FDA Legislation in the 110th Congress A Side-by-Side Comparison of S. 1082 and H.R. 2900

Format:

Book

Government document

Author/Creator:

Library of Congress. Congressional Research Service

Language:

English

Subjects (All):

Medical laws and legislation.

Medical supplies.

Product safety.

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 side-by-side comparison of provisions of S. 1082, the Food and Drug Administration Revitalization Act of 2007, and H.R. 2900, the Food and Drug Administration Amendments Act of 2007, both to reauthorize existing FDA programs and expand FDA authority to ensure safety of prescription drugs, medical devices, and biologics

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 FDA Legislation in the 110th Congress

Publisher Number:

CRS-2007-DSP-0671

Access Restriction:

Restricted for use by site license