Webinar – Materiovigilance – All you need to know about the new European regulation on Medical Devices (RUE 2017/745)
Universal Medica pleased to announce its next webinar on Friday 23rd of October 2020. Our experts will present the new European regulation on post-marketing surveillance of medical devices and will discuss the following points:
– How to set up post-marketing surveillance of MDs and what data to monitor?
– How is incident reporting carried out?
– What are the periodic reports to be written, for what purpose and what do they contain?
– How to set up a risk management plan?