Evaluating the Bioavailability and Bioequivalence of Generic Medications
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Evaluating the Bioavailability and Bioequivalence of Generic Medications
ABSTRACT By law, the U.S. Food and Drug Administration (FDA) is permitted to approve generic versions of brand-name medications without necessarily requiring that research be conducted to prove them
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The Bioavailability and Bioequivalence of Generic Medications http://ow.ly/WNxg
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