MDUFMA Performance Reports

MDUFMA was authorized in FY 2003 for five years.  It was re-authorized as MDUFA for five additional years in FY 2008.  Annual performance reports are prepared by FDA’s Office of Policy and Planning in collaboration with the Center for Biologics Evaluation and Research and the Center for Devices and Radiological Health. 

• MDUFMA I (FY 2003 through FY 2007)
• MDUFA II (FY 2008 through FY 2012)

For additional information on these reports, please contact:

Office of Policy and Planning

Food and Drug Administration

10903 New Hampshire Avenue

Building 1, Room 4300

Silver Spring, Maryland 20993-0002

Phone: 301-796-4850

FAX: 301-847-3541