The webinar will inform you about the principles of vigilance reporting under UK CA and EU CE marking in the UK. In addition, we will dive deeper into the new MORE portal; relevant timelines, registration and maintenance of user accounts, its coherence with the MHRA device registration database, and the documents that are involved in the vigilance reporting process.
The webinar discussed the following topics:
- Adverse events
- Post-market surveillance
- MORE portal
- UKCA
Watch the webinar On-Demand or download the corresponding presentation.