Evaluation of the effects of different sampling schedules on the assessment of bioequivalence

• In: SIG: Bioavailability/Bioequivalence - Posters
• At: Basel (Switzerland) (2008)
• Type: Poster
• Poster code: BB-P-018
• By: PORTA, Valentina (College of Pharmaceutical Sciences, University of São Paulo, SÃo Paulo, Brazil)
• Co-author(s): Kano, Eunice Kazue (College of Pharmaceutical Sciences, University of São Paulo, SÃO PAULO, Brazil)
  Fukuda, Kazuo (College of Pharmaceutical Sciences, University of São Paulo, SÃO PAULO, Brazil)
  Chiann, Chang (Institute of Mathematics and Statistics, University of São Paulo, Brazil)
  
• Abstract:

  Bioequivalence studies are designed to compare the in vivo performance of different pharmaceutical products. The most frequently used pharmacokinetic parameters to evaluate bioequivalence are area under the plasma concentration-time curve (AUC), maximum plasmatic concentration (Cmax) and time to achieve Cmax (Tmax). Accuracy in measuring..

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