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The basic regulatory considerations and prospects for conducting bioavailability/bioequivalence (BA/BE) studies – an overview

Authors Mastan S, Thirunagari BL, Sathe

Published 22 March 2011 Volume 2011:1 Pages 1—25

DOI https://doi.org/10.2147/CER.S15861

Review by Single-blind

Peer reviewer comments 2


Shaik Mastan1, Thirunagari Bhavya Latha2, Sathe Ajay1
1Cytel Statistical Software and Services Pvt Ltd, Pune, Maharashtra, India; 2Business Development, Bioserve Clinical Research Pvt Ltd, Hyderabad, Andhra Pradesh, India

Abstract: Bioavailability (BA) and bioequivalence (BE) studies play a major role in the drug development phase for both new drug products and their generic equivalents, and thus attract considerable attention globally. BE is a strategy to introduce generic equivalents of brand-name drugs (innovator drugs) to lower the cost of medication through proper assessment as directed by the international regulatory authorities. There are several approaches to assess BE and each regulatory authority has its own regulations/guidance for conducting BA/BE studies before approving generic products for marketing in their country. Therefore, a thorough understanding is required of these BA/BE concepts and basic regulatory considerations for conducting BA/BE studies. This article briefly reviews the BA/BE concepts, approaches, designs, and various basic regulatory considerations and prospects for conducting BA/BE studies.

Keywords: bioavailability, bioequivalence, generic drugs, regulatory authority, pharmacokinetics, pharmacodynamics
 

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