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Showing results (121-130 of 149) with videos related to

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The AAPS Journal|September 15, 2012
Use of partial area under the curve metrics to assess bioequivalence of methylphenidate multiphasic modified release formulationsEthan M Stier, Barbara M Davit, Parthapratim Chandaroy, et al.
The AAPS Journal|October 12, 2012
Common reasons for "for-cause" inspections in bioequivalence studies submitted to the Food and Drug AdministrationBing V Li, Barbara M Davit, Christina H Lee, et al.
Investigative Ophthalmology & Visual Science|June 13, 2015
In Vivo Evaluation of White Matter Integrity and Anterograde Transport in Visual System After Excitotoxic Retinal Injury With Multimodal MRI and OCTLeon C Ho, Bo Wang, Ian P Conner, et al.
Journal of Pharmaceutical Sciences|June 21, 2024
Cellular Neonatal Fc Receptor Recycling Efficiencies can Differentiate Target-Independent Clearance Mechanisms of Monoclonal AntibodiesMark A Bryniarski, Md Tariqul Haque Tuhin, Timothy M Acker, et al.
Scientific Reports|October 4, 2019
Widespread brain reorganization perturbs visuomotor coordination in early glaucomaVivek Trivedi, Ji Won Bang, Carlos Parra, et al.
Pharmaceutical Research|August 16, 2002
Biopharmaceutics classification system: the scientific basis for biowaiver extensionsLawrence X Yu, Gordon L Amidon, James E Polli, et al.
Mabs|October 12, 2023
Utility of physiologically based pharmacokinetic modeling to predict inter-antibody variability in monoclonal antibody pharmacokinetics in miceShufang Liu, Sara C Humphreys, Kevin D Cook, et al.
The AAPS Journal|March 12, 2015
International Guidelines for Bioequivalence of Locally Acting Orally Inhaled Drug Products: Similarities and DifferencesDongmei Lu, Sau L Lee, Robert A Lionberger, et al.
Molecular Pharmaceutics|October 28, 2017
Impact of the US FDA "Biopharmaceutics Classification System" (BCS) Guidance on Global Drug DevelopmentMehul U Mehta, Ramana S Uppoor, Dale P Conner, et al.
The AAPS Journal|September 14, 2012
Implementation of a reference-scaled average bioequivalence approach for highly variable generic drug products by the US Food and Drug AdministrationBarbara M Davit, Mei-Ling Chen, Dale P Conner, et al.
Pageof 15

Showing results (121-130 of 149) with videos related to

Sort By:
Pageof 15
The AAPS Journal|September 15, 2012
Use of partial area under the curve metrics to assess bioequivalence of methylphenidate multiphasic modified release formulationsEthan M Stier, Barbara M Davit, Parthapratim Chandaroy, et al.
The AAPS Journal|October 12, 2012
Common reasons for "for-cause" inspections in bioequivalence studies submitted to the Food and Drug AdministrationBing V Li, Barbara M Davit, Christina H Lee, et al.
Investigative Ophthalmology & Visual Science|June 13, 2015
In Vivo Evaluation of White Matter Integrity and Anterograde Transport in Visual System After Excitotoxic Retinal Injury With Multimodal MRI and OCTLeon C Ho, Bo Wang, Ian P Conner, et al.
Journal of Pharmaceutical Sciences|June 21, 2024
Cellular Neonatal Fc Receptor Recycling Efficiencies can Differentiate Target-Independent Clearance Mechanisms of Monoclonal AntibodiesMark A Bryniarski, Md Tariqul Haque Tuhin, Timothy M Acker, et al.
Scientific Reports|October 4, 2019
Widespread brain reorganization perturbs visuomotor coordination in early glaucomaVivek Trivedi, Ji Won Bang, Carlos Parra, et al.
Pharmaceutical Research|August 16, 2002
Biopharmaceutics classification system: the scientific basis for biowaiver extensionsLawrence X Yu, Gordon L Amidon, James E Polli, et al.
Mabs|October 12, 2023
Utility of physiologically based pharmacokinetic modeling to predict inter-antibody variability in monoclonal antibody pharmacokinetics in miceShufang Liu, Sara C Humphreys, Kevin D Cook, et al.
The AAPS Journal|March 12, 2015
International Guidelines for Bioequivalence of Locally Acting Orally Inhaled Drug Products: Similarities and DifferencesDongmei Lu, Sau L Lee, Robert A Lionberger, et al.
Molecular Pharmaceutics|October 28, 2017
Impact of the US FDA "Biopharmaceutics Classification System" (BCS) Guidance on Global Drug DevelopmentMehul U Mehta, Ramana S Uppoor, Dale P Conner, et al.
The AAPS Journal|September 14, 2012
Implementation of a reference-scaled average bioequivalence approach for highly variable generic drug products by the US Food and Drug AdministrationBarbara M Davit, Mei-Ling Chen, Dale P Conner, et al.
Pageof 15