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.
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Industry Discussions on MDUFA III Reauthorization
- February 17, 2012
- February 16, 2012
- February 14, 2012
- February 10, 2012
- February 8, 2012
- January 31, 2012
- January 5, 2012
- December 13, 2011
- December 6, 2011
- November 29, 2011
- November 18, 2011
- November 10, 2011
- November 3, 2011
- October 31, 2011
- October 26, 2011
- October 21, 2011
- October 6, 2011
- September 29, 2011
- September 13, 2011
- August 31, 2011
- August 24, 2011
- August 9, 2011
- August 2, 2011
- July 26, 2011
- July 15, 2011
- June 27, 2011
- June 17, 2011
- June 1, 2011
- May 4, 2011
- April 13, 2011
- March 30, 2011
- March 7, 2011
- February 23, 2011
- February 9, 2011
- January 26, 2011
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Stakeholder Discussions on MDUFA III Reauthorization
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