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Survey: Despite Progress, FDA Scientists Feel Political and Industry Pressure

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UCS released a survey of 997 FDA scientists this morning which found that while FDA leaders are working hard to boost scientific integrity at the agency, persistent interference by special interests continues to hinder scientists’ work.  The FDA responded quickly and reasonably, stressing its successes while acknowledging that improvements can and should be made. National Public Radio science reporter Nell Greenfieldboyce was first out of the gate with a quick summary of the findings and FDA’s response.

An FDA microbiologist tests seafood for microorganisms.

An FDA microbiologist tests seafood for microorganisms.

The survey can be compared to another survey of FDA scientists completed by UCS in 2006. In the survey released today, the scientists told us the agency is moving in the right direction, and they feel more supported by supervisors and FDA leadership. FDA scientists express concern on several fronts, including their right to publish research and communicate with the public, the degree of corporate and political influence on regulatory decisions, and the overall transparency and accountability of the agency’s decision making.

In short, the survey tells us that the problems FDA faces are deeply systemic, and that strong leadership isn’t enough to eliminate political interference in decision-making at the agency.

Next Steps

First, I’m encouraged by the fact that the FDA last month released a scientific integrity policy. But the agency should now formally seek public comment on that policy to help strengthen it. As the president’s science advisor has said, scientific integrity policies tend to improve considerably as a result of public input.

Second, the FDA’s demonstrated progress should serve as a warning to Congress to keep its hands off reforms that have increased the FDA’s independence. In 2007, in light of numerous product recalls and congressional scrutiny of FDA scientists whose work was suppressed and censored, Congress approved the Food and Drug Administration Amendments Act. That law required that the FDA be more transparent in its drug approval process, and directed the agency to reduce the number of experts on its advisory panels who have financial stakes in panel recommendations.

This year, Congress is again considering major FDA legislation, part of its must-pass reauthorization of the Prescription Drug User Fee Act and the Medical Device User Fee Act. The fragile progress that the FDA has made, as evidenced by this survey, would be harmed by legislative proposals now pending before lawmakers, which would relax conflict of interest standards and make science at the agency significantly more vulnerable to special-interest pressures. One legislative proposal would actually change the FDA’s mission to include job creation, diluting its core obligation to protect American families from unsafe drugs, food, and medical devices.

The FDA is big and complex—according to the agency, it is responsible for the safety of items accounting for 25 cents of every dollar spent by consumers.  It is important for the agency to continue the progress it has made in restoring scientific integrity to federal policymaking. It is equally important for Congress to build upon the reforms that are already in place.

Posted in: Scientific Integrity Tags: , , , , , , ,

About the author: Francesca Grifo is an expert on political interference in science and practices to ensure transparency and integrity at the intersection of science and policy. In addition, Dr. Grifo has more than 30 years of experience in environmental issues including biodiversity conservation, environmental education and global change and human health. She holds a Ph.D. in botany. Subscribe to Francesca's posts

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2 Responses

  1. The USC survey confirms my experience with the FDA and the medical device industry. I have been advocating for federal public policy legislative changes for safer implanted medical devices since 2008. In 2010 I was invited to a workshop for Patient Representatives. I learned that even if OSHI (office of special health issues) selected me for the Orthopaedic & Rehabilitation Devices Advisory Panel, I would not be allowed to vote as a full stakeholder and 96% were processed through 510(k). There was no mechanism for patients to contact the person holding that Patient Representative position, nor indication of how that Patient Representative actually represented real life patients. Rather than investigating the MedWatch Adverse Event that our family patient-reported, FDA evaded the FOI request by stating that the report could not be located. Vulnerable patients are exploited by a very entitled for-profit industry. FDA scientists are a very thin (but appreciated) armor for this confrontation.

    • Howard Sadwin says:

      I have offered, as a lay person, the use of my common sense and business logic. I can be objective,even though I have no quality of life as I once had, thankyou MOM hip. The FDA keeps additing more+more patches to a roof that has been leaking for fourty years; time fopr a new one. All these new and wonderful action they are planning on implementing, due to the current rise in pressure they are receiving for approving medical devices, that are hurting people badly, the FDA hasn’t protecting the health & well being of us human beings. Not only is there very little apparent control of this organization,how is FDA planning on implementing fines,with more wrist slapping warning letters? Does the FDA work for the people or do they really work for the medical device world.
      Howard Sadwin