ABOUT THE COURSE

This webinar offers practical insight into the UK MHRA’s Manufacturer’s On-line Reporting Environment (MORE) platform. It will provide in-depth guidance on how to answer certain elements, covering all forms of incident and other reports which must be notified by manufacturers to the MHRA in the event of an alleged adverse incident involving a medical device. Special notification, for example originating at market surveillance, will also be covered.

Dedicated e-learning modules are presented on manufacturer’s incident reports, market interventions by manufacturers and other topics.