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Showing items 11-20 of 43 (5 Page(s) Totally) << < 1 2 3 4 5 > >> View [10|25|50] records per page
| 臺大學術典藏 |
2018-09-10T06:24:53Z |
A two one-sided tests procedure for assessment of individual bioequivalence
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Liu, J.;Chow, S.-C.; Liu, J.; Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:24:52Z |
Statistical evaluation of similarity factor f2 as a criterion for assessment of similarity between dissolution profiles
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Liu, J.-P.;Ma, M.C.;Chow, S.-C.; Liu, J.-P.; Ma, M.C.; Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:18Z |
The impact of outlying subjects on decision of bioequivalence
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Ki, F.Y.C.;Liu, J.-P.;Wang, W.;Chow, S.-C.; Ki, F.Y.C.; Liu, J.-P.; Wang, W.; Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:18Z |
Replicated crossover designs in bioavailability and bioequivalence trials
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Liu, J.-P.;Chow, S.-C.; Liu, J.-P.; Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:18Z |
Current issues in bioequivalence trials
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Chow, S.-C.;Liu, J.-P.; Chow, S.-C.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:49:26Z |
Recent statistical developments in bioequivalence trials - A review of the FDA guidance
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Chow, S.-C.;Liu, J.-P.; Chow, S.-C.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:09:26Z |
Sample size determination for the two one-sided tests procedure in bioequivalence
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Liu, J.-p.;Chow, S.-C.; Liu, J.-p.; Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:09:26Z |
Bridging studies in clinical development
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Liu, J.-P.; Chow, S.-C.; JEN-PEI LIU; Liu, J.-P.;Chow, S.-C. |
| 臺大學術典藏 |
2018-09-10T04:09:26Z |
On the assessment of variability in bioavailability/bioequivalence studies
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Liu, J.-P.;Chow, S.-C.; Liu, J.-P.; Chow, S.-C.; JEN-PEI LIU |
| 國立臺灣大學 |
2009-12 |
Design and Analysis of Clinical Trials, 2nd Edition, Abbreviate Chinese Translation
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Chow, S.C.; Liu, J.P. |
Showing items 11-20 of 43 (5 Page(s) Totally) << < 1 2 3 4 5 > >> View [10|25|50] records per page
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