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Pharmaceutical Statistics|July 16, 2015
Carryover negligibility and relevance in bioequivalence studiesJordi Ocaña, Maria P Sanchez O, Josep L CarrascoPharmaceutical Statistics|April 21, 2015
A novel test to compare two treatments based on endpoints involving both nonfatal and fatal eventsRichard F Potthoff, Susan HalabiPharmaceutical Statistics|August 4, 2016
A generalized analytic solution to the win ratio to analyze a composite endpoint considering the clinical importance order among componentsGaohong Dong, Di Li, Steffen Ballerstedt, et al.Pharmaceutical Statistics|June 3, 2015
A Bayesian estimate of the concordance correlation coefficient with skewed dataDai Feng, Richard Baumgartner, Vladimir SvetnikPharmaceutical Statistics|September 20, 2007
A unifying approach to non-inferiority, equivalence and superiority tests via multiple decision processesChihiro HirotsuPharmaceutical Statistics|September 20, 2007
The difficult and ubiquitous problems of multiplicitiesDonald A BerryPharmaceutical Statistics|May 26, 2007
Methods for one-sided testing of the difference between proportions and sample size considerations related to non-inferiority clinical trialsRebekkah S Dann, Gary G KochPharmaceutical Statistics|February 22, 2007
Nonparametric empirical Bayes method for comparison of treatment effects with application to stress urinary incontinence dataChaofeng Liu, Wei Shen, Jun XiePharmaceutical Statistics|January 19, 2007
Analysis of exacerbation rates in asthma and chronic obstructive pulmonary disease: example from the TRISTAN studyOliver N Keene, Mark R K Jones, Peter W Lane, et al.Pharmaceutical Statistics|August 22, 2007
Sequential design approaches for bioequivalence studies with crossover designsDiane Potvin, Charles E DiLiberti, Walter W Hauck, et al.Pageof 119