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Expanding the use of generic drugs.

[Washington, D.C.] : Office of the Assistant Secretary for Planning and Evaluation, Office of Science and Data Policy, U.S. Department of Health and Human Services, 2010. 2010

Guidance topical dermatologic corticosteroids, in vivo bioequivalence

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

Guidance for industry bioavailability and bioequivalence studies for nasal aerosols and nasal sprays

Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, [2003] 2003

Guidance for industry clozapine tables, in vivo bioequivalence and in vitro dissolution testing.

Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, [2005] 2005

Guidance for industry statistical approaches to establishing bioequivalence.

Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, [2001] 2001

Guidance for industry waiver of in vivo bioavailability studies for immediate-release soild oral dos

Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, [2000] 2000