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Guidance topical dermatologic corticosteroids, in vivo bioequivalence

Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, [1995] 1995

Guideline for submitting documentation for the manufacture of and controls for drug products

Rockville, Md. : Center for Drugs and Biologics, Food amd [sic] Drug Administration, U.S. Dept. of Health and Human Services, [1987] 1987

Guideline for the format and content of the microbiology section of an application

Rockville, MD : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, [1990] 1990

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

Rockville, Md. : Center for Drugs and Biologics, Food and Drug Administration, Dept. of Health and Human Services, [1987] 1987

A review of FDA's implementation of the Drug Export Amendments of 1986

Rockville, MD : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Biologics Evaluation and Research, [1990] 1990

Guidance for industry and clinical investigators the use of clinical holds following clinical invest

Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research : Center for Drug Evaluation and Research, [2004] 2004