Senior Regulatory Consultant, IVD
Namsa
Christèle obtained her PhD in Cellular Biology from University of Joseph Fourier, Grenoble (France). She is very interested in applied research and health, and has worked for several years on projects for the development of In Vitro diagnostic devices (oncology, virology ...) before completing a University Diploma in Clinical Research at the Faculty of Medicine of Marseille. As MD & IVD consultant, she is involved in ensuring compliance with classification, technical documentation for CE marking, performance evaluation within the framework of IVDD and IVDR, regulatory support and PMS.
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UK Market: PMS and Vigilance Requirements for IVDs
Tuesday, May 7, 2024
11:30 – 12:00 CEST