EU Language Requirements : Medical Devices/IVDs



Hi all,

Just wondering if anyone has a comprehensive resource that outlines the language/translation requirements of the different EU member states?

I've found some great resources on the internet, but these are mostly out dated and im struggling to find something recent.

This is in relation to Medical Devices/IVDs and their outer box/IFU/Software language requirements...

Thanks in advance :)


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I'm not aware of anything truly up to date, even then I probably wouldn't trust it as some of the rules/exceptions can be very specific and summaries tend to miss them. Your best bet is to look on the website of each competent authority
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