Webinar 6:

Re-certification

Part 6 (of 6) of the webinar series "The New EU Medical Device Regulation".
Date: 13.09.2018
Time: 16.00 - 17.00 CET
AGENDA
Topics covered
  • Notified Bodies under the New MDR
  • Effect on NBs
  • When will NBs begin conformity assessment against the new Regulation?
  • Main effect on medical device manufacturers
  • Recertifications
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