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Therapeutic Innovation & Regulatory Science|September 13, 2022
A Proposal for Post Hoc Subgroup Analysis in Support of Regulatory SubmissionJiajun Liu, Shein-Chung ChowStatistics in Medicine|December 14, 2005
On non-inferiority margin and statistical tests in active control trialsShein-Chung Chow, Jun ShaoJournal of Biopharmaceutical Statistics|July 19, 2005
Inference for clinical trials with some protocol amendmentsShein-Chung Chow, Jun ShaoOrphanet Journal of Rare Diseases|May 6, 2008
Adaptive design methods in clinical trials - a reviewShein-Chung Chow, Mark ChangJournal of Biopharmaceutical Statistics|December 13, 2016
Statistical evaluation of the scaled criterion for drug interchangeabilityJianghao Li, Shein-Chung ChowJournal of Biopharmaceutical Statistics|March 19, 2024
On the use of RWD in support of regulatory submission in drug developmentShein-Chung Chow, Peijin WangJournal of Biopharmaceutical Statistics|March 22, 2024
Analysis of innovative two-stage seamless adaptive design with different endpoints and population shiftWeijia Mai, Shein-Chung ChowJournal of Biopharmaceutical Statistics|August 28, 2019
The use of 95% CI or 90% CI for drug product development - a controversial issue?Shein-Chung Chow, Jiayin ZhengJournal of Biopharmaceutical Statistics|September 10, 2019
Criteria for dose-finding in two-stage seamless adaptive designJiayin Zheng, Shein-Chung ChowJournal of Biopharmaceutical Statistics|December 10, 2016
Assessing bioequivalence and drug interchangeabilityMeng Chen, Shein-Chung ChowPageof 150