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Pharmaceutical Statistics|March 1, 2012
A Bayesian approach to the statistical analysis of device preference studiesHaoda Fu, Yongming Qu, Baojin Zhu, et al.Pharmaceutical Statistics|September 20, 2011
An evidential approach to non-inferiority clinical trialsSue-Jane Wang, Jeffrey D BlumePharmaceutical Statistics|June 12, 2012
Extreme value modelling of laboratory safety data from clinical studiesHarry Southworth, Janet E HeffernanPharmaceutical Statistics|October 17, 2014
Adaptive graph-based multiple testing proceduresFlorian Klinglmueller, Martin Posch, Franz KoenigPharmaceutical Statistics|December 23, 2015
Predicting analysis time in events-driven clinical trials using accumulating time-to-event surrogate informationJianming Wang, Chunlei Ke, Zhinuan Yu, et al.Pharmaceutical Statistics|November 27, 2015
Nonparametric covariate adjustment in estimating hazard ratiosHonghua Jiang, Pandurang M Kulkarni, Yanping Wang, et al.Pharmaceutical Statistics|March 4, 2016
Empirical likelihood based detection procedure for change point in mean residual life functions under random censorshipYing-Ju Chen, Wei Ning, Arjun K GuptaPharmaceutical Statistics|September 29, 2015
Sample size planning for phase II trials based on success probabilities for phase IIIHeiko Götte, Armin Schüler, Marietta Kirchner, et al.Pharmaceutical Statistics|September 5, 2015
Choice of estimand and analysis methods in diabetes trials with rescue medicationBjörn Holzhauer, Mouna Akacha, Georgina BermannPharmaceutical Statistics|August 4, 2015
Bioassay case study applying the maximin D-optimal design algorithm to the four-parameter logistic modelTodd CoffeyPageof 119