On-Demand Webinar
On-Demand Webinar
Join medical device experts from TÜV SÜD, Materialise and AKRA Team as they discuss the differences in MDR regulatory pathway for custom made and patient matched medical devices.
Duration: 80 minutes
We will kickstart with a 40-minute presentation, covering the following points:
After the presentation, viewers will engage in a 40-minute panel discussion with the speakers, moderated by Dr Andrea Pietsch.
Dr Andrea Pietsch (Moderator)
TÜV SÜD Product Service MHS Director Global Focus Team Orthopedics
Jeff Bennett
TÜV SÜD Product Service MHS, Orthopedic Expert & Product Specialist
Matthias Fink
AKRA Team GmbH, Senior Clinical Consultant
Jenny Jones
Materialise, Global Quality Regulatory Manager
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