Webinar
Medical Devices

The Periodic Safety Update Report (PSUR) & Vigilance under the MDR

This webinar will focus on medical devices with ancillary medicinal substance and the conformity assessment process and key requirements.

Watch the Webinar View the Presentation

In this webinar:

Relevant information you need to know about for the Periodic Safety Update Report.
What information should be presented and how it should be presented.
Understand what types of events are reportable under the Medical Device Regulations (MDR).
Better understanding of the post market requirements as listed under Articles 86 and 87 of the MDR.

The Periodic Safety Update Report (PSUR) & Vigilance under the MDR

Information you need to know about for the Periodic Safety Update Report, what information should be presented and how it should be presented.

Richard Holborow, Head of Clinical Compliance, BSI

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