Showing results (1451-1460 of 2,158) with videos related to
Sort By:
Pageof 216
Journal of Biopharmaceutical Statistics|January 6, 2017
Exact test-based approach for equivalence test with parameter marginXiaoyu Cassie Dong, Yuanyuan Bian, Yi Tsong, et al.Journal of Biopharmaceutical Statistics|December 2, 2016
Statistical considerations regarding correlated lots in analytical biosimilar equivalence testMeiyu Shen, Tianhua Wang, Yi TsongJournal of Biopharmaceutical Statistics|December 2, 2016
On the evaluation of reliability, repeatability, and reproducibility of instrumental evaluation methods and measurement systemsSamir Salah, Shein-Chung Chow, Fuyu SongJournal of Biopharmaceutical Statistics|December 28, 2016
On hybrid parallel-crossover designs for assessing drug interchangeability of biosimilar productsShein-Chung Chow, Fuyu Song, Can CuiJournal of Biopharmaceutical Statistics|April 5, 2014
Influence of covariance between random effects in design for nonlinear mixed-effect models with an illustration in pediatric pharmacokineticsCyrielle Dumont, Marylore Chenel, France MentréJournal of Biopharmaceutical Statistics|April 5, 2014
Phase II design with sequential testing of hypotheses within each stageStavroula Poulopoulou, Dimitris Karlis, Constantin T Yiannoutsos, et al.Journal of Biopharmaceutical Statistics|April 5, 2014
Impact of subject attrition on sample size determinations for longitudinal cluster randomized clinical trialsMoonseong HeoJournal of Biopharmaceutical Statistics|April 5, 2014
Confidence-interval construction for rate ratio in matched-pair studies with incomplete dataHui-Qiong Li, Ivan S F Chan, Man-Lai Tang, et al.Journal of Biopharmaceutical Statistics|January 1, 1991
The estimation of parameters from bulked samplesS C Chow, E V NordheimJournal of Biopharmaceutical Statistics|January 1, 1991
Situations where formal confirmatory analysis is inappropriate for clinical researchD SalsburgPageof 216