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Shein Chung Chow

Showing results (61-70 of 192) with videos related to

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Journal of Biopharmaceutical Statistics|April 29, 2025
Application of complete N-of-1 trial design in bioequivalence-biosimilar drug developmentYuqing Liu, Wendy Lou, Shein-Chung Chow
Journal of Biopharmaceutical Statistics|July 31, 2002
Probability lower bounds for USP/NF testsShein-Chung Chow, Jun Shao, Hansheng Wang
Journal of Biopharmaceutical Statistics|December 10, 2016
Sample size requirement in analytical studies for similarity assessmentShein-Chung Chow, Fuyu Song, He Bai
Journal of Biopharmaceutical Statistics|December 3, 2016
On safety margin for drug interchangeabilityJiayin Zheng, Shein-Chung Chow, Fuyu Song
Journal of Biopharmaceutical Statistics|May 13, 2008
On power and sample size calculation for QT studies with recording replicates at given time pointShein-Chung Chow, Bin Cheng, Dennis Cosmatos
Statistics in Medicine|May 13, 2017
On assessing bioequivalence and interchangeability between generics based on indirect comparisonsJiayin Zheng, Shein-Chung Chow, Mengdie Yuan
Journal 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 Wang
Journal of Biopharmaceutical Statistics|June 2, 2012
On the independence of data monitoring committee in adaptive design clinical trialsShein-Chung Chow, Ralph Corey, Min Lin
Statistics in Medicine|May 19, 2005
Statistical inference for cancer trials with treatment switchingJun Shao, Mark Chang, Shein-Chung Chow
Journal of Biopharmaceutical Statistics|April 12, 2025
The role of regulatory flexibility in the review and approval process of rare disease drug developmentShein-Chung Chow, Anne Pariser, Steven Galson
Pageof 20

Showing results (61-70 of 192) with videos related to

Sort By:
Pageof 20
Journal of Biopharmaceutical Statistics|April 29, 2025
Application of complete N-of-1 trial design in bioequivalence-biosimilar drug developmentYuqing Liu, Wendy Lou, Shein-Chung Chow
Journal of Biopharmaceutical Statistics|July 31, 2002
Probability lower bounds for USP/NF testsShein-Chung Chow, Jun Shao, Hansheng Wang
Journal of Biopharmaceutical Statistics|December 10, 2016
Sample size requirement in analytical studies for similarity assessmentShein-Chung Chow, Fuyu Song, He Bai
Journal of Biopharmaceutical Statistics|December 3, 2016
On safety margin for drug interchangeabilityJiayin Zheng, Shein-Chung Chow, Fuyu Song
Journal of Biopharmaceutical Statistics|May 13, 2008
On power and sample size calculation for QT studies with recording replicates at given time pointShein-Chung Chow, Bin Cheng, Dennis Cosmatos
Statistics in Medicine|May 13, 2017
On assessing bioequivalence and interchangeability between generics based on indirect comparisonsJiayin Zheng, Shein-Chung Chow, Mengdie Yuan
Journal 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 Wang
Journal of Biopharmaceutical Statistics|June 2, 2012
On the independence of data monitoring committee in adaptive design clinical trialsShein-Chung Chow, Ralph Corey, Min Lin
Statistics in Medicine|May 19, 2005
Statistical inference for cancer trials with treatment switchingJun Shao, Mark Chang, Shein-Chung Chow
Journal of Biopharmaceutical Statistics|April 12, 2025
The role of regulatory flexibility in the review and approval process of rare disease drug developmentShein-Chung Chow, Anne Pariser, Steven Galson
Pageof 20