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Journal of Biopharmaceutical Statistics|October 31, 2014
Analytical procedure validation and the quality by design paradigmEric Rozet, Pierre Lebrun, Jean-François Michiels, et al.Journal of Biopharmaceutical Statistics|October 31, 2014
Dissolution curve comparisons through the F(2) parameter, a Bayesian extension of the f(2) statisticSteven Novick, Yan Shen, Harry Yang, et al.Journal of Biopharmaceutical Statistics|October 31, 2014
Statistical considerations in setting product specificationsXiaoyu Dong, Yi Tsong, Meiyu ShenJournal of Biopharmaceutical Statistics|November 8, 2014
Optimal Futility Interim Design: A Predictive Probability of Success Approach with Time-to-Event EndpointZhongwen TangJournal of Biopharmaceutical Statistics|February 17, 2016
A curve-free Bayesian decision-theoretic design for two-agent Phase I trialsBee L Lee, Shenghua K Fan, Ying LuJournal of Biopharmaceutical Statistics|October 22, 2014
Statistical Perspectives on Subgroup Analysis: Testing for Heterogeneity and Evaluating Error Rate for the Complementary SubgroupMohamed Alosh, Mohammad F Huque, Gary G KochJournal of Biopharmaceutical Statistics|October 17, 2014
Group Sequential Design for Randomized Phase III Trials under the Weibull ModelJianrong Wu, Xiaoping XiongJournal of Biopharmaceutical Statistics|October 17, 2014
A Simple Approach for Sample Size Calculation for Comparing Two Concordance Correlation Coefficients Estimated on the Same SubjectsHung-Mo Lin, John M WilliamsonJournal of Biopharmaceutical Statistics|December 2, 2014
Hypoglycemic events analysis via recurrent time-to-event (HEART) modelsHaoda Fu, Junxiang Luo, Yongming QuJournal of Biopharmaceutical Statistics|November 6, 2014
A simple and flexible graphical approach for adaptive group-sequential clinical trialsToshifumi Sugitani, Frank Bretz, Willi MaurerPageof 216