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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 formulations
Ethan 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 Administration
Bing V Li, Barbara M Davit, Christina H Lee, et al.
Pharmaceutical Research
|
August 16, 2002
Biopharmaceutics classification system: the scientific basis for biowaiver extensions
Lawrence X Yu, Gordon L Amidon, James E Polli, et al.
The AAPS Journal
|
March 12, 2015
International Guidelines for Bioequivalence of Locally Acting Orally Inhaled Drug Products: Similarities and Differences
Dongmei 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 Development
Mehul 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 Administration
Barbara M Davit, Mei-Ling Chen, Dale P Conner, et al.
Journal of Aerosol Medicine and Pulmonary Drug Delivery
|
February 6, 2010
Demonstrating Bioequivalence of Locally Acting Orally Inhaled Drug Products (OIPs): Workshop Summary Report
Wallace P Adams, Richard C Ahrens, Mei-Ling Chen, et al.
Journal of Pharmaceutical Sciences
|
May 5, 2004
Summary workshop report: biopharmaceutics classification system--implementation challenges and extension opportunities
James E Polli, Lawrence X Yu, Jack A Cook, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 28) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 28 results.
The AAPS Journal
|
September 15, 2012
Use of partial area under the curve metrics to assess bioequivalence of methylphenidate multiphasic modified release formulations
Ethan 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 Administration
Bing V Li, Barbara M Davit, Christina H Lee, et al.
Pharmaceutical Research
|
August 16, 2002
Biopharmaceutics classification system: the scientific basis for biowaiver extensions
Lawrence X Yu, Gordon L Amidon, James E Polli, et al.
The AAPS Journal
|
March 12, 2015
International Guidelines for Bioequivalence of Locally Acting Orally Inhaled Drug Products: Similarities and Differences
Dongmei 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 Development
Mehul 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 Administration
Barbara M Davit, Mei-Ling Chen, Dale P Conner, et al.
Journal of Aerosol Medicine and Pulmonary Drug Delivery
|
February 6, 2010
Demonstrating Bioequivalence of Locally Acting Orally Inhaled Drug Products (OIPs): Workshop Summary Report
Wallace P Adams, Richard C Ahrens, Mei-Ling Chen, et al.
Journal of Pharmaceutical Sciences
|
May 5, 2004
Summary workshop report: biopharmaceutics classification system--implementation challenges and extension opportunities
James E Polli, Lawrence X Yu, Jack A Cook, et al.
Page
of 3