Session Medical Devices (online)

Thursday, December 3, 2020 from 2:00 PM to 4:00 PM Regulatory Affairs

Agenda

14:00 - 14:05 Welcome and introduction Annabelle Bruyndonckx
Healixia
14:05 - 14:30 State of play on MDR and IVDR implementation Valérie Nys
Program Manager - FAMHP
14:30 - 14:55 Medical Devices Regulations: Should the pharma industry be concerned? Vladimir Murovec
Simmons & Simmons
14:55 - 15:05 Q&A All speakers
15:05 - 15:30 Lessons learned from the first MDR and IVDR projects  Julien Senac
TÜV SÜD
15:30 - 15:50 Evaluation old pact and elements new pact: Industry perspective Marnix Denys 
beMedtech
15:50 - 16:00 Q&A All speakers
16:00 Thank you & closing comments Elke Debie
Healixia

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