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Chin-Fu Hsiao

Showing results (11-20 of 147) with videos related to

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Pharmaceutical Statistics|September 2, 2020
Use of a two-sided tolerance interval in the design and evaluation of biosimilarity in clinical studiesChieh Chiang, Chi-Tian Chen, Chin-Fu Hsiao
Plos One|October 14, 2014
Sample size determination for individual bioequivalence inferenceChieh Chiang, Chin-Fu Hsiao, Jen-Pei Liu
Journal of Biopharmaceutical Statistics|October 31, 2003
A group sequential approach to evaluation of bridging studiesChin-Fu Hsiao, Jia-Zhen Xu, Jen-Pei Liu
Pharmaceutical Statistics|February 27, 2010
An alternative phase II/III design for continuous endpointsWong-Shian Huang, Jen-pei Liu, Chin-Fu Hsiao
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|November 25, 2005
Evaluation of experimental designs for two-color cDNA microarraysChu-Wen Yang, Chin-Fu Hsiao, Chen-Kung Chou
Journal of Biopharmaceutical Statistics|February 11, 2005
A two-stage design for bridging studiesChin-Fu Hsiao, Jia-Zhen Xu, Jen-Pei Liu
Journal of Biopharmaceutical Statistics|September 6, 2012
Design and evaluation of multiregional trials with heterogeneous treatment effect across regionsChi-Tian Chen, H M James Hung, Chin-Fu Hsiao
Plos One|July 1, 2017
Sample size determination for a specific region in multiregional clinical trials with multiple co-primary endpointsWong-Shian Huang, Hui-Nien Hung, Toshimitsu Hamasaki, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|January 9, 2009
Current advanced statistical issues in clinical research---adaptive designs and translational medicineChin-Fu Hsiao, Tsang-Wu Walter Liu, Chih-Hsin James Yang
Journal of Biopharmaceutical Statistics|September 6, 2012
Statistical methods for bridging studiesShein-Chung Chow, Chieh Chiang, Jen-pei Liu, et al.
Pageof 15

Showing results (11-20 of 147) with videos related to

Sort By:
Pageof 15
Pharmaceutical Statistics|September 2, 2020
Use of a two-sided tolerance interval in the design and evaluation of biosimilarity in clinical studiesChieh Chiang, Chi-Tian Chen, Chin-Fu Hsiao
Plos One|October 14, 2014
Sample size determination for individual bioequivalence inferenceChieh Chiang, Chin-Fu Hsiao, Jen-Pei Liu
Journal of Biopharmaceutical Statistics|October 31, 2003
A group sequential approach to evaluation of bridging studiesChin-Fu Hsiao, Jia-Zhen Xu, Jen-Pei Liu
Pharmaceutical Statistics|February 27, 2010
An alternative phase II/III design for continuous endpointsWong-Shian Huang, Jen-pei Liu, Chin-Fu Hsiao
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|November 25, 2005
Evaluation of experimental designs for two-color cDNA microarraysChu-Wen Yang, Chin-Fu Hsiao, Chen-Kung Chou
Journal of Biopharmaceutical Statistics|February 11, 2005
A two-stage design for bridging studiesChin-Fu Hsiao, Jia-Zhen Xu, Jen-Pei Liu
Journal of Biopharmaceutical Statistics|September 6, 2012
Design and evaluation of multiregional trials with heterogeneous treatment effect across regionsChi-Tian Chen, H M James Hung, Chin-Fu Hsiao
Plos One|July 1, 2017
Sample size determination for a specific region in multiregional clinical trials with multiple co-primary endpointsWong-Shian Huang, Hui-Nien Hung, Toshimitsu Hamasaki, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|January 9, 2009
Current advanced statistical issues in clinical research---adaptive designs and translational medicineChin-Fu Hsiao, Tsang-Wu Walter Liu, Chih-Hsin James Yang
Journal of Biopharmaceutical Statistics|September 6, 2012
Statistical methods for bridging studiesShein-Chung Chow, Chieh Chiang, Jen-pei Liu, et al.
Pageof 15