Public Citizen Calls on Presidential Candidates, Parties to Pledge Not to Use Dangerous, Manipulative Deepfakes
Statement: FDA Must Reject Tanezumab as a Treatment for Osteoarthritis Due to Unacceptable Dangers, Little to No Benefit
Comments regarding the Institute of Medicine’s Report, Medical Devices and the Public’s Health: The FDA 510(k) Clearance Process September 2, 2011
Letter to the FDA Regarding the Apparent Illegal Marketing and Promotion of the LipoTron Medical Device July 18, 2012
Testimony Before the FDA’s Obstetrics and Gynecology Devices Panel of the Medical Devices Advisory Committee Regarding the Essure Female Sterilization Device September 24, 2015