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Application of simultaneous dissolution-absorption apparatus for screening formulations before bioequivalence studies

  • At: 2017 FIP Congress in Stockholm (Sweden)
  • Type: Poster
  • By: BORBáS, Enikő (Budapest University of Technology and Economics, Organic Chemistry and Technology, Budapest, Hungary)
  • Co-author(s): Bálint Sinkó: Pion Inc., Billerica, MA, United States
    Enikő Borbás: Organic Chemistry and Technology, Budapest University of Technology and Economics, Budapest, Hungary
    Zsombor Kristóf Nagy: Organic Chemistry and Technology, Budapest University of Technology and Economics, Budapest, Hungary
    Konstantin Tsinman: Pion Inc., Billerica, MA, United States
  • Abstract:

    Backgrounds

    For generic drug development traditional dissolution tests have been used in the pharmaceutical industry to compare performance of different drug product formulations before conducting bioequivalence studies, even though the in vivo predictive power of these tests are questionable. Namely, when a poorly water-soluble API is formulated

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Last update 4 October 2019

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