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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.

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Format:
Book
Government document
Contributor:
Center for Drug Evaluation and Research (U.S.)
Center for Biologics Evaluation and Research (U.S.)
Language:
English
Subjects (All):
United States. Federal Food, Drug, and Cosmetic Act.
United States.
Federal Food, Drug, and Cosmetic Act (United States).
Clinical trials--Government policy--United States.
Clinical trials.
Clinical trials--Government policy.
Physical Description:
1 online resource (13 pages)
Other Title:
Postmarketing studies and clinical trials, implementation of section 505(o) of the Federal Food, Drug, and Cosmetic Act
Place of Publication:
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]
Notes:
"Draft guidance."
"Drug safety."
"July 2009."
OCLC:
466868919

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