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Switchability of drug products: scientists vs. lawmakers

  • In: Moving forward drug product Quality (SIG Bioavailability/Bioequivalence) on Tuesday, 7 September 2004, 9:00-12:00
  • At: New Orleans (USA) (2004)
  • Type: Presentation
  • By: DRESSMAN, Jennifer (Institute of Pharmaceutical Technology, J.W. Goethe University, Frankfurt Am Main, Germany)
  • Abstract:

    For many years now, regulations have been in place setting out the requirements for generic substitution of drug products. Important requirements include pharmaceutical equivalence, bioequivalence and therapeutic equivalence of the generic product with the reference product. While various authorities differ slightly in their definitions of


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Last update 28 September 2023

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