Research & Business Park

Approvals

In Denmark it is simpler and faster than anywhere else in Europe to apply for clinical trial authorization, for instance:

  • Danish Medicines Agency applications are handled within 30 days. Applications can be submitted in English.
     
  • The local Ethics Committee meets once a month (once a month). Applications can be submitted in English with a Danish summary.
     
  • The regulatory environment in Denmark is highly developed and the regulatory authorities are helpful with advice as how to approach EMA (European Medicine Agency) for specific development programs.



 

 

 




 

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