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The AAPS Journal|October 31, 2014
Analysis of imprecision in incurred sample reanalysis for small moleculesSriram Subramaniam, Devvrat Patel, Barbara M Davit, 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|April 12, 2011
Dissolution testing for generic drugs: an FDA perspectiveOm Anand, Lawrence X Yu, Dale P Conner, 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.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.Dermatologic Therapy|May 21, 2009
Generic drugs--safe, effective, and affordableJohn R Peters, Dena R Hixon, Dale P Conner, et al.International Journal of Pharmaceutics|August 2, 2011
The role of predictive biopharmaceutical modeling and simulation in drug development and regulatory evaluationWenlei Jiang, Stephanie Kim, Xinyuan Zhang, et al.Current Opinion in Microbiology|June 9, 2005
Bridging the imaging gap: visualizing subcellular architecture with electron tomographySriram SubramaniamBiophysical Reviews|December 5, 2022
Learning from Gobind Khorana: "The difficult we do today, the impossible tomorrow"Sriram SubramaniamPageof 21