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Pharmaceutical Research|April 6, 2002
Determination of in vivo bioequivalenceAndre J Jackson
Clinical Pharmacokinetics|July 13, 2004
Metabolites and bioequivalence: past and presentAndre J Jackson, Gabriel Robbie, Patrick Marroum
Journal of Clinical Pharmacology|September 25, 2010
Bioavailability considerations in evaluating drug-drug interactions using the population pharmacokinetic approachJohn Z Duan, Andre J Jackson, Ping Zhao
Pharmaceutical Research|September 26, 2012
Use of partial AUC (PAUC) to evaluate bioequivalence--a case study with complex absorption: methylphenidateJeanne Fourie Zirkelbach, Andre J Jackson, Yaning Wang, et al.
Journal of Pharmaceutical Sciences|August 29, 2012
Bioequivalence of long half-life drugs--informative sampling determination--using truncated area in parallel-designed studies for slow sustained-release formulationsAhmed El-Tahtawy, Ferrin Harrison, Jeanne Fourie Zirkelbach, et al.
Theoretical Biology & Medical Modelling|September 4, 2012
Individualized, discrete event, simulations provide insight into inter- and intra-subject variability of extended-release, drug productsSean H J Kim, Andre J Jackson, Rim Hur, et al.
The Journal of Clinical Psychiatry|January 7, 2015
The US Food and Drug Administration's perspective on the new antidepressant vortioxetineJing Zhang, Mitchell V Mathis, Jenn W Sellers, et al.
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