
How to Prepare IFU Translations for an MDR Audit
Under the EU Medical Device Regulation, the Instructions for Use (IFU) are no longer just supporting documentation—they are a core part of the safety information
We support global pharmaceutical companies looking to launch drugs in overseas markets with our translation and localization services.
Developing new drugs is a lengthy process that costs pharmaceutical companies millions of euros in investment. It can take as much as 10 years from the beginning of the research phase until the market launch.
More than 50% of the
investment spending
is allocated to the design, development, and evaluation of phases 1, 2, and 3 of clinical trials.
Only 1 in 5 drugs
that reach the market is able to generate revenues that exceed the overall R&D costs.
We facilitate the onboarding and professional development of your sales team by translating and adapting your training materials to each local market.
We’ve been supporting marketing departments in pharmaceutical companies with new product launches for +15 years.
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How to Prepare IFU Translations for an MDR Audit
Under the EU Medical Device Regulation, the Instructions for Use (IFU) are no longer just supporting documentation—they are a core part of the safety information