Language Requirements Under the EU MDR

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