The bioequivalence study design recommendations for immediate-release solid oral dosage forms in the international pharmaceutical regulators programme participating regulators and organisations: differences and commonalities
Bioequivalence (BE) studies are considered the standard for demonstrating that the performance of a generic drug product in the human body is sufficiently similar to that of its comparator product. The objective of this article is to describe the recommendations from participating Bioequivalence Wor...
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Frontiers Media S.A.,
2024-03-01T00:00:00Z.
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Internet
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A1234.567 |
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Kopya Bilgisi 1 | Kütüphanede |