The Washington Post, February 14, 2011. Dr. Diana Zuckerman, president of the National Research Center for Women & Families, publishes an article that reveals critical flaws in the FDA’s current review system for medical devices.
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As a respected nonprofit health research center, our views are often quoted in the media, including newspapers, magazines, TV, radio, and websites. We also write articles and blogs for a number of different and highly respected newspapers, magazines, and popular websites, and we are published in prestigious medical journals and health policy publications. We frequently express our policy views in letters to government officials and public comments to federal agencies and we sometimes release statements or press releases on newsworthy issues.
Please e-mail info@center4research.org or call 202-223-4000 with your inquiries. We can assist you with scheduling interviews with the NCHR President, Dr. Diana Zuckerman, and other experts on our staff.
Recalled Medical Devices Undergo Little Testing, Study Finds
Milwaukee Journal Sentinel, February 14, 2011. Dr. Diana Zuckerman and Paul Brown of the National Research Center for Women & Families publish a study that finds that the vast majority of recalled medical devices were approved by the FDA using lax standards.
Read More »Recalled Devices Mostly Untested, New Study Says
New York Times, February 14, 2011. Dr. Diana Zuckerman and Paul Brown of the National Research Center for Women & Families publish study that finds that a vast majority of recalled medical devices that are intended to save lives were not tested on humans or animals.
Read More »Medical Device Recalls Reveal Cracks in Regulatory Procedures, Researchers Say
ABC News, February 14, 2011. The story of one of the millions of patients whose implanted medical devices were recalled after being approved by lax FDA standards, as revealed in a study by Dr. Diana Zuckerman, president of the National Research Center for Women & Families.
Read More »Device Review Process Faulted
Wall Street Journal, February 15, 2011. A study published by lead author Dr. Diana Zuckerman, president of the National Research Center for Women & Families, finds that reform of the FDA’s regulatory process for medical devices is needed in order to ensure safety.
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