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.
Subjects:	Medical laws and legislation. Medical supplies. User charges. Electronic books.
Online Access:	Connect to the full text of this electronic book

Description
Summary:	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, postmarket surveillance, and other provisions. Includes tables.
Item Description:	Record is based on bibliographic data in ProQuest U.S. Congressional Research Digital Collection (last viewed Dec. 2010). Reuse except for individual research requires license from ProQuest, LLC. CRS Report. Electronic resource.
Physical Description:	1 online resource.