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

Format:

Book

Government document

Author/Creator:

Library of Congress. Congressional Research Service.

Language:

English

Subjects (All):

Medical laws and legislation.

Medical supplies.

User charges.

Physical Description:

1 online resource (26 pages, digital, PDF file)

Place of Publication:

[Place of publication not identified] : [publisher not identified], 2007.

System Details:

text file

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.

Notes:

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.

Other Format:

Microfiche version: Library of Congress. Congressional Research Service. Medical Device User Fee and Modernization Act (MDUFMA) Reauthorization

Access Restriction:

Restricted for use by site license.