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Barbara Davit

Showing results (1-10 of 11) with videos related to

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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.
Neurology|March 27, 2016
Assessing bioequivalence of generic modified-release antiepileptic drugsEmily L Johnson, Yi-Ting Chang, Barbara Davit, et al.
Pharmaceutical Research|April 14, 2011
Using partial area for evaluation of bioavailability and bioequivalenceMei-Ling Chen, Barbara Davit, Robert Lionberger, et al.
The AAPS Journal|August 30, 2008
Evaluation of a scaling approach for the bioequivalence of highly variable drugsSam H Haidar, Fairouz Makhlouf, Donald J Schuirmann, et al.
International Journal of Pharmaceutics|May 13, 2017
Food effects in paediatric medicines development for products Co-administered with foodHannah Batchelor, Ann Marie Kaukonen, Sandra Klein, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|October 2, 2017
The Global Bioequivalence Harmonization Initiative: Summary report for EUFEPS international conferenceMei-Ling Chen, Henning Blume, Gerald Beuerle, et al.
Pharmaceutical Research|September 25, 2007
Bioequivalence approaches for highly variable drugs and drug productsSam H Haidar, Barbara Davit, Mei-Ling Chen, et al.
Pharmaceutical Research|January 8, 2014
Current challenges in bioequivalence, quality, and novel assessment technologies for topical productsAvraham Yacobi, Vinod P Shah, Edward D Bashaw, et al.
Clinical Therapeutics|January 4, 2011
Challenges and opportunities in establishing scientific and regulatory standards for determining therapeutic equivalence of modified-release products: Workshop summary reportMei-Ling Chen, Vinod P Shah, Derek Ganes, et al.
The AAPS Journal|May 5, 2010
Challenges and opportunities in establishing scientific and regulatory standards for assuring therapeutic equivalence of modified release products: workshop summary reportMei-Ling Chen, Vinod P Shah, Derek Ganes, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
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.
Neurology|March 27, 2016
Assessing bioequivalence of generic modified-release antiepileptic drugsEmily L Johnson, Yi-Ting Chang, Barbara Davit, et al.
Pharmaceutical Research|April 14, 2011
Using partial area for evaluation of bioavailability and bioequivalenceMei-Ling Chen, Barbara Davit, Robert Lionberger, et al.
The AAPS Journal|August 30, 2008
Evaluation of a scaling approach for the bioequivalence of highly variable drugsSam H Haidar, Fairouz Makhlouf, Donald J Schuirmann, et al.
International Journal of Pharmaceutics|May 13, 2017
Food effects in paediatric medicines development for products Co-administered with foodHannah Batchelor, Ann Marie Kaukonen, Sandra Klein, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|October 2, 2017
The Global Bioequivalence Harmonization Initiative: Summary report for EUFEPS international conferenceMei-Ling Chen, Henning Blume, Gerald Beuerle, et al.
Pharmaceutical Research|September 25, 2007
Bioequivalence approaches for highly variable drugs and drug productsSam H Haidar, Barbara Davit, Mei-Ling Chen, et al.
Pharmaceutical Research|January 8, 2014
Current challenges in bioequivalence, quality, and novel assessment technologies for topical productsAvraham Yacobi, Vinod P Shah, Edward D Bashaw, et al.
Clinical Therapeutics|January 4, 2011
Challenges and opportunities in establishing scientific and regulatory standards for determining therapeutic equivalence of modified-release products: Workshop summary reportMei-Ling Chen, Vinod P Shah, Derek Ganes, et al.
The AAPS Journal|May 5, 2010
Challenges and opportunities in establishing scientific and regulatory standards for assuring therapeutic equivalence of modified release products: workshop summary reportMei-Ling Chen, Vinod P Shah, Derek Ganes, et al.
Pageof 2