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.
NPR. February 14, 2011. Dr. Diana Zuckerman, president of the National Research Center for Women & Families, expresses her surprise at her study’s findings, that the vast majority of medical devices later recalled as high-risk or potentially deadly were never tested on humans or animals.
2011 CPTF President Dr. Diana Zuckerman advises women with breast implants not to get too worried about the connection between breast implants and a rare form of lymphoma, but to see their doctors if they have any concern in this ABC news story.