Q&A: From FDA to Industry

Among a subset of US Food and Drug Administration regulators who leave the agency, more than half go to work for pharmaceutical companies, researchers report.

Written byKerry Grens
| 5 min read

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VINAY PRASADMedical reviewers at the US Food and Drug Administration (FDA) decide which drugs make it to market. An analysis of 55 FDA reviewers who approved blood and cancer drugs between 2006 and 2010 found that a substantial number of these individuals went on to work for the industry they were previously regulating.

Vinay Prasad, a hematologist-oncologist at Oregon Health & Science University (OHSU) who coauthored the study with OHSU medical resident Jeffrey Bien, said the results are concerning. Given the possibility of career advancement by moving to industry, Prasad said, “it may make you more likely to want to be agreeable, to get along, to move things through.”

Prasad and Bien’s analysis, published in The BMJ today (September 27), found no impropriety. In an email to The Scientist, an FDA spokesperson said the agency has numerous policies in place to protect against potential conflicts of interest. “Federal laws and FDA ethics rules cover issues like outside employment, avoiding real and apparent conflicts of interest, recusals, disclosure requirements, protecting confidentiality, a ban on gifts from regulated industry, and ...

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  • kerry grens

    Kerry served as The Scientist’s news director until 2021. Before joining The Scientist in 2013, she was a stringer for Reuters Health, the senior health and science reporter at WHYY in Philadelphia, and the health and science reporter at New Hampshire Public Radio. Kerry got her start in journalism as a AAAS Mass Media fellow at KUNC in Colorado. She has a master’s in biological sciences from Stanford University and a biology degree from Loyola University Chicago.

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