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

Contained In:

ProQuest U.S. Congressional Research Digital Collection

Place of Publication:

[Place of publication not identified] [publisher not identified] 2007

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, other provisions, and FDA agreement recommendations. Includes tables

Notes:

CRS Report

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

Vendor supplied data

Other Format:

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

Publisher Number:

CRS-2007-DSP-0609

Access Restriction:

Restricted for use by site license