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version dated 13 November 2008.8.Bioavailability and Bioequivalence Studies for Orally Administered DrugProducts-General Considerations; Guidance for Industry; US Department of Healthand Human Services, Food and Drug Administration, Center for Drug

Evaluationand Research,Washington, D.C., March 2003.声明：本文由药事纵横编辑Herman翻译，转载务必获得药事纵横许可，并注明来源和作者（原作者和翻译作者），否则一律认定为侵权。作者微信号：Hermans807，欢迎探讨与交流。