Marketing Authorisation Applications for new products, as well as variations. Strategic support early in the process when translation is needed.

Medical Device and combination product expertise

Evolving Pressure

Project management burden of dealing with LSPs and design agencies
Affiliate/in-country review

MDR is here:

Must comply with the new regulations.
Many products being up-classified, increased volume of clinical and safety data required.
Summary of Safety and Clinical Performance for high-risk devices.

ISO 9001 + roadmap towards 13485.​

Marketing + transcreation/localization (Something here from Matthew’s team)




In-house medical expertise + typical translator profile


Blog post: who translates your medical texts?

Languages covered – we cover your top-selling countries, and we know how to prepare them for printing…



Language Vault


Unification: eLearning / Interps / Marketing / Clinical / Patents / Desktop Publishing

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