Guidance for industry : waiver of in vivo bioavailability studies for immediate-release soild oral dosage forms based on a biopharmaceutics classification system.

Bibliographic Details
Corporate Author:	Center for Drug Evaluation and Research (U.S.)
Format:	Government Document eBook
Language:	English
Published:	Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, [2000]
Subjects:	Drugs > United States > Dosage forms > Bioavailability. Drugs > United States > Therapeutic equivalency. Biopharmaceutics.
Online Access:	https://purl.fdlp.gov/GPO/LPS120576

Available Online