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Responsibility for authorities and payers

  • In: D2 - Sustainable flow of pharmaceuticals on Saturday, 5 September 2009, 14:00-17:00
  • At: Istanbul (Turkey) (2009)
  • Type: Presentation
  • By: RECHENBERG, Bettina (German Federal Environmental Agency Umweltbundesamt, Dessau, Germany)
  • Abstract:

    European legislation requires an environmental risk assessment within the pharmaceutical authorization procedure. Authorisation of a human medicinal product, however, can explicitly not be denied if an environmental risk is identified. For veterinary pharmaceuticals the legal situation is different - authorisation may be denied, or may be limited


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Last update 28 September 2023

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