Letter to President Biden Opposing the President and CEO of the Biotechnology Innovation Organization as a Candidate for FDA Commissioner October 12, 2021
Letter to the FDA Urging the Agency Not to Grant 510(k) Premarket Clearance for the TriGUARD 3 Cerebral Embolic Protection Device August 17, 2021
Letters, Testimony & Filings Presentation at the FDA’s Stakeholder Meeting on the Reauthorization of MDUFA June 9, 2021
Comments on the FDA’s Proposed Rule Regarding the “Intended Uses” of Marketed Drugs and Medical Devices October 23, 2020
New Public Citizen Report Highlights the FDA’s Reckless Oversight of Implanted Spinal Cord Stimulators for Pain Relief September 1, 2020
Public Citizen Sues FDA for Failing to Respond to Petition to Ban Surgical Device Seprafilm August 27, 2020
Letters, Testimony & Filings Letter to the FDA Criticizing the Agency’s Response to Public Citizen’s Report on Implanted Spinal Cord Stimulators for Pain Relief July 29, 2020
Press Releases Public Citizen Tracker Finds Taxpayers Have Funded $6 Billion in Coronavirus Treatment, Vaccine Development July 16, 2020