Post Market Surveillance and Vigilance

Post Market Surveillance and Vigilance

0 followers166 events14y hosting439 total attendees
Online event
Tuesday, November 10  •  9 AM - 5 PM EST
Overview

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.

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.

Good to know

Highlights

  • 8 hours
  • Online

Refund Policy

Refunds up to 14 days before event

Location

Online event

Organized by
GMED North America, Inc.
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Events166
Hosting14 years
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