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17篇 您的检索式:作者名="Conner DP"
    题名 作者 年代 出处 被引量
1Implementation of a reference-scaled average bioequivalence approach for highly vari- able generic drug products by the US Food and Drug Administra- tion显示文摘DAVIT BM CHEN ML CONNER DP 2012AAPS J2012,14,4:1
2Use of reflectance spectrophotometry in the human corticosteroid skin blanching assay显示文摘 Zamani K Alminez RG 1993J Clin Pharmacol1993,33,8:1
3Highly variable drugs: observations from bioequivalence data submitted to the FDA for new generic drug applications 显示文摘Davit BM Conner DP Fabian-Fritsch B 2008AAPS J2008,10,1:1
4Implementation of a reference-scaled average bioequivalence approach for highly variable generic drug products by the US Food and Drug Administration 显示文摘Davit BM Chen ML Conner DP 2012AAPS J2012,14,4:1
5Effect of food on the absorption of enteric-coated asprin:correlation with gastric residence time显示文摘Mojaverian P Rocci ML Conner DP 1987Clin Pharmacol Ther1987,41,:1
6International guidelines for bioequivalenee of systemically available orally administered generic drug products: a survey of similarities and differences 显示文摘Davit B1 Braddy AC Conner DP 2013AAPS J2013,15,4:1
7Implementation of a reference-scaled average bioequivalence approach for highly varia- ble generic drug products by the US Food and Drug Administra- tion显示文摘DAVIT BM CHEN ML CONNER DP 2012AAPS J2012,14,4:1
8Implementation of a reference-scaled average bioequivalence approach for highly vari- able generic drug products by the US Food and Drug Administra- tion显示文摘DAVIT BM CHEN ML CONNER DP 2012AAPS J2012,14,4:1
9Dissolution testing forgeneric drugs : an FDA perspective 显示文摘ANAND 0 YU LX CONNER DP 2011AAPS2011,13,3:1
10Removal of dislocated intraocular lenses using pars、plana vitrectomy with placement of an openloop,flexible anterior chamber lens显示文摘Mittra RA Conner TB Han Dp 1999Ophthalmology1999,17,:1
11Dissolution testing forgeneric drugs : an FDA perspective 显示文摘ANAND 0 YU LX CONNER DP 2011AAPS2011,13,3:1
12Highly varia- ble drugs:observations from bioequivalence data submitted to the FDA for new generic drug applications 显示文摘DAVIT BM CONNER DP FABIAN-FRITSCH B 2008J2008,10,1:1
13Highly variable drugs: observations from bioequivalence data submitted to the FDA for new generic drug applications 显示文摘DAVIT BM CONNER DP FABIAN-FR1TSCH B 2008AAPS J2008,10,1:1
14Implementation of a reference-scaled average bioequivalence approach for highly var- iable generic drug products by the US Food and Drug Administra- tion显示文摘DAVIT BM CHEN ML CONNER DP 2012AAPS J2012,14,4:1
15Influence of drug release properties of conventional solid dosage forms on the systemic exposure of highly soluble drugs显示文摘Yu LX Ellison CD Conner DP 2001AAPSPharm Sci2001,3,3:1
16Implementation of a reference-scaled average bioequivalence approach for highly var- iable generic drug products by the US Food and Drug Administra- tion显示文摘DAVIT BM CHEN ML CONNER DP 2012AAPS J2012,14,4:1
17International guide- lines for bioequivalence of systemically available orally adminis- tered generic drug products: a survey of similarities and differ- ences显示文摘DAVIT B BRADDY AC CONNER DP 2013AAPS J2013,15,4:1
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