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...
Main Authors: | , |
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Other Authors: | |
Format: | Others |
Language: | en_US |
Published: |
2005
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Online Access: | http://ndltd.ncl.edu.tw/handle/19755705224003622903 |