Deregulatory science: Chemical risk analysis in Trump’s EPA

2020 ◽  
pp. 030631272097028
Author(s):  
Becky Mansfield

While critics cast the Trump administration as anti-science, requiring in response vigorous defense of science, analysis of the Trump EPA reveals instead a strategy to develop deregulatory science. In its first 3 years, the Trump EPA introduced and started to implement a variety of new frameworks to remake scientific risk analysis, changing how it assesses exposures, hazards and costs of chemical harms. The article focuses on EPA frameworks associated with the Clean Air Act, Strengthening Transparency in Regulatory Science rule and Toxic Substances Control Act. The new approaches compel the agency to ignore many pathways of exposure and pivotal studies of hazards, include dose-response models that treat pollution as healthful and change how costs and benefits are calculated. Yet it justifies these frameworks in terms of evidence-based decision-making, transparency and the separation of science from politics. According to its political appointees, the Trump EPA stands for scientific integrity, because it is promulgating evidence-based approaches in risk analysis that show regulation to be neither necessary nor appropriate. This is not just rhetoric but represents an effort to engage science to delegitimize environmental regulation. There is continuity between the Trump EPA and past efforts to use science to justify regulatory rollbacks: defending science by demarcating it from non-science is just as much a strategy for deregulation as it is for regulation. A key lesson is that contesting deregulation by declaring it anti-science reflects an impasse, as deregulatory approaches then also seek to take the mantle of science. The alternative to engaging in debate over demarcation is to make explicit the values and interests shaping practices of regulatory science.

Author(s):  
Michael A. Livermore ◽  
Richard L. Revesz

Reviving Rationality: Saving Cost-Benefit Analysis for the Sake of the Environment and Our Health explains how Donald Trump destabilized the decades-long bipartisan consensus that federal agencies must base their decisions on evidence, expertise, and analysis. Administrative agencies are charged by law with protecting values like stable financial markets and clean air. Their decisions often have profound consequences, affecting everything from the safety of workplaces to access to the dream of home ownership. Under the Trump administration, agencies have been hampered in their ability to advance these missions by the conflicting ideological whims of a changing cast of political appointees and overwhelming pressure from well-connected interest groups. Inconvenient evidence has been ignored, experts have been sidelined, and analysis has been used to obscure facts rather than inform the public. The results are grim: incoherent policy, social division, defeats in court, a demoralized federal workforce, and a loss of faith in government’s ability to respond to pressing problems. This experiment in abandoning the norms of good governance has been a disaster. Reviving Rationality explains how and why our government has abandoned rationality in recent years, and why it is so important for future administrations to restore rigorous and even-handed cost-benefit analysis if we are to return to a policymaking approach that effectively tackles the most pressing problems of our era.


1999 ◽  
Vol 01 (03) ◽  
pp. 329-347 ◽  
Author(s):  
REBECCA A. EFROYMSON

The Toxic Substances Control Act (TSCA) is the legislation used by the U.S. Environmental Protection Agency to regulate releases of genetically engineered microorganisms. The rule defining the scope of the notification requirements for releases of microbial products of biotechnology was published in April 1997. The Environmental Protection Agency (EPA) had some latitude regarding the extent to which various categories of microorganisms would be regulated, but the agency was constrained by requirements of TSCA and an interagency agreement about how to regulate products of biotechnology. This paper investigates the extent to which the scope of oversight is based on risk. A risk-based rule is defined as one where the reporting requirements are based on potential for exposure or expected adverse effects. The evolution of the rule is described, and risk-based components are discussed. In conclusion, the scope of oversight of microbial releases is determined to be based on risk to the extent that legislation and institutional constraints permit.


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