Webinar: Post-Marketing Activities under the Medical Device Regulation
Due to the medical nature of the devices, incidents are bound to happen sooner or later. It is therefore crucial for any manufacturer to know how to react!
Did you know? It is a legal obligation to report incidents to the Competent Authorities and to maintain a Medical Devices Post Market Surveillance System!
In this webinar we provide an overview on:
- QMS obligations by the MDR
- Market Surveillance
- Post Market Surveillance: Vigilance, Field Safety Corrective Action
- Economic Operator’s PMS duties
- Obelis PMS services