Medical Device User Fee and Modernization Act (MDUFMA) Reauthorization.

Provides overview of the FDA review process for medical devices and FDA authority to collect user fees under the Medical Device User Fee and Modernization Act (MDUFMA). Discusses issues relating to MDUFMA reauthorization, including user fees, third party inspections, reprocessed single-use devices,...

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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], 2007.
Series:U.S. Congressional Research.
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Call Number: CRS-2007-DSP-0429
 
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CRS-2007-DSP-0429 Available