22 - 24 October, 2019 | Mercure Hotel MOA Berlin, Berlin, Germany
Milena Roux, Regulatory Professional at Novo Nordisk
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Milena Roux

Regulatory Professional
Novo Nordisk

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

Download The Latest Agenda

Main Conference Day One

Wednesday, October 23rd, 2019

2:50 PM Roundtable Discussions:

Use this opportunity to benchmark with your peers and identify the key strategies required to optimise your lifecycle management process, from concept to market. Use this 40 min opportunity to discuss your chosen topic and benchmark with your peers.
  • Lifecycle management and registering products across the globe
  • How to structure the regulatory submission 
  • Challenges to the implementation of Article 117 under the MDR

Main Conference Day Two

Thursday, October 24th, 2019

9:50 AM Lifecycle Management And Registering Products Across The Globe

  • Understand the regulatory requirements for your combination product as a whole
  • Review the transition between the medical device directive and the upcoming EU MDR
  • Learn how regulations differ across the globe and how you can alter your strategy to adapt to this
  • Discover how the registration process differs in China with case study insights