About This Webinar
This training aims at providing a comprehensive overview of the regulatory system and requirements for medical devices in Europe with particular focus on combination products.
  • Highlight of the key changes in the MDR 2017/745 Update latest changes
  • MDR Implementation for Medical Devices – Industry Perspective
  • MDR Implementation for Article 117 impacted combination products – Industry Perspective
  • 1598611000-fe4ba86200f3b0e9
    Karin Schulze
    Head of Medical Devices, SFL
  • 1598611127-e41c99c1b8a8f8b4
    Stephan Affolter
    Regulatory and Quality Intelligence Manager, Ypsomed
  • 1598615640-fbb7562cfbaa2094
    Juan Martin Carriquiry
    EU MDR Expert, Device Development & Commercialization, Novartis