The Evaluation of Average Bioequivalence Using a Modified Anderson-Hauck’s Test

碩士 === 國立成功大學 === 統計學系碩博士班 === 93 === Only after the patent of a brand-name innovative drug product is expired, its generic copies are allowed to market. However, regulatory approval requires evidence of bioequivalence based on the pharmacokinetic responses derived from the time-plasma concentration...

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Bibliographic Details
Main Authors: Wei-Hang Chen, 陳韋翰
Other Authors: Mi-Chia Ma
Format: Others
Language:en_US
Published: 2005
Online Access:http://ndltd.ncl.edu.tw/handle/19755705224003622903