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Journal of Biopharmaceutical Statistics|November 27, 1999
Approximate sample sizes for testing hypotheses about the ratio and difference of two meansM Kieser, D HauschkeStatistics in Medicine|February 17, 1999
Sample size determination for proving equivalence based on the ratio of two means for normally distributed dataD Hauschke, M Kieser, E Diletti, et al.Journal of Biopharmaceutical Statistics|March 1, 1997
Individual bioequivalence--a European perspectiveV W Steinijans, D HauschkeInternational Journal of Clinical Pharmacology, Therapy, and Toxicology|March 1, 1990
Update on the statistical analysis of bioequivalence studiesV W Steinijans, D HauschkeStatistics in Medicine|October 18, 2000
The U.S. draft guidance regarding population and individual bioequivalence approaches: comments by a research-based pharmaceutical companyD Hauschke, V W SteinijansInternational Journal of Clinical Pharmacology, Therapy, and Toxicology|January 1, 1992
Update on the statistical analysis of bioequivalence studiesV W Steinijans, D HauschkeJournal of Biopharmaceutical Statistics|March 10, 2000
Identifying the maximum safe dose: a multiple testing approachL A Hothorn, D HauschkeInternational Journal of Clinical Pharmacology, Therapy, and Toxicology|January 1, 1992
A distribution-free procedure for the statistical analysis of bioequivalence studiesD Hauschke, V W Steinijans, E DilettiInternational Journal of Clinical Pharmacology, Therapy, and Toxicology|January 1, 1991
Sample size determination for bioequivalence assessment by means of confidence intervalsE Diletti, D Hauschke, V W SteinijansInternational Journal of Clinical Pharmacology, Therapy, and Toxicology|January 1, 1992
Sample size determination for bioequivalence assessment by means of confidence intervalsE Diletti, D Hauschke, V W SteinijansPageof 17