Driving ‘A safer healthcare ecosystem’

The European Union Medical Device Regulation (EU MDR) brings a wider and clearer regulatory scope which enforces stricter requirements on manufacturers and notified bodies. 

Request your free copy and learn

• The important dates of application
• How the MDR will affect medical device R&D and market access
• How the MDR will impact current and future CE marks
• Why clinical evidence and data is of utmost importance