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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 differences
Barbara Davit, April C Braddy, Dale P Conner, et al.
Neurology
|
March 27, 2016
Assessing bioequivalence of generic modified-release antiepileptic drugs
Emily L Johnson, Yi-Ting Chang, Barbara Davit, et al.
Pharmaceutical Research
|
April 14, 2011
Using partial area for evaluation of bioavailability and bioequivalence
Mei-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 drugs
Sam 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 food
Hannah 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 conference
Mei-Ling Chen, Henning Blume, Gerald Beuerle, et al.
Pharmaceutical Research
|
September 25, 2007
Bioequivalence approaches for highly variable drugs and drug products
Sam 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 products
Avraham 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 report
Mei-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 report
Mei-Ling Chen, Vinod P Shah, Derek Ganes, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
The AAPS Journal
|
July 4, 2013
International guidelines for bioequivalence of systemically available orally administered generic drug products: a survey of similarities and differences
Barbara Davit, April C Braddy, Dale P Conner, et al.
Neurology
|
March 27, 2016
Assessing bioequivalence of generic modified-release antiepileptic drugs
Emily L Johnson, Yi-Ting Chang, Barbara Davit, et al.
Pharmaceutical Research
|
April 14, 2011
Using partial area for evaluation of bioavailability and bioequivalence
Mei-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 drugs
Sam 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 food
Hannah 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 conference
Mei-Ling Chen, Henning Blume, Gerald Beuerle, et al.
Pharmaceutical Research
|
September 25, 2007
Bioequivalence approaches for highly variable drugs and drug products
Sam 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 products
Avraham 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 report
Mei-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 report
Mei-Ling Chen, Vinod P Shah, Derek Ganes, et al.
Page
of 2