Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Pharmaceutical Statistics|April 14, 2015
Advantages of a wholly Bayesian approach to assessing efficacy in early drug development: a case studyRosalind J Walley, Claire L Smith, Jeremy D Gale, et al.
Pharmaceutical Statistics|September 3, 2016
Simulation-based sample-sizing and power calculations in logistic regression with partial prior informationAndrew P Grieve, Shah-Jalal Sarker
Biometrical Journal. Biometrische Zeitschrift|March 23, 2016
The predictive distribution of the residual variability in the linear-fixed effects model for clinical cross-over trialsAnja Bertsche, Gerhard Nehmiz, Jan Beyersmann, et al.
Journal of Clinical Epidemiology|December 27, 2011
Within-person study designs had lower precision and greater susceptibility to bias because of trends in exposure than cohort and nested case-control designsJennifer M Nicholas, Andrew P Grieve, Martin C Gulliford
Journal of Biopharmaceutical Statistics|November 21, 2007
Flexible design and efficient implementation of adaptive dose-finding studiesChristopher J Weir, David J Spiegelhalter, Andrew P Grieve
Journal of Chemical Information and Modeling|October 9, 2007
Designing compound subsets: comparison of random and rational approaches using statistical simulationSiew Kuen Yeap, Rosalind J Walley, Mike Snarey, et al.
Pharmaceutical Statistics|February 17, 2017
Statistical issues in first-in-human studies on BIA 10-2474: Neglected comparison of protocol against practiceSheila M Bird, Rosemary A Bailey, Andrew P Grieve, et al.
Pharmaceutical Statistics|November 4, 2006
Implementation of a Bayesian adaptive design in a proof of concept studyMichael K Smith, Ieuan Jones, Mark F Morris, et al.
Pageof 3