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Basic & Clinical Pharmacology & Toxicology|September 13, 2019
Modelling gastric emptying: A pharmacokinetic model simultaneously describing distribution of losartan and its active metabolite EXP-3174Eleni Karatza, Vangelis Karalis
The Journal of Pharmacy and Pharmacology|November 2, 2013
On the statistical model of the two-stage designs in bioequivalence assessmentVangelis Karalis, Panos Macheras
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|April 10, 2018
On the population pharmacokinetics and the enterohepatic recirculation of total ezetimibeKonstantina Soulele, Vangelis Karalis
Journal of Pharmaceutical Sciences|November 20, 2012
Exploring the relationships between scaled bioequivalence limits and within-subject variabilityMira Symillides, Vangelis Karalis, Panos Macheras
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|September 28, 2011
On the leveling-off properties of the new bioequivalence limits for highly variable drugs of the EMA guidelineVangelis Karalis, Mira Symillides, Panos Macheras
Pharmaceutical Research|November 24, 2004
Novel scaled average bioequivalence limits based on GMR and variability considerationsVangelis Karalis, Mira Symillides, Panos Macheras
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|June 16, 2005
Geometric mean ratio-dependent scaled bioequivalence limits with leveling-off propertiesVangelis Karalis, Panos Macheras, Mira Symillides
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|April 13, 2021
Colchicine for the treatment of COVID-19 patients: efficacy, safety, and model informed dosage regimensEleni Karatza, George Ismailos, Vangelis Karalis
Expert Opinion on Drug Metabolism & Toxicology|December 2, 2010
Novel methods to assess bioequivalenceVangelis Karalis, Mira Symillides, Panos Macheras
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|June 16, 2009
Comparison of the reference scaled bioequivalence semi-replicate method with other approaches: focus on human exposure to drugsVangelis Karalis, Mira Symillides, Panos Macheras
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