Webinar: Overview of Medical Devices Regulation and Impacts on Combination Products by Level-up Events

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WEBINAR ENDED

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.

Agenda

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

Presenters

Karin Schulze

Head of Medical Devices, SFL

Stephan Affolter

Regulatory and Quality Intelligence Manager, Ypsomed

Juan Martin Carriquiry

EU MDR Expert, Device Development & Commercialization, Novartis

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