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E-REPORT
Title Guidance for industry [electronic resource] : postmarketing studies and clinical trials, implementation of section 505(o) of the Federal Food, Drug, and Cosmetic Act.
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, [2009]

Copies/Volumes

LOCATION CALL # STATUS
 Internet  Electronic Report    AVAILABLE
Description 1 online resource (13 p.)
Note "Draft guidance."
"Drug safety."
"July 2009."
Subject United States. Federal Food, Drug, and Cosmetic Act.
Clinical trials -- Government policy -- United States.
Other Author Center for Drug Evaluation and Research (U.S.)
Center for Biologics Evaluation and Research (U.S.)
Other Title Postmarketing studies and clinical trials, implementation of section 505(o) of the Federal Food, Drug, and Cosmetic Act.