CBS News, February 14, 2011. Dr. Diana Zuckerman and Dr. Steven Nissen agree: the FDA needs to enforce more stringent standards for medical devices to ensure that they are safe before entering the market.
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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.
Report Blames Speedy FDA Clearance for Medical Device Recalls
U.S. News, February 14, 2011. Dr. Diana Zuckerman, president of the National Research Center for Women & Families, calls for an overhaul of the FDA’s medical device regulatory process that would prevent unsafe devices from entering the market.
Read More »Most Recalled Medical Devices Received Speedy FDA Review
Los Angeles Times, February 15, 2011. Dr. Diana Zuckerman, president of the National Research Center for Women & Families, cites evidence and says that the FDA’s review process for medical devices is inadequate.
Read More »Study of Recalled Medical Devices Faults Lax FDA Testing Methods
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.
Read More »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.
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