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Title Guidance for industry [electronic resource] : E2E pharmacovigilance planning.

Imprint

Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : Center for Biologics Evaluation and Research, [2005]

Connect to
Connect to https://permanent.fdlp.gov/websites/www.fda.gov/pdf-archive/ucm073107.pdf

Copies

Location	Call No.	OPAC Message	Status
Axe Federal Documents Online	HE 20.4702:P 49/4	---	Available

Description	18 p. : digital, PDF file
System Details	Mode of access via the FDA web site.
Note	Title from PDF title page (viewed on June 19, 2009).
	"ICH".
	"April 2005".
Bibliography	Includes bibliographical references (p. 17-18).
Subject	Drug development.
	Drugs -- Side effects.
Added Author	Center for Drug Evaluation and Research (U.S.)
	Center for Biologics Evaluation and Research (U.S.)
	International Conference on Harmonisation.
Added Title	E2E pharmacovigilance planning
	Pharmacovigilance planning
Gpo Item No.	0499-T (online)
Sudoc No.	HE 20.4702:P 49/4