Prescription Drug User Fee Act : Structure and Reauthorization Issues.

Reviews the Prescription Drug User Fee Act (PDUFA) of 1992, which authorizes FDA to impose drug approval application fees on drug manufacturers to fund new drug and biologic product safety review activities. Examines implementation of PDUFA, and discusses reauthorization issues.

Bibliographic Details
Corporate Authors: Library of Congress. Congressional Research Service, ProQuest (Firm)
Format: eBook
Language:English
Published: [Place of publication not identified] : [publisher not identified], 2002.
Series:U.S. Congressional Research.
Subjects:
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Call Number: CRS-2002-DSP-0044
 
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CRS-2002-DSP-0044 Available