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Title Guidance for industry [electronic resource] : Q7A good manufacturing practice guidance for active pharmaceutical ingredients.

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, [2001]

Copies

Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 20.4702:M 31    ---  Available
Description iv, 52 p. : digital, PDF file
System Details Mode of access via the FDA web site.
Note Title from PDF title page (viewed on June 17, 2009).
"ICH".
"August 2001".
Subject Drug factories -- Quality control.
Pharmaceutical chemistry.
Drugs -- Quality control.
Added Author Center for Drug Evaluation and Research (U.S.)
Center for Biologics Evaluation and Research (U.S.)
International Conference on Harmonisation.
Added Title Q7A good manufacturing practice guidance for active pharmaceutical ingredients
Good manufacturing practice guidance for active pharmaceutical ingredients
Gpo Item No. 0499-T (online)
Sudoc No. HE 20.4702:M 31

 
    
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