Drug registration and other services

Do you require help with the registration and approval of pharmaceuticals or medical products in 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.


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