Post-market Surveillance and Vigilance under the Medical Device Regulation (MDR) and In Vitro Diagnostics Medical Devices Regulation (IVDR) Training Course

Level Specialist Duration 4 hours

Available to book: On-demand elearning Book your place

This intensive course enables manufacturers to learn about the key requirements, concepts and the overall process for post-market surveillance and vigilance under the MDR and IVDR.

BSI’s on-demand courses are market-leading and available 24/7. Developed by top subject matter experts, they contain the same high-quality content you will find in our tutor-led training, but with the added benefit of being able to learn at your own pace and at any time.

How will I benefit?

The course will help you:

Understand the key requirements and concepts of the post-market surveillance and vigilance for the MDR and IVDR
Gain sufficient understanding to be able to write your PMS and vigilance procedures
Communicate the impact of these key requirements introduced by the MDR and IVDR to your organization
To obtain essential knowledge to implement a compliant post-market surveillance and vigilance quality management system
To understand how the PMS and vigil

On completion of this training, you’ll be able to:
- Interpret regulatory requirements for post-market surveillance and vigilance under the MDR and IVDR
- Identify how these requirements relate to ISO 13485:2016, ISO 14971:2019 and various European and IMDRF (GHTF) guidance documents
- Create a post-market surveillance plan that includes both proactive and reactive sources of information
- Implement appropriate post-market clinical follow-up (PMCF) and post-market performance follow-up (PMPF) as per the MDR and IVDR respectively
- Recognize when incidents and adverse event need to be reported to the Competent Authorities and Notified Bodies for both pre and post CE marked devices
This course is ideal for you if you’re in a quality assurance/quality control/regulatory/patient safety/customer facing role involved in continuous improvement and customer advocacy.
You should have a basic understanding of European Medical Device and In-vitro Diagnostic Regulations (MDR).

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