In Article 49 of Directive 2001/83 (for veterinary medicinal products, please read Article 53 of Directive 2001/82) – please see the QP Regulations, the qualification level as well as the necessary professional experience of a QP is defined. The EU requirements as defined in these Directives have to be transferred to national law in each EU Member State. However, there are a number of differences in the EU Member States due to the fact that each Member State can implement the directives into national law with slight modifications.
Our recommendation is to discuss this matter with the respective authority in the Member State you plan to work as QP.
