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International Journal of Clinical Pharmacology, Therapy, and Toxicology|July 1, 1992
Presentation of results from bioequivalence studiesR Sauter, V W Steinijans, E Diletti, et al.International Journal of Clinical Pharmacology, Therapy, and Toxicology|December 1, 1992
Effect of changing the bioequivalence range from (0.80, 1.20) to (0.80, 1.25) on the power and sample sizeV W Steinijans, W W Hauck, E Diletti, et al.International Journal of Clinical Pharmacology, Therapy, and Toxicology|January 1, 1992
Presentation of results from bioequivalence studiesR Sauter, V W Steinijans, E Diletti, et al.Journal of Biopharmaceutical Statistics|March 1, 1997
Choice of student's t- or Wilcoxon-based confidence intervals for assessment of average bioequivalenceW W Hauck, D Hauschke, E Diletti, et al.European Journal of Drug Metabolism and Pharmacokinetics|April 1, 1990
Pharmacokinetic characterization of controlled-release formulationsV W SteinijansJournal of Biopharmaceutical Statistics|March 1, 1997
Individual bioequivalence--a European perspectiveV W Steinijans, D HauschkeChronobiology International|January 1, 1987
Therapeutic advantage of unequal dosing of theophylline in patients with nocturnal asthmaP Dorow, V W SteinijansInternational 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The U.S. draft guidance regarding population and individual bioequivalence approaches: comments by a research-based pharmaceutical companyD Hauschke, V W SteinijansInternational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 HauschkePageof 11