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Dale P Conner

Showing results (1-10 of 28) with videos related to

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The AAPS Journal|December 23, 2016
Bioavailability and Bioequivalence Aspects of Oral Modified-Release Drug ProductsRong Wang, Dale P Conner, Bing V Li
Neurology|February 28, 2002
Effect of food on absorption of Dilantin Kapseals and Mylan extended phenytoin sodium capsulesBarbara M Davit, Gur Jai Pal Singh, Dale P Conner
The AAPS Journal|October 31, 2014
Analysis of imprecision in incurred sample reanalysis for small moleculesSriram Subramaniam, Devvrat Patel, Barbara M Davit, et al.
The AAPS Journal|April 12, 2011
Dissolution testing for generic drugs: an FDA perspectiveOm Anand, Lawrence X Yu, Dale P Conner, et al.
Journal of Clinical Pharmacology|September 3, 2013
Bioequivalence study designs for generic solid oral anticancer drug products: scientific and regulatory considerationsParamjeet Kaur, Chandra S Chaurasia, Barbara M Davit, et al.
The AAPS Journal|July 4, 2013
International guidelines for bioequivalence of systemically available orally administered generic drug products: a survey of similarities and differencesBarbara Davit, April C Braddy, Dale P Conner, et al.
The AAPS Journal|October 26, 2014
Survey of international regulatory bioequivalence recommendations for approval of generic topical dermatological drug productsApril C Braddy, Barbara M Davit, Ethan M Stier, et al.
Bioanalysis|February 27, 2014
Common bioanalytical deficiencies with bioequivalence submissions in Abbreviated New Drug ApplicationsLeah N Williamson, Dale P Conner, Ethan M Stier, et al.
AAPS Pharmscitech|September 24, 2014
Biopharmaceutics classification system-based biowaivers for generic oncology drug products: case studiesNilufer Tampal, Haritha Mandula, Hongling Zhang, et al.
The AAPS Journal|January 9, 2019
Scientific Considerations for the Review and Approval of First Generic Mometasone Furoate Nasal Suspension Spray in the United States from the Bioequivalence PerspectiveQing Liu, Mohammad Absar, Bhawana Saluja, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
The AAPS Journal|December 23, 2016
Bioavailability and Bioequivalence Aspects of Oral Modified-Release Drug ProductsRong Wang, Dale P Conner, Bing V Li
Neurology|February 28, 2002
Effect of food on absorption of Dilantin Kapseals and Mylan extended phenytoin sodium capsulesBarbara M Davit, Gur Jai Pal Singh, Dale P Conner
The AAPS Journal|October 31, 2014
Analysis of imprecision in incurred sample reanalysis for small moleculesSriram Subramaniam, Devvrat Patel, Barbara M Davit, et al.
The AAPS Journal|April 12, 2011
Dissolution testing for generic drugs: an FDA perspectiveOm Anand, Lawrence X Yu, Dale P Conner, et al.
Journal of Clinical Pharmacology|September 3, 2013
Bioequivalence study designs for generic solid oral anticancer drug products: scientific and regulatory considerationsParamjeet Kaur, Chandra S Chaurasia, Barbara M Davit, et al.
The AAPS Journal|July 4, 2013
International guidelines for bioequivalence of systemically available orally administered generic drug products: a survey of similarities and differencesBarbara Davit, April C Braddy, Dale P Conner, et al.
The AAPS Journal|October 26, 2014
Survey of international regulatory bioequivalence recommendations for approval of generic topical dermatological drug productsApril C Braddy, Barbara M Davit, Ethan M Stier, et al.
Bioanalysis|February 27, 2014
Common bioanalytical deficiencies with bioequivalence submissions in Abbreviated New Drug ApplicationsLeah N Williamson, Dale P Conner, Ethan M Stier, et al.
AAPS Pharmscitech|September 24, 2014
Biopharmaceutics classification system-based biowaivers for generic oncology drug products: case studiesNilufer Tampal, Haritha Mandula, Hongling Zhang, et al.
The AAPS Journal|January 9, 2019
Scientific Considerations for the Review and Approval of First Generic Mometasone Furoate Nasal Suspension Spray in the United States from the Bioequivalence PerspectiveQing Liu, Mohammad Absar, Bhawana Saluja, et al.
Pageof 3