24 - 25 April, 2019 | Brussels, Belgium

Céline Bourguignon

Director Global Regulatory Policy
Johnson & Johnson

9:50 AM Translating The MDR – What We Know So Far

- Current shift in global focus – from FDA to European MDR
- Discuss an implementation timeline of regulatory changes for new device developments, ongoing device developments and legacy devices
- Understand the requirements – what can you be doing now to move beyond tick box regulatory compliance for your UDI implementation

Check out the incredible speaker line-up to see who will be joining Céline.

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