EU Medical Device Regulation and Languages Q&A


Download our whitepaper to find the answers for questions we frequently asked by life sciences companies such as:

  • How do the regulations differ for devices that are intended for use by patients vs medical professionals?

  • What additional content must be translated as a result of the MDR changes?

  • Are there any restrictions to what type of symbols we can use?

If you want to learn more about the areas that will be affected once the new Medical Device Regulation comes into effect, check here

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