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Journal of Biopharmaceutical Statistics|November 27, 1999
Establishing equivalence by showing that a specified percentage of the effect of the active control over placebo is maintainedE B HolmgrenJournal of Biopharmaceutical Statistics|December 5, 2000
Progress report on the guidance for industry for statistical aspects of the design, analysis, and interpretation of chronic rodent carcinogenicity studies of pharmaceuticalsK K LinJournal of Biopharmaceutical Statistics|December 5, 2000
A modified large sample approach in the assessment of population bioequivalenceJ Quiroz, N Ting, G C Wei, et al.Journal of Biopharmaceutical Statistics|September 3, 1999
Bioequivalence review for drug interchangeabilityS C Chow, J ShaoJournal of Biopharmaceutical Statistics|December 13, 2002
On the joint analysis of longitudinal responses and early discontinuation in randomized trialsFrançois Vandenhende, Philippe LambertJournal of Biopharmaceutical Statistics|December 13, 2002
Stopping boundaries adjusted for sample size reestimation and negative stopZhenming ShunJournal of Biopharmaceutical Statistics|December 13, 2002
Tests for inter-subject and total variabilities under crossover designsYonghee Lee, Jun Shao, Shein-Chung Chow, et al.Journal of Biopharmaceutical Statistics|December 13, 2002
A decision theoretic approach to sample size determination in clinical trialsJ C Gittins, H PezeshkJournal of Biopharmaceutical Statistics|March 1, 1997
Individual bioequivalence--a European perspectiveV W Steinijans, D HauschkeJournal of Biopharmaceutical Statistics|March 1, 1997
A group sequential approach to crossover trials for average bioequivalenceW W Hauck, P E Preston, F Y BoisPageof 216