EEU Common Drug Market: The Time Has Come!
For appropriate functioning of the EEU Common Drug Market, 67 regulatory “medicinal” documents will have to be approved. The list and status of these drugs will have to be approved by a specialized work group of EEC.
Two projects requiring urgent review and approval have already been adopted, including Good Practice of Cultivation, Growing and Collection of Herbal Raw Materials and Guidelines for Validation of Analytical Methods.
A pilot project for authorization of a few drugs at the common EEU market was suggested. If implemented, it will help work out the procedure of expert assessment and interaction of expert panels of EEU member states.