Wednesday, 9 May 2018

My response to the EPA's 'Strengthening Transparency in Regulatory Science'

Incredible things have happened at the US Environmental Protection Agency since Donald Trump was elected. The agency is responsible for creating standards and laws that promote the health of individuals and the environment. During previous administrations it has overseen laws concerned with controlling pollution and regulating carbon emissions. Now, under Administrator Scott Pruitt, the voice of industry and climate scepticism is in the ascendant. 

A new rule that purports to 'Strengthen Transparency in Regulatory Science' has now been proposed - ironically, at a time when the EPA is being accused of a culture of secrecy regarding its own inner workings. Anyone can comment on the rule here: I have done so, but my comment appears to be in moderation, so I am posting it here.


Dear Mr Pruitt

re: Regulatory Science- Docket ID No. EPA-HQ-OA-2018-0259

The proposed rule, ‘Strengthening transparency in regulatory science’ brings together two strands of contemporary scientific activity. On the one hand, there is a trend to make policy more evidence-based and transparent. On the other hand, there has, over the past decade, been growing awareness of problems with how science is being done, leading to research that is not always reproducible (the same results achieved by re-analysis of the data) or replicable (similar results when an experiment is repeated). The proposed rule by the Environmental Protection Agency (EPA) brings these two strands together by proposing that policy should only be based on research that has openly available public data. While this may on the surface sound like a progressive way of integrating these two strands, it rests on an over-simplified view of how science works and has considerable potential for doing harm.

I am writing in a personal capacity, as someone at the forefront of moves to improve reproducibility and replication of science in the UK. I chaired a symposium at the Academy of Medical Sciences on this topic in 2015; this was jointly organised with UK major funders: Wellcome Trust, Medical Research Council and Biotechnology and Biological Science Research Council (https://acmedsci.ac.uk/policy/policy-projects/reproducibility-and-reliability-of-biomedical-research). I am involved in training early career researchers in methods to improve reproducibility, and I am a co-author of Munafò, M. R et al  (2017). A manifesto for reproducible science. Nature Human Behavior, 1(1: 0021). doi:10.1038/s41562-016-0021. I would welcome any move by the US Government that would strengthen research by encouraging adoption of methods to improve science, including making analysis scripts and data open when this is not in conflict with legal/ethical issues. Unfortunately, this proposal will not do that. Instead, it will weaken science by drawing a line in the sand that effectively disregards scientific discoveries prior to the first part of the 21st century when the importance of open data started to be increasingly recognised.

The proposal ignores a key point about how scientific research works: the time scale. Most studies that would be relevant to EPA take years to do, and even longer to filter through to affect policy. Consequences for people and the planet that are relevant to environmental protection are often not immediately obvious: if they were, we would not need research. Recognition, for instance, of the dangers of asbestos, took years because the impacts on health were not immediate. Work demonstrating the connection occurred many years ago and I doubt that the data are anywhere openly available, yet the EPA’s proposed rule would imply that it could be disregarded. Similarly, I doubt there is open data demonstrating the impact of lead in paint or exhaust fumes, or of pesticides such as DDT: does this mean that manufacturers would be free to reintroduce these?

A second point is that scientific advances never depend on a single study: having open scripts and data is one way of improving our ability to check findings, but it is a relatively recent development, and it is certainly not the only way to validate science. The growth of knowledge has always depended on converging evidence from different sources, replications by different scientists and theoretical understanding of mechanisms. Scientific facts become established when the evidence is overwhelming. The EPA proposal would throw out the mass of accumulated scientific evidence from the past, when open practices were not customary – and indeed often not practical before computers for big data were available.

Contemporary scientific research is far from perfect, but the solution is not to ignore it, but to take steps to improve it and to educate policy-makers in how to identify strong science; government needs advisors who have scientific expertise and no conflict of interest, who can integrate existing evidence with policy implications. The ‘Strengthening Transparency’ proposal is short-sighted and dangerous and appears to have been developed by people with little understanding of science. It puts citizens at risk of significant damage – both to health and prosperity -  and it will make the US look scientifically illiterate to the rest of the world.


Yours sincerely


D. V. M. Bishop FMedSci, FBA, FRS


1 comment:

  1. Excellent comment.

    Unfortunately I think the Scott Pruitt's intent is to remove as much valid research from the decision process as is possible. I think he and others would like it to be as completely fact-free as possible.

    As you point out, much of the data for older research will be unavailable. Other research may have used propritary data under a non-release agreement.

    In some cases, confidentiality laws, say in the EU may make it illegal to supply the data, especially to another government.

    The anti-science crowd are cunning. Incredibly short-sighted but cunning.

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