Our virtual meeting proposes the actions medical device manufacturers could take to strengthen the implementation strategy for EU MDR and IVDR. The expert speakers will share all the different ways to prepare your company and team for a smooth transition; update your QMS for EU MDR; meet Notified Body expectations during the audit; comply with requirements for vigilance reporting and post-market surveillance; review labeling and packaging challenges under updated UDI; evaluate strategies to remediate gaps in clinical data and more.