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Guidance for industry clinical pharmacology section of labeling for human prescription drug and biological products : content and format.

Other Authors: Center for Drug Evaluation and Research (U.S.), Center for Biologics Evaluation and Research (U.S.)
Format: Electronic
Language: English
Published: 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]
Physical Description: 11 pages : digital, PDF file.
Subjects:
Drugs -- Labeling -- United States.
Biological products -- Labeling -- United States.
Online Access: https://purl.fdlp.gov/GPO/LPS110438
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