The CE mark is your medical device product’s passport to the EU and certifies its adherence to health, safety and environmental requirements and translations are the keys to successful compliance.
With greater importance being placed on the translation of documentation to ascertain the coveted CE mark for your medical device’s successful release in the EU and member countries, more medical device manufacturers find themselves in an endless loop of questions and concerns.
You may be asking yourself about what languages are required for translation or what materials need to be translated. So we have created a brand new guide to support your medical device release, in our “CE Mark Translation: Your Passport to the EU” Guide answer your questions to:
Download our “CE Mark Translation: Your Passport to the EU” today to learn the translation requirements for CE marking and how Morningside can support your next product launch. Receive your complimentary copy of this guide by completing the form below.