Dominique has more than twenty years of experience in medical devices acquired in pharmaceutical and biomedical industries. Working successively in R&D, Global Marketing, Medical Affairs, and Regulatory Affairs, she has led cross-functional projects in an international and multicultural environment.
In her previous position, she managed multiple client projects, supporting the development of medical devices, and developing client regulatory and clinical strategies.
She obtained a Res MSc in Neurosciences, and an MS in Strategic Information Management from University Claude Bernard of Lyon.
She specialized in Technical and Regulatory Affairs for Medical Devices (MSc) from ISPB and Polytech Lyon, and in Clinical Trials Interpretation (DU) from University of Medicine of Lyon, to face the critical challenges of regulatory requirements in medical device development.