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International Journal of Pharmaceutics|August 20, 2013
The role of the upper sample size limit in two-stage bioequivalence designsVangelis KaralisExpert Opinion on Drug Metabolism & Toxicology|June 12, 2012
Current regulatory approaches of bioequivalence testingVangelis Karalis, Panos MacherasEuropean Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|May 6, 2003
Pharmacodynamic considerations in bioequivalence assessment: comparison of novel and existing metricsVangelis Karalis, Panos MacherasMaterials (Basel, Switzerland)|January 27, 2021
An In Vitro-In Vivo Simulation Approach for the Prediction of BioequivalenceMarilena Vlachou, Vangelis KaralisPharmaceutical Research|April 10, 2013
An insight into the properties of a two-stage design in bioequivalence studiesVangelis Karalis, Panos MacherasEuropean Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|August 1, 2020
Delay differential equations for the description of Irbesartan pharmacokinetics: A population approach to model absorption complexities leading to dual peaksEleni Karatza, Vangelis KaralisPharmaceutical Research|June 19, 2002
Drug disposition viewed in terms of the fractal volume of distributionVangelis Karalis, Panos MacherasInternational Journal of Pharmaceutics|January 25, 2014
A non-binary biopharmaceutical classification of drugs: the ABΓ systemPanos Macheras, Vangelis KaralisEuropean Journal of Drug Metabolism and Pharmacokinetics|March 26, 2021
Investigating the Impact of Gastric Emptying on Pharmacokinetic Parameters Using Delay Differential Equations and Principal Component AnalysisEleni Karatza, Vangelis KaralisJournal of Pharmacy & Pharmaceutical Sciences : a Publication of the Canadian Society for Pharmaceutical Sciences, Societe Canadienne Des Sciences Pharmaceutiques|September 7, 2010
Examining the role of metabolites in bioequivalence assessmentVangelis Karalis, Panos MacherasPageof 7