Post Market Surveillance and Vigilance

Post Market Surveillance & Vigilance: New Requirements under the EUMDR/IVDR; 1-Day Session; Virtual Training; November 10, 2026

Schedule (all times EST)

9:00am - 5:00pm

About the Training

Both Regulation (EU) 2017/745 (MDR) and (EU) 2017/746 (IVDR) include new and more detailed Post-market surveillance and vigilance requirements.

The transitional provisions described in both Regulations (MDR Article 120, IVDR Article 110), require a manufacturer to implement the Post-market surveillance, market surveillance, vigilance requirements during the transitional period in order to keep placing its Device on the market with a Medical Device Directive certificate after the date of the Regulations application. For the Regulation (EU) 2017/745, it is starting May 27, 2021; for the Regulation (EU) 2017/746, May 27, 2022.

This course has been designed to allow manufacturers to easily identify the key requirements and prepare for their timely implementation.

For program and more information, click here.