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Guidance on waiver of in vivo bioequivalence requirements

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Guidance on waiver of in vivo bioequivalence requirements

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Recent News

The Authority Begins Quality Testing of Drug Samples for African Countries
November 15, 2024
Ethiopian Food and Drug Authority Inaugurates New Day-care Centre
October 21, 2024
EFDA, AHRI, and USP/PQM Plus Collaborate with Local Pharmaceutical Manufacturers to Implement National Bioequivalence Roadmap
October 21, 2024

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