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Subjects (1-6 of 6)
Drugs United States Therapeutic Equivalency
1
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
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Axe Federal Documents Online
HE 1.2:G 28/2
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Available
2
ElectronicResource GovDoc
Guidance topical dermatologic corticosteroids, in vivo bioequivalence
Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, [1995] 1995
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Axe Federal Documents Online
HE 20.4702:C 81
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3
ElectronicResource GovDoc
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
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Axe Federal Documents Online
HE 20.4702:B 52/5
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4
ElectronicResource GovDoc
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
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Axe Federal Documents Online
HE 20.4702:C 62
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5
ElectronicResource GovDoc
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
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Axe Federal Documents Online
HE 20.4702:B 52/6
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Available
6
ElectronicResource GovDoc
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
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Axe Federal Documents Online
HE 20.4702:B 52/7
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