“Over the past few months, we’ve been working at full pace to ensure that our products and services meet the requirements of the MDR. With the MDR Suite, we’re taking this a step further and providing orthopaedics businesses with a tool that lets them focus their full attention on treating their patients.”
Dr Thomas Meininghaus, Vice President Global Regulatory Affairs at Ottobock
Learn more about
- The requirements of the EU Medical Device Regulation
- The features of the new MDR Suite
- The advantages the MDR Suite offers for orthopaedics businesses
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