MDR solution brief
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The EU’s Medical Device Regulation (MDR) has presented new challenges for medical device manufacturers, requiring them to supply documentation in multiple languages for products marketed in the EU. 

At RWS, we offer a proven and trusted solution underpinned by our linguistic skill, deep understanding of the industry, and highly specialized regulatory knowledge. Our comprehensive services have been carefully designed to provide you with greater content control and oversight, ensuring global compliance in all your target markets. 

Download our solution brief to learn more about how we can support you with MDR compliance.


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