Client
Manufacturer of medical devices, based in France
The client’s concern
Speed
The client’s brief
The EU Medical Device Regulation had been approved in 2017 and needed to be implemented by May 2021. Our client operates in all European countries and faced the challenge of arranging the translation of all its technical documentation into the 22 common languages of the European Union. Due to various organisational and technical reasons, the updated documentation materials (a total of several hundred pages) only became available for translation one month before the deadline.
Lexitech’s solution
Fast response time
Thanks to Lexitech’s extensive and well-developed network of translators, Lexitech was able to deliver all translations of the documentation materials on time and within the set budget. What was the result? Business as usual for the client, everywhere in Europe, just as before. And all of the client’s documentation fully compliant with the Medical Device Regulation.
What problem did Lexitech resolve?
The client’s business outside its home country was at risk because its legal documentation was not available in the 22 common EU languages.