Pharma Registrations – licences et enregistrements

IVDR, ISO13485, FDA, WHO, NAT controls, NatTrols, TrueNAT, EasyNAT


Inward and outward licensing of pharmaceuticals and technologies is an essential part of PharmaRegistrations’ activities. Our development effort, focussed on value added and low-cost drugs and technologies, results in a portfolio of generics, first-to-market generics, value-added OTC and generic formulations.

Acquisition of complementary pharmaceuticals and technologies, results in a complete portfolio of readily available marketing authorizations, registration dossiers and development projects.

We have an in-house team of 2 licensing managers + our representatives in foreign countries at your service for your personal licensing needs.

Additional services will complement your business development activities: market research and taylor-made development projects.

At your request: involvement in your EU-registration process. We conclude registration dossiers for new products and line-extensions in order to obtain European approvals. See also regulatory affairs.