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

Bibliographic Details
Corporate Authors: Center for Drug Evaluation and Research (U.S.), Center for Biologics Evaluation and Research (U.S.)
Format: Government Document eBook
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]
Subjects:
Drugs > Labeling > United States.
Biological products > Labeling > United States.
Online Access:https://purl.fdlp.gov/GPO/LPS110438
Description
Item Description:Title from title screen (viewed on Mar. 19, 2009).
"Draft guidance."
"February 2009."
Electronic resource.
Physical Description:11 pages : digital, PDF file.