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Title	FDA is issuing more postmarketing requirements, but challenges with oversight persist.
Format	online resource
Internet Access	https://purl.fdlp.gov/GPO/gpo71091
Author	United States. Department of Health and Human Services. Office of Inspector General, author.
Published	[Washington, D.C.] : Department of Health and Human Services, Office of Inspector General, 2016.

SuDoc Number	HE 1.75:OEI-01-14-00390
Item Number	0445-B-07 (online)
Variation of Title	Food and Drug Administration is issuing more postmarketing requirements, but challenges with oversight persist
	Running title: FDA is issuing more postmarketing requirements, but challenges with oversight persist
Description	1 online resource (26 pages) : illustrations
Content Type	text
General Note	Title from title screen (viewed Aug 9, 2016).
	"July 2016."
	"OEI-01-14-00390."
Bibliography	Includes bibliographical references.
Subject	United States. Food and Drug Administration -- Rules and practice.
Subject - LC	Drugs -- United States -- Testing -- Management.
	Clinical trials -- Government policy -- United States.
URL	https://oig.hhs.gov/oei/reports/oei-01-14-00390.pdf

Holdings	All items

OCLC Number	(OCoLC)956500470
CGP Record Link	https://catalog.gpo.gov:443/F/?func=direct&doc_number=000990959&local_base=GPO01PUB
System Number	000990959