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Journal of Biopharmaceutical Statistics|September 15, 2015
Some thoughts on drug interchangeabilityShein-Chung Chow, Fuyu Song, Meng ChenJournal of Biopharmaceutical Statistics|December 2, 2016
On the evaluation of reliability, repeatability, and reproducibility of instrumental evaluation methods and measurement systemsSamir Salah, Shein-Chung Chow, Fuyu SongJournal of Biopharmaceutical Statistics|December 28, 2016
On hybrid parallel-crossover designs for assessing drug interchangeability of biosimilar productsShein-Chung Chow, Fuyu Song, Can CuiJournal of Biopharmaceutical Statistics|April 29, 2025
Application of complete N-of-1 trial design in bioequivalence-biosimilar drug developmentYuqing Liu, Wendy Lou, Shein-Chung ChowJournal of Biopharmaceutical Statistics|July 31, 2002
Probability lower bounds for USP/NF testsShein-Chung Chow, Jun Shao, Hansheng WangJournal of Biopharmaceutical Statistics|December 10, 2016
Sample size requirement in analytical studies for similarity assessmentShein-Chung Chow, Fuyu Song, He BaiJournal of Biopharmaceutical Statistics|December 3, 2016
On safety margin for drug interchangeabilityJiayin Zheng, Shein-Chung Chow, Fuyu SongStatistics in Medicine|May 13, 2017
On assessing bioequivalence and interchangeability between generics based on indirect comparisonsJiayin Zheng, Shein-Chung Chow, Mengdie YuanJournal of Biopharmaceutical Statistics|December 13, 2002
A note on sample size calculation for mean comparisons based on noncentral t-statisticsShein-Chung Chow, Jun Shao, Hansheng WangJournal of Biopharmaceutical Statistics|June 2, 2012
On the independence of data monitoring committee in adaptive design clinical trialsShein-Chung Chow, Ralph Corey, Min LinPageof 150