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
.. The access to the whole abstract and if available the presentation file is available to FIP members and to congress participants of that specific congress.
Please login
Last update 28 September 2023