Emily McLucas is a Quality & Regulatory Consultant at Vetex Medical. Emily has over 14 years’ experience working in the medical device sector developing products across the risk spectrum from Class I to Class III.
Emily has worked in regulatory, clinical and design assurance roles in multi-national and start-up companies bringing devices from concept to market.
At Vetex, Emily’s main areas of focus are regulatory strategy development, submissions and compliance, risk management and design assurance.
Emily has a PhD in Biomedical Science from NUI, Galway.