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.

• Preparation of registration dossiers
• Submission of the registration application on your behalf
• Communication with the local authorities
• Acquisition of suitable distribution partners
• Support in establishing local subsidiaries
• Establishing legal and organisational platforms

Questions?

For further information, please contact us here.