[生物等效性评价]。

N. Aoyagi
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引用次数: 1

摘要

根据世卫组织的指导,日本目前正在改进生物等效性试验。本文描述了理想的生物等效性评估,其中使用歧视性受试者,应用置信区间方法,推荐药代动力学数据的对数转换。并讨论了溶出度试验在生物等效性评价中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Assessment of bioequivalence].
Bioequivalence tests in Japan are now under the improvement according to the WHO guidance. This article describes the desirable assessment of bioequivalence where the use of discriminatory subjects, application of confidence interval methods, logarithmic transformation of pharmacokinetic data are recommended. The role of dissolution tests in bioequivalence assessment is also discussed.
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