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International regulatory issues for innovative medicines

  • At: 2006 FIP Congress in Salvadore (Brazil)
  • Type: Presentation
  • By: JUILLET, Yves (Leem, General Management, Paris Cedex 16, France)
  • Abstract:

    The aim of harmonisation of regulatory requirements for registration is to allow patients quicker access to new drugs , to avoid animal and human trials duplication but also guaranteeing at the same time public health and patient safety. Harmonisation of regulation in the European Union (EU) is now completed, and has led to the submission

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Last update 4 October 2019

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