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Guideline for the format and content of the nonclinical pharmacology/toxicology section of an application.

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Format:
Book
Government document
Contributor:
Center for Drugs and Biologics (U.S.)
Center for Drug Evaluation and Research (U.S.)
Language:
English
Subjects (All):
Drugs--United States--Testing.
Drugs.
Drugs--Toxicology.
Legislation, Drug.
New drug applications.
Clinical Trials--standards.
Drugs--Testing.
United States.
Medical Subjects:
Legislation, Drug.
New drug applications.
Clinical Trials--standards.
Physical Description:
1 online resource (1 electronic resource (27 pages))
Other Title:
Title from PDF cover: Guidance for industry
Place of Publication:
Rockville, Md. : Center for Drugs and Biologics, Food and Drug Administration, Dept. of Health and Human Services, [1987]
Notes:
"Center for Drug Evaluation and Research"--PDF cover
"February 1987."
Other Format:
Print version: Guideline for the format and content of the nonclinical pharmacology/toxicology section of an application
OCLC:
535261062

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