FDA's monitoring of postmarketing study commitments

FDA's monitoring of postmarketing study commitments.

Author/creator	United States. Department of Health and Human Services. Office of Inspector General
Format	Electronic and Book
Publication Info	[Washington, D.C.] : Department of Health and Human Services, Office of Inspector General, 2006.
Description	1 online resource (iv, 38 pages) : illustrations
Supplemental Content	https://purl.fdlp.gov/GPO/gpo71089
Subject(s)	United States. Food and Drug Administration--Rules and practice. United States. Food and Drug Administration Modernization Act of 1997. Drugs--United States --Testing. Clinical trials--Government policy --United States.

Portion of title	Food and Drug Administration's monitoring of postmarketing study commitments
Variant title	Running title: FDA's monitoring of postmarketing study commitments
General note	Title from title screen (viewed Aug 9, 2016).
General note	"June 2006."
General note	"OEI-01-04-00390."
General note	GPO Cataloging Record Distribution Program (CRDP).
Bibliography note	Includes bibliographical references (pages 23-28).
Technical rpt number	OEI-01-01-04-00390
GPO item number	0445-B-07 (online)
Govt. docs number	HE 1.75:OEI-01-04-00390

Library	Location	Call Number	Status	Item Actions
Joyner	Electronic Resources	Access Content Online	✔ Available