Drug registration and other services

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



For further information, please contact us here.

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1 Gilt für Lieferungen in folgendes Land: Deutschland. Lieferzeiten für andere Länder und Informationen zur Berechnung des Liefertermins siehe hier: Liefer- und Zahlungsbedingungen