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Title Guidance for industry [electronic resource] : Q3A impurities in new drug substances.

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, [2008]

Connect to
Connect to https://permanent.fdlp.gov/LPS113736/LPS113736/www.fda.gov/downloads/RegulatoryInformation/Guidances/ucm127984.pdf

Copies

Location	Call No.	OPAC Message	Status
Axe Federal Documents Online	HE 20.4702:IM 7	---	Available

Description	14 p. : digital, PDF file
System Details	Mode of access via the FDA web site.
Note	Title from PDF title page (viewed on June 15, 2009).
	"ICH".
	"June 2008".
	"Revision 2".
Subject	Drug development -- Government policy -- United States.
	Drug adulteration -- Government policy -- United States.
Added Author	Center for Drug Evaluation and Research (U.S.)
	Center for Biologics Evaluation and Research (U.S.)
	International Conference on Harmonisation.
Added Title	Q3A impurities in new drug substances
	Impurities in new drug substances
Gpo Item No.	0499-T (online)
Sudoc No.	HE 20.4702:IM 7