean?
At a Congressional briefing yesterday, Thomas Burke, PhD,
the Chair of the National Academy of Sciences panel that crafted the
aforementioned recommendations, addressed the question of how risk assessment
can be more health-protective. The NAS panel he chaired created a step-wise
process to use existing science for decision-making, even in the face of
scientific uncertainty.
Dr. Burke characterized EPA’s risk assessment process as a
“quagmire.” Among many problems with the process, Dr. Burke explained that the
agency’s risk assessments have not generally accounted for variability in human
susceptibility to toxic chemicals. Moreover, current risk assessments are not
adequately capturing multiple exposures to chemicals, complex mixtures of
chemicals, and the fact that some populations are disproportionately exposed to
chemicals. EPA needs a cumulative risk assessment strategy that takes all these
things into account, he said.
The chemical manufacturing industry, mainly in the form of the American
Chemistry Council, has vehemently opposed the health-protective policies
laid out in the Toxic Chemicals Safety Act. Dr. Burke expressed frustration
with the way such opposition cites science and scientific uncertainty in
particular as the best justification for avoiding stronger regulation. “Science
has become a surrogate battleground for the debate on regulation,” he said,
affirming that effective regulation can be implemented even in the face of
uncertainty. That’s why we have a risk assessment process, and that’s why that
process needs to be as current and rigorous as possible.
Now we need to make sure that the system regulating the
manufacture and use of chemicals in our country reflects this need. When the
NAS recommendations are incorporated into our chemicals management system,
Americans will be healthier.
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