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Title Guidance for industry [electronic resource] : clinical pharmacology section of labeling for human prescription drug and biological products : content and format.

Imprint Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER) : Center for Biologics Evaluation and Research (CBER), [2009]

Copies

Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 20.4802:P 49/DRAFT    ---  Available
Description 11 p. : digital, PDF file
System Details Mode of access via the FDA web site.
Note Title from title screen (viewed on Mar. 19, 2009).
"Draft guidance."
"February 2009."
Subject Drugs -- Labeling -- United States.
Biological products -- Labeling -- United States.
Added Author Center for Drug Evaluation and Research (U.S.)
Center for Biologics Evaluation and Research (U.S.)
Added Title Clinical pharmacology section of labeling for human prescription drug and biological products
Gpo Item No. 0499-T-02 (online)
Sudoc No. HE 20.4802:P 49/DRAFT

 
    
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