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第二部分-口服緩控釋制劑的人體生物等效性試驗-資料下載頁

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【正文】 ilability and bioequivalence studies for orally administered drug products: general considerations. , 2022 相關(guān)指導(dǎo)原則(續(xù)) ? European Medicines Agency. Guideline on the investigation of bioequivalence. docs/en_GB/document_library/Scientific_guideline/2010/01/, 2022 ? The European Agency for the Evaluation of Medicinal Products, Human Medicines Evaluation Unit, Committee for Proprietary Medicinal Products. Note for guidance on modified release oral and transdermal dosage forms: Section II (Pharmacokiic and clinical evaluation). , 1999
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