Available for 90 days after enrollment
E-learning content is available on demand!
This webinar will provide you with the relevant information you need to know about for the Periodic Safety Update Report, including what information should be presented and how it should be presented. The webinar will also help you to understand what types of events are reportable under the Medical Device Regulations (MDR).
Who should attend the webinar?
This webinar will offer notified body insights for all people involved in working towards an MDR application and will be of particular interest to those individuals who are involved in post market surveillance activities for their organization.