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The AAPS Journal|April 2, 2013
Sequential bioequivalence trial designs with increased power and controlled type I error ratesAnders FuglsangThe AAPS Journal|May 21, 2013
Bioequivalence for locally acting nasal spray and nasal aerosol products: standard development and generic approvalBing V Li, Feiyan Jin, Sau L Lee, et al.The AAPS Journal|December 18, 2012
The twofold advantage of the amorphous form as an oral drug delivery practice for lipophilic compounds: increased apparent solubility and drug flux through the intestinal membraneArik Dahan, Avital Beig, Viktoriya Ioffe-Dahan, et al.The AAPS Journal|January 25, 2013
A sensitivity analysis of the modified chi-square ratio statistic for equivalence testing of aerodynamic particle size distributionBenjamin Weber, Sau L Lee, Robert Lionberger, et al.The AAPS Journal|January 16, 2013
Strategic applications of gene expression: from drug discovery/development to bedsideJane P F Bai, Alexander V Alekseyenko, Alexander Statnikov, et al.The AAPS Journal|February 8, 2013
Nonaqueous gel for the transdermal delivery of a DTPA penta-ethyl ester prodrugYong Zhang, Matthew P Sadgrove, Katsuhiko Sueda, et al.The AAPS Journal|February 9, 2013
Predictions of in vivo prolactin levels from in vitro K(i) values of D(2) receptor antagonists using an agonist-antagonist interaction modelKlas J Petersson, An M Vermeulen, Lena E FribergThe AAPS Journal|January 29, 2013
Simultaneous pharmacokinetic model for rolofylline and both M1-trans and M1-cis metabolitesMark Stroh, Matthew M Hutmacher, Jianmei Pang, et al.The AAPS Journal|January 12, 2013
Improper selection of a pre-specified primary dose-response analysis delays regulatory drug approvalJiang Liu, Pravin Jadhav, Yaning Wang, et al.The AAPS Journal|December 28, 2012
Dose selection based on physiologically based pharmacokinetic (PBPK) approachesHannah M Jones, Kapil Mayawala, Patrick PoulinPageof 235