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

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Bibliographic Details
Corporate author / creator:	Library of Congress. Congressional Research Service.
Imprint:	[S.l] : [s.n.], 2008.
Description:	115 p. : digital, PDF file.
Language:	English
Subject:	Food adulteration and inspection. Administrative law. Medical laws and legislation.
Format:	E-Resource U.S. Federal Government Document Book
URL for this record:	http://pi.lib.uchicago.edu/1001/cat/bib/10699210

Hidden Bibliographic Details
Other uniform titles:	ProQuest U.S. Congressional Research Digital Collection.
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.
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.
Other form:	Microfiche version: Library of Congress. Congressional Research Service. FDA Amendments Act of 2007 (P.L. 110-85)

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