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.
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.
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.
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.
U.S. News (HealthDay 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.
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.