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Laura Zucchelli, MSc in Biomedical Engineering, has over 9 years of experience in the biocompatibility of medical devices. Starting at Eurofins as Study Director for biocompatibility studies, she was in charge of study design definition and customisation, to satisfy the device’s needs and customer’s expectations. Within her journey at Eurofins, she has held different roles, such as Team Leader, Project Manager, and Laboratory Manager gaining broad experience within the Medical Device and Pharmaceutical fields. In her current position, she is in charge of leading the Medical Device Business Unit with a strong focus on Biocompatibilities testing covering microbiological in vitro, in vivo, and chemical laboratories. Over the past year, she has followed and successfully achieved ASCA accreditation for biocompatibility tests, working deeply with FDA's dedicated team. She is a member of ISO TC 194 where she is particularly active within WG1,7,8,10,16 paying high attention to in vivo/in vitro test transition.