Guidance for Industry

Guidance for Industry

Nonsterile Semisolid Dosage Forms : Scale-up and Postapproval Changes : Chemistry, Manufacturing, and Controls : in Vitro Release Testing and in Vivo Bioequivalence Documentation

Website or Online Data - 1997
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Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, [1997]
Characteristics: 1 electronic resource (30) p.


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