Overview of Requirement Related to Article 120(3) of MDR 2017/745

In this webinar, representatives from Intertek's Medical Notified Body address requirements as presented by Article 120 (3) of the Medical Device Regulation 2017/745. This webinar is roughly 45 minutes long and covers:

  • A background of the MDR 2017/745 and art. 120 (3)
  • Transitional provisions
  • Changes affected under MDD due to 2017/745 art. 120 (3)
  • Significant changes
  • Post market surveillance
  • Registration of devices
  • Registration of economic operators
  • Key points to consider
  • Helpful references

To view the webinar, please fill out the form below.