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Statistics in Medicine|January 11, 2017
An approach for sample size determination of average bioequivalence based on interval estimationChieh Chiang, Chin-Fu HsiaoStatistical Methods in Medical Research|January 23, 2018
Use of interval estimations in design and evaluation of multiregional clinical trials with continuous outcomesChieh Chiang, Chin-Fu HsiaoPlos One|February 5, 2021
Tolerance interval testing for assessing accuracy and precision simultaneouslyChieh Chiang, Chin-Fu HsiaoPharmaceutical 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 HsiaoPlos One|October 14, 2014
Sample size determination for individual bioequivalence inferenceChieh Chiang, Chin-Fu Hsiao, Jen-Pei LiuJournal of Biopharmaceutical Statistics|September 6, 2012
Statistical methods for bridging studiesShein-Chung Chow, Chieh Chiang, Jen-pei Liu, et al.Statistics in Biopharmaceutical Research|June 30, 2021
Operational Experiences in China and Statistical Issues on the Conduct of Clinical Trials During the COVID-19 PandemicTong Guo, Chian Chen, Chieh Chiang, et al.Statistics in Medicine|October 27, 2021
Use of likelihood estimates for variances for the design and evaluation of multiregional clinical trials with heterogeneous variancesYuh-Jenn Wu, Yu-Chieh Cheng, Chieh Chiang, et al.Journal of Biopharmaceutical Statistics|May 13, 2020
Use of a tolerance interval approach as a statistical quality control tool for traditional Chinese medicineChieh Chiang, Yi-Hsuan Lai, Bo-Han Huang, et al.Statistics in Medicine|August 6, 2020
Use of tolerance intervals for assessing biosimilarityChian Chen, Chin-Fu HsiaoPageof 25