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Journal of Biopharmaceutical Statistics|June 22, 2013
Evaluating the performance of the ICH guidelines for shelf life estimationMichelle Quinlan, Walter Stroup, James Schwenke, et al.Journal of Biopharmaceutical Statistics|June 22, 2013
Medical records-based postmarketing safety evaluation of rare events with uncertain statusHongyuan Cao, Lisa M LaVange, Joseph F Heyse, et al.Journal of Biopharmaceutical Statistics|June 27, 2013
Three-arm noninferiority trials with a prespecified margin for inference of the difference in the proportions of binary endpointsEisuke Hida, Toshiro TangoJournal of Biopharmaceutical Statistics|August 21, 2013
Optimal timing for interim analyses in clinical trialsKanae Togo, Manabu IwasakiJournal of Biopharmaceutical Statistics|August 21, 2013
Evaluating and adjusting for premature censoring of progression-free survivalMark Rothmann, Kallappa Koti, Kyung Yul Lee, et al.Journal of Biopharmaceutical Statistics|August 21, 2013
A comparison of bias-corrected covariance estimators for generalized estimating equationsChunpeng Fan, Donghui Zhang, Cun-Hui ZhangJournal of Biopharmaceutical Statistics|February 20, 2016
Multiple contrast type tests for the evaluation of animal carcinogenicity studiesMohammad Rahman, Ram TiwariJournal of Biopharmaceutical Statistics|February 20, 2016
Group-sequential three-arm noninferiority clinical trial designsToshimitsu Ochiai, Toshimitsu Hamasaki, Scott R Evans, et al.Journal of Biopharmaceutical Statistics|February 17, 2016
Sample size determination with familywise control of both type I and type II errors in clinical trialsBushi Wang, Naitee TingJournal of Biopharmaceutical Statistics|February 17, 2016
Novel dose-finding designs and considerations on practical implementations in oncology clinical trialsBo Huang, Paul Bycott, Enayet TalukderPageof 216