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 (66 pages, digital, PDF file)

Place of Publication:

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

System Details:

text file

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:

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. FDA Legislation in the 110th Congress

Access Restriction:

Restricted for use by site license.