EU Medical Device Regulation | MedTech: EU MDR Exchange

This site is part of the Informa Connect Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 3099067.

Accelerate Your EU MDR Strategy To World Class Levels

Streamline Processes. Optimise Resources. Maintain Market Access

Through Practical Insights And Knowledge Exchange With Leading Medical Device Professionals, Notified Bodies and the EU Commission

See the full agenda Book Now

Benchmark With The Latest EU MDR Experiences, Developments And Strategies

Interactive And Easily Digestible Formats Including:

Dual Dialogues with Notified Body and Industry on first learnings with TÜV SÜD and BD
Multi-speaker case studies on first experiences on the MDR with feedback from Stryker and Advanced Bionics
Update with Richard Houlihan, CEO, EUDAMED, sharing experiences and updates on EUDAMED

Industry Case Studies, Key Learnings And Advice

Get best practices to balance MDD and EU MDR products
Marianna Luppi, Regulatory and Clinical Affairs Expert, shares first experiences with bringing a new device to market under the EU MDR and advance your processes
Valoc share practical advice on the identification and evaluation of risks

Join Roundtable Discussions For Multiple Perspectives On:

First Experiences of Economic Operators under the EU MDR with Vanessa Windscheid, RAQA Director, Nipro-Group
Requirements of Annex 16 under the EU MDR with Dr Melania Battistella, Global Manager Aesthetic Products, TÜV SÜD