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机构 日期 题名 作者
臺大學術典藏 2018-09-10T06:57:52Z In vitro dissolution profile comparison- Statistics and analysis of the similarity factor, f2 Shah, V.P.; Tsong, Y.; Sathe, P.; Liu, J.-P.; Shah, V.P.; Tsong, Y.; Sathe, P.; Liu, J.-P.; JEN-PEI LIU
臺大學術典藏 2018-09-10T06:57:52Z Design and Analysis of Bioavailability and Bioequivalence, third edition JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU
臺大學術典藏 2018-09-10T06:57:52Z Design and Analysis of Bioavailability and Bioequivalence, third edition JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU
臺大學術典藏 2018-09-10T06:57:52Z Design and Analysis of Bioavailability and Bioequivalence, third edition JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU
臺大學術典藏 2018-09-10T06:57:52Z Design and Analysis of Clinical Trials: Concepts and Methodologies Jen-Pei Liu; JEN-PEI LIU; JEN-PEI LIU
臺大學術典藏 2018-09-10T06:57:52Z Design and Analysis of Clinical Trials: Concepts and Methodologies Jen-Pei Liu; JEN-PEI LIU; JEN-PEI LIU
臺大學術典藏 2018-09-10T06:57:52Z Design and Analysis of Clinical Trials: Concepts and Methodologies Jen-Pei Liu; JEN-PEI LIU; JEN-PEI LIU
臺大學術典藏 2018-09-10T06:57:51Z On statistical evaluation of the linearity in assay validation Hsieh, E.;Liu, J.-P.; Hsieh, E.; Liu, J.-P.; JEN-PEI LIU
臺大學術典藏 2018-09-10T06:57:51Z Commentary on "accounting for the interim safety monitoring of an adverse event upon termination of a clinical trial" Liu, J.-P.; Liu, J.-P.; JEN-PEI LIU
臺大學術典藏 2018-09-10T06:57:51Z A two-stage design for drug screening trials based on continuous endpoints Tsou, H.-H. and Hsiao, C.-F. and Chow, S.-C. and Liu, J.-P.; JEN-PEI LIU

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