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Dr. Flore Delaygue is a Consultant with over 6 years of experience specialising in biocompatibility of medical devices and is a member of the Eurofins Medical Device Testing consultancy team. After completing a PhD in biology in 2016, Dr. Flore Delaygue began working as a Study Director for biocompatibility study programmes (comprising of all programme elements from study design to data analysis, data interpretation and report writing), performing mainly in vitro hemocompatibility testing, in vivo long-term systemic toxicity studies and evaluating local tissue effects post implantation, under ISO 10993 standards and GLPs. In March 2023, Dr. Flore Delaygue joined the Eurofins Medical Device Testing consultancy team to lead medical device biological risk assessments and related dedicated training programmes.