Co-ordinating bodies

  • Email
  • Help

In this section you will find information on the groups set up as per the revised pharmaceutical legislation (Directive 2004/27/EC amending Directive 2001/83/EC) for the examination of any question relating to marketing authorisation of a medicinal product in two or more Member States in accordance with the mutual recognition procedure or the decentralised procedure.

How helpful is this page?

Average rating:

 Based on 10 ratings

Add your rating:

See all ratings
9 ratings
0 ratings
0 ratings
1 ratings
0 ratings
    

Tell us more