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The AAPS Journal|May 31, 2012
The use of modeling tools to drive efficient oral product designNeil R Mathias, John CrisonTherapeutic Delivery|October 6, 2012
Predicting feasibility and characterizing performance of extended-release formulations using physiologically based pharmacokinetic modelingJonathan Brown, John Crison, Peter TimminsAAPS Pharmscitech|November 13, 2013
Quality-by-design: are we there yet?Jack Cook, Maria T Cruañes, Manish Gupta, et al.Pharmaceutical Research|October 22, 2010
Predicting the effect of fed-state intestinal contents on drug dissolutionEce Dilber Gamsiz, Mukul Ashtikar, John Crison, et al.Journal of Pharmaceutical Sciences|November 16, 2018
Bioequivalence Comparison of Pediatric Dasatinib Formulations and Elucidation of Absorption Mechanisms Through Integrated PBPK ModelingShruthi Vaidhyanathan, Xiaoning Wang, John Crison, et al.The AAPS Journal|May 3, 2015
Food Effect in Humans: Predicting the Risk Through In Vitro Dissolution and In Vivo Pharmacokinetic ModelsNeil Mathias, Yan Xu, Balvinder Vig, et al.AAPS Pharmscitech|January 21, 2014
From bench to humans: formulation development of a poorly water soluble drug to mitigate food effectPreetanshu Pandey, Rhye Hamey, Dilbir S Bindra, et al.Molecular Pharmaceutics|November 5, 2015
Mitigation of Adverse Clinical Events of a Narrow Target Therapeutic Index Compound through Modified Release Formulation Design: An in Vitro, in Vivo, in Silico, and Clinical Pharmacokinetic AnalysisDavid J Good, Ruiling Hartley, Neil Mathias, et al.Molecular Pharmaceutics|September 17, 2013
Assessing the risk of pH-dependent absorption for new molecular entities: a novel in vitro dissolution test, physicochemical analysis, and risk assessment strategyNeil R Mathias, Yan Xu, Dhaval Patel, et al.The AAPS Journal|June 3, 2010
Meeting report: applied biopharmaceutics and quality by design for dissolution/release specification setting: product quality for patient benefitArzu Selen, Maria T Cruañes, Anette Müllertz, et al.Pageof 2