FDA Amendments Act of 2007 (P.L. 110-85).

Examines and summarizes provisions of P.L. 110-85, the Food and Drug Administration Amendments Act (FDAAA) of 2007, which reauthorizes four expiring FDA programs; and expands FDA authority to regulate the safety of prescription drugs and biologics, medical devices, and foods. Provides side-by-side-c...

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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], 2008.
Series:	U.S. Congressional Research.
Subjects:	Food adulteration and inspection. Administrative law. Medical laws and legislation. Electronic books.
Online Access:	Connect to the full text of this electronic book

Description
Summary:	Examines and summarizes provisions of P.L. 110-85, the Food and Drug Administration Amendments Act (FDAAA) of 2007, which reauthorizes four expiring FDA programs; and expands FDA authority to regulate the safety of prescription drugs and biologics, medical devices, and foods. Provides side-by-side-comparison of provisions of FDAAA and previous law.
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.