Rosalie Muscat

Rosalie Muscat is a highly experienced professional in the field of medical device regulatory affairs. Currently serving as a Senior Consultant at RQM+ since January 2021, Rosalie manages the upgrade of clinical documentation from the Medical Device Directive (MDD) to the Medical Device Regulation (MDR), coordinates routine updates based on risk classification, and supports clients through effective communication and project management. Prior to this role, Rosalie held positions as Capability Manager and Senior Associate at MAETRICS and worked as a Medical Writer at Baxter Healthcare Corporation, contributing to regulatory submissions and documentation updates for a range of medical devices. With an MSc in Medical Technology Regulatory Affairs from the University of Galway and a Bachelor of Education from the University of Malta, Rosalie possesses a strong educational foundation combined with hands-on experience across various medical device classifications.