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E-Book/E-Doc

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

Imprint Silver Spring, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research ; Rockville, MD : Center for Biologics Evaluation and Research, [2008]

Copies

Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 20.4802:IM 7    ---  Available
Description 14 p. : digital, PDF file
System Details Mode of access via the FDA CBER web site.
Note Title from PDF title page (viewed on Apr. 23, 2009).
"ICH".
"June 2008".
"Revision 2".
Subject Drug adulteration.
Drugs -- Analysis.
Drug approval -- 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
Gpo Item No. 0499-T-02 (online)
Sudoc No. HE 20.4802:IM 7

 
    
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