Just released – a DRAFT MDCG on Questions and Answers on Trend Reporting as Outlined in the Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746 on in vitro diagnostics medical devices: https://ec.europa.eu/transparency/expert-groups-register/core/api/front/document/121204/download

Excited to see this as I think this is something that manufacturers consistently struggle with – understanding how to identify trends and when to report them. I am curious as to whether this is an open draft where there is an opportunity to provide feedback – @AmieSmirthwaite would you have any insight into this (or anyone else in the iM community?!)