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Presentation at the FDA’s Public Kickoff Meeting on the Reauthorization of MDUFA

View complete testimony as PDF

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In its presentation at the Food and Drug Administration’s (FDA’s) kickoff public meeting to discuss proposed recommendations for the reauthorization of the Medical Device User Fee Act (MDUFA) for fiscal years 2023 through 2027, Public Citizen expressed its long-standing strong opposition to the FDA’s user fee programs and offered several recommendations for strengthening the agency’s oversight of high-risk, permanently implanted medical devices to better protect patients from unsafe or ineffective products.

See Public Citizen’s other work regarding the medical device review process.