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U.S. Department of Health and Human Services

Medical Devices

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MDUFA Meetings

FDA periodically conducts meetings on the Medical Device User Fee Act (MDUFA) program. The current legislative authority for MDUFA, reauthorized in 2007 by the FDA Amendments Act (FDAAA), will expire in September 2012. FDAAA requires that FDA hold public meetings and conduct discussions with both the regulated industry and stakeholder groups in developing recommendations for the next MDUFA program (FY2013-2017). This page contains information for both the public part of the MDUFA reauthorization process and the discussions FDA holds with industry and stakeholders.