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INTRODUCING PRODUCT -SPECIFIC BIOEQUIVALENCE GUIDELINES IN CUBA

  • At: 2015 FIP Congress in Düsseldorf (Germany)
  • Type: Poster
  • By: SUáREZ PéREZ, Yamira (Centre for State Quality Control of Drugs Equipment and Medical Devices (CECMED), Department of Assessment and Research of Medicinal Products, Havana, Cuba)
  • Co-author(s): Yamira Suárez Pérez
  • Abstract:

    Regulatory framework for demonstration of bioequivalence(BE) in Cuba is set and improving.



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Last update 4 October 2019

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