Do you require help with the registration and approval of pharmaceuticals or medical products in Europe?
We are here to offer our support.
As a Drug Regulatory Affairs service provider with a high level of technical and cross-cultural expertise, Menapharm Deutschland GmbH will help you master the regional and country-specific aspects of the regulatory processes in both regions.
Our services at a glance:
Support in the registration and approval process:
Compilation of the required documents and documentation in CTD/eCTD format.
For further information, please contact us here.