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![PDF] The basic regulatory considerations and prospects for conducting bioavailability/bioequivalence (BA/BE) studies – an overview | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/f7e13872d81da37ef0bef45811f8303c900f3753/2-Figure1-1.png "PDF] The basic regulatory considerations and prospects for conducting bioavailability/bioequivalence (BA/BE) studies – an overview | Semantic Scholar")
PDF] The basic regulatory considerations and prospects for conducting bioavailability/bioequivalence (BA/BE) studies – an overview | Semantic Scholar
Current set of major guidelines for bioequivalence studies in Japan... | Download Table
A pragmatic regulatory approach for complex generics through the U.S. FDA 505(j) or 505(b)(2) approval pathways - Klein - 2021 - Annals of the New York Academy of Sciences - Wiley Online Library
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Guideline for Bioequivalence Studies for Different Strengths of Oral Solid Dosage Forms
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PDF) International Guidelines for Bioequivalence of Systemically Available Orally Administered Generic Drug Products: A Survey of Similarities and Differences
