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3. Summary report of second EUFEPS/AAPS conference on global harmonization in bioequivalence. Chen ML; Blume H; Beuerle G; Mehta M; Potthast H; Brandt A; Schug BS; Ducharme M; Endrenyi L; Gallicano K; Schuirmann D; Welink J Eur J Pharm Sci; 2019 Jan; 127():24-28. PubMed ID: 30342171 [TBL] [Abstract][Full Text] [Related]
4. The Global Bioequivalence Harmonization Initiative: Summary report for EUFEPS international conference. Chen ML; Blume H; Beuerle G; Davit B; Mehta M; Potthast H; Schug B; Tsang YC; Wedemeyer RS; Weitschies W; Welink J Eur J Pharm Sci; 2018 Jan; 111():153-157. PubMed ID: 28964950 [TBL] [Abstract][Full Text] [Related]
5. The global bioequivalence harmonisation initiative: Report of EUFEPS/AAPS third conference. Mehta M; Blume H; Beuerle G; Tampal N; Schug B; Potthast H; Jiang W; Wilson C Eur J Pharm Sci; 2020 Aug; 151():105383. PubMed ID: 32473200 [TBL] [Abstract][Full Text] [Related]
6. Considerations for metabolite pharmacokinetic data in bioavailability/bioequivalence assessments. Overview of the recent trends. Srinivas NR Arzneimittelforschung; 2009; 59(4):155-65. PubMed ID: 19517891 [TBL] [Abstract][Full Text] [Related]
7. The 2nd Calibration and Validation Group workshop on recent issues in good laboratory practice bioanalysis. Savoie N; Booth BP; Bradley T; Garofolo F; Hughes NC; Hussain S; King SP; Lindsay M; Lowes S; Ormsby E; Phull R; Rocci ML; Vallano PT; Viau A; Zhu Z Bioanalysis; 2009 Apr; 1(1):19-30. PubMed ID: 21083184 [TBL] [Abstract][Full Text] [Related]
8. BIO-international '94 Conference on Bioavailability, Bioequivalence and Pharmacokinetic Studies and Pre-Conference Satellite on 'In Vivo/In Vitro Correlation'. Munich, Germany, June 14-17, 1994. Blume HH; McGilveray IJ; Midha KK Eur J Drug Metab Pharmacokinet; 1995; 20(1):3-13. PubMed ID: 7588991 [No Abstract] [Full Text] [Related]
10. Metabolites and bioequivalence: past and present. Jackson AJ; Robbie G; Marroum P Clin Pharmacokinet; 2004; 43(10):655-72. PubMed ID: 15244496 [TBL] [Abstract][Full Text] [Related]
11. When are bioavailability studies required? A German proposal. Gleiter CH; Klotz U; Kuhlmann J; Blume H; Stanislaus F; Harder S; Paulus H; Poethko-Müller C; Holz-Slomczyk M J Clin Pharmacol; 1998 Oct; 38(10):904-11. PubMed ID: 9807970 [TBL] [Abstract][Full Text] [Related]
13. Bioavailability and Bioequivalence Aspects of Oral Modified-Release Drug Products. Wang R; Conner DP; Li BV AAPS J; 2017 Mar; 19(2):360-366. PubMed ID: 28004346 [TBL] [Abstract][Full Text] [Related]
14. [Bioavailability of drug products and bioequivalence requirements (author's transl)]. Jaminet F J Pharm Belg; 1978; 33(3):141-56. PubMed ID: 682101 [No Abstract] [Full Text] [Related]
15. Regulated drug bioanalysis for human pharmacokinetic studies and therapeutic drug management. Huang Y; Shi R; Gee W; Bonderud R Bioanalysis; 2012 Aug; 4(15):1919-31. PubMed ID: 22943622 [TBL] [Abstract][Full Text] [Related]
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17. The bioequivalence of highly variable drugs and drug products. Midha KK; Rawson MJ; Hubbard JW Int J Clin Pharmacol Ther; 2005 Oct; 43(10):485-98. PubMed ID: 16240706 [TBL] [Abstract][Full Text] [Related]
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