Universal Medica have hosted its next live webinar on Friday 23 October 2020 at 2:30pm on the topic of medical device vigilance. Our experts presented the new European regulation on post-marketing surveillance of medical devices and addressed the following points:
– How to set up post-market surveillance of medical devices and which data to monitor?
– How does incident reporting work?
– What are the periodic reports to be written, for what purpose and what do they contain?
– How to set up a risk management plan?
