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2. Update to the PhRMA perspective on population and individual bioequivalence. Barrett JS; Batra V; Chow A; Cook J; Gould AL; Heller AH; Lo MW; Patterson SD; Smith BP; Stritar JA; Vega JM; Zariffa N J Clin Pharmacol; 2000 Jun; 40(6):571-2. PubMed ID: 10868306 [No Abstract] [Full Text] [Related]
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4. The U.S. draft guidance regarding population and individual bioequivalence approaches: comments by a research-based pharmaceutical company. Hauschke D; Steinijans VW Stat Med; 2000 Oct; 19(20):2769-74. PubMed ID: 11033574 [TBL] [Abstract][Full Text] [Related]
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9. Mean difference vs. variability reduction: tradeoffs in aggregate measures for individual bioequivalence. FDA Individual Bioequivalence Working Group. Hauck WW; Chen ML; Hyslop T; Patnaik R; Schuirmann D; Williams R Int J Clin Pharmacol Ther; 1996 Dec; 34(12):535-41. PubMed ID: 8996848 [TBL] [Abstract][Full Text] [Related]
10. Subject-by-formulation interaction in bioequivalence: conceptual and statistical issues. FDA Population/Individual Bioequivalence Working Group. Food and Drug Administration. Hauck WW; Hyslop T; Chen ML; Patnaik R; Williams RL Pharm Res; 2000 Apr; 17(4):375-80. PubMed ID: 10870978 [TBL] [Abstract][Full Text] [Related]
11. Drug bioequivalence. Recommendations from the Drug Bioequivalence Study Panel to the Office of Technology Assessment, Congress of the United States. J Pharmacokinet Biopharm; 1974 Oct; 2(5):433-66. PubMed ID: 4452945 [No Abstract] [Full Text] [Related]
12. Generic drugs and the elderly. Lasagna L J Am Geriatr Soc; 1983 Sep; 31(9):571-2. PubMed ID: 6886286 [No Abstract] [Full Text] [Related]
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