Webinar 4:

Clinical testing

Part 4 (of 6) of the webinar series "The New EU Medical Device Regulation".
Date: 30.08.2018
Time: 16.00 - 17.00 CET
AGENDA
Topics covered
  • Class I and IIa devices
  • Effect on class IIb devices
  • Class III devices
WHO
should attend
  • Clinical Trial Managers
  • Regulatory Affairs Professionals
  • Medical Officers
WHY
you should
attend
  • Because the current directive will be significantly altered
  • ...and replaced by a regulation which is legally binding on all EU member states.
Book this webinar:
Single attendee: € 150 Book online in our webshop
Corporate groups:
(more than one and up to a group of 10 participants from your company)
€ 290 Book online in our webshop

...or contact us for further information and other booking options:

Phone: +43 (0)1 890 57 14, E-mail: office@michor-consulting.eu

Would you like to book the whole series of 6 webinars?

This webinar is part of the webinar series "The New EU Medical Device Regulation".
Overview of the whole series