Advancing Virtual Bioequivalence for Orally Administered Drug Products: Methodology, Real-World Applications and Future Outlook
Bioequivalence studies are pivotal in generic drug development wherein therapeutic equivalence is provided with an innovator product. However, bioequivalence studies represent significant complexities due to the interplay of multiple factors related to drug, formulation, physiology, and pharmacokine...
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Main Authors: | Sivacharan Kollipara (Author), Frederico Severino Martins (Author), Rebeka Jereb (Author), Dejan Krajcar (Author), Tausif Ahmed (Author) |
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Format: | Book |
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MDPI AG,
2024-07-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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