EU Medical Device Regulation | MedTech: EU MDR Exchange

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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

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Benchmark With The Latest EU MDR Experiences, Developments And Strategies

Interactive And Easily Digestible Formats Including:

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
Interview with Richard Houlihan, CEO, EUDAMED, sharing experiences and updates on EUDAMED

Industry Case Studies, Key Learnings And Advice

Industry Case Studies, Key Learnings And Advice

Cook Medical outline the resources taken to obtain and keep an EU MDR CE Mark to avoid key submission challenges
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:

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