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Guidance for industry : postmarketing studies and clinical trials, implementation of section 505(o) of the Federal Food, Drug, and Cosmetic Act.

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 : Center for Biologics Evaluation and Research, [2009]
Subjects:
United States. > Federal Food, Drug, and Cosmetic Act.
Clinical trials > Government policy > United States.
Online Access:https://purl.fdlp.gov/GPO/LPS116720
Description
Item Description:"Draft guidance."
"Drug safety."
"July 2009."
Electronic resource.
Physical Description:1 online resource (13 pages)