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Robert A Lionberger

Showing results (1-10 of 19) with videos related to

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Clinical Pharmacology and Therapeutics|January 17, 2019
Innovation for Generic Drugs: Science and Research Under the Generic Drug User Fee Amendments of 2012Robert A Lionberger
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|August 22, 2002
Viscosity of bimodal and polydisperse colloidal suspensionsRobert A Lionberger
The AAPS Journal|May 1, 2008
FDA critical path initiatives: opportunities for generic drug developmentRobert A Lionberger
Clinical Pharmacology and Therapeutics|January 17, 2020
Generics 2030: Where Are We Heading in 2030 for Generic Drug Science, Research, and Regulation?Lei Zhang, Robert A Lionberger
The AAPS Journal|May 18, 2016
Clinical, Pharmacokinetic, and In Vitro Studies to Support Bioequivalence of Ophthalmic Drug ProductsStephanie H Choi, Robert A Lionberger
Molecular Pharmaceutics|July 21, 2005
Impact of P-glycoprotein-mediated intestinal efflux kinetics on oral bioavailability of P-glycoprotein substratesHyojong Kwon, Robert A Lionberger, Lawrence X Yu
Therapeutic Delivery|June 7, 2013
Innovative approaches for demonstration of bioequivalence: the US FDA perspectiveXinyuan Zhang, Nan Zheng, Robert A Lionberger, et al.
The AAPS Journal|January 6, 2011
Utility of physiologically based absorption modeling in implementing Quality by Design in drug developmentXinyuan Zhang, Robert A Lionberger, Barbara M Davit, et al.
The AAPS Journal|May 10, 2008
Quality by design: concepts for ANDAsRobert A Lionberger, Sau Lawrence Lee, Laiming Lee, et al.
Pharmaceutical Research|January 27, 2012
Use of partial AUC to demonstrate bioequivalence of Zolpidem Tartrate Extended Release formulationsRobert A Lionberger, Andre S Raw, Stephanie H Kim, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Clinical Pharmacology and Therapeutics|January 17, 2019
Innovation for Generic Drugs: Science and Research Under the Generic Drug User Fee Amendments of 2012Robert A Lionberger
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|August 22, 2002
Viscosity of bimodal and polydisperse colloidal suspensionsRobert A Lionberger
The AAPS Journal|May 1, 2008
FDA critical path initiatives: opportunities for generic drug developmentRobert A Lionberger
Clinical Pharmacology and Therapeutics|January 17, 2020
Generics 2030: Where Are We Heading in 2030 for Generic Drug Science, Research, and Regulation?Lei Zhang, Robert A Lionberger
The AAPS Journal|May 18, 2016
Clinical, Pharmacokinetic, and In Vitro Studies to Support Bioequivalence of Ophthalmic Drug ProductsStephanie H Choi, Robert A Lionberger
Molecular Pharmaceutics|July 21, 2005
Impact of P-glycoprotein-mediated intestinal efflux kinetics on oral bioavailability of P-glycoprotein substratesHyojong Kwon, Robert A Lionberger, Lawrence X Yu
Therapeutic Delivery|June 7, 2013
Innovative approaches for demonstration of bioequivalence: the US FDA perspectiveXinyuan Zhang, Nan Zheng, Robert A Lionberger, et al.
The AAPS Journal|January 6, 2011
Utility of physiologically based absorption modeling in implementing Quality by Design in drug developmentXinyuan Zhang, Robert A Lionberger, Barbara M Davit, et al.
The AAPS Journal|May 10, 2008
Quality by design: concepts for ANDAsRobert A Lionberger, Sau Lawrence Lee, Laiming Lee, et al.
Pharmaceutical Research|January 27, 2012
Use of partial AUC to demonstrate bioequivalence of Zolpidem Tartrate Extended Release formulationsRobert A Lionberger, Andre S Raw, Stephanie H Kim, et al.
Pageof 2