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GUIDELINES FOR BIOAVAILABILITY & BIOEQUIVALENCE STUDIES Central Drugs Standard Control Organization, Directorate General of Health Services, Ministry of Health & Family Welfare, Government of India,
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Bioavailability amp refers to the measurement of the rate and extent to which an active ingredient is absorbed into the bloodstream to produce an effect.
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Manufacturers of pharmaceutical products are typically required to file bioavailability amp studies as part of the drug approval process.
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