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Language Requirements Under the EU MDR

When and what to translate after the Date of Application

Communication and Compliance

After a delay due to the COVID-19 pandemic, the EU MDR is now in effect. For over a year, our team has been keeping you up-to-date with how this regulation can impact your work in medical devices. 

We've talked about clinical outcome assessments, patient literacy, post-market surveillance and more. Our capstone piece is a whitepaper on language and regulation harmonization in the EU. Download the piece below to learn:

  • Where in the lifecycle translations are needed
  • How different levels of governance will impact you
  • When each change towards compliance must be completed
  • #regulated_translation_localization
  • #life_sciences

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