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E Diletti

Showing results (1-10 of 21) with videos related to

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European Journal of Clinical Pharmacology|January 1, 1985
Generalization of distribution--free confidence intervals for bioavailability ratiosV W Steinijans, E Diletti
European Journal of Clinical Pharmacology|January 1, 1983
Statistical analysis of bioavailability studies: parametric and nonparametric confidence intervalsV W Steinijans, E Diletti
International Journal of Clinical Pharmacology, Therapy, and Toxicology|February 1, 1990
A distribution-free procedure for the statistical analysis of bioequivalence studiesD Hauschke, V W Steinijans, E Diletti
International Journal of Clinical Pharmacology, Therapy, and Toxicology|January 1, 1992
Sample size determination: extended tables for the multiplicative model and bioequivalence ranges of 0.9 to 1.11 and 0.7 to 1.43E Diletti, D Hauschke, V W Steinijans
International 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 Diletti
International 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 Steinijans
International 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 Steinijans
International Journal of Clinical Pharmacology, Therapy, and Toxicology|August 1, 1992
Sample size determination: extended tables for the multiplicative model and bioequivalence ranges of 0.9 to 1.11 and 0.7 to 1.43E Diletti, D Hauschke, V W Steinijans
Arzneimittel-Forschung|August 1, 1988
Validation of the in-vitro dissolution method used for a new sustained-release theophylline pellet formulationR Dietrich, R Brausse, A Bautz, et al.
Statistics 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.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
European Journal of Clinical Pharmacology|January 1, 1985
Generalization of distribution--free confidence intervals for bioavailability ratiosV W Steinijans, E Diletti
European Journal of Clinical Pharmacology|January 1, 1983
Statistical analysis of bioavailability studies: parametric and nonparametric confidence intervalsV W Steinijans, E Diletti
International Journal of Clinical Pharmacology, Therapy, and Toxicology|February 1, 1990
A distribution-free procedure for the statistical analysis of bioequivalence studiesD Hauschke, V W Steinijans, E Diletti
International Journal of Clinical Pharmacology, Therapy, and Toxicology|January 1, 1992
Sample size determination: extended tables for the multiplicative model and bioequivalence ranges of 0.9 to 1.11 and 0.7 to 1.43E Diletti, D Hauschke, V W Steinijans
International 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 Diletti
International 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 Steinijans
International 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 Steinijans
International Journal of Clinical Pharmacology, Therapy, and Toxicology|August 1, 1992
Sample size determination: extended tables for the multiplicative model and bioequivalence ranges of 0.9 to 1.11 and 0.7 to 1.43E Diletti, D Hauschke, V W Steinijans
Arzneimittel-Forschung|August 1, 1988
Validation of the in-vitro dissolution method used for a new sustained-release theophylline pellet formulationR Dietrich, R Brausse, A Bautz, et al.
Statistics 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.
Pageof 3