Nina Mavc is a Regulatory Affairs Manager and PRRC at CERHUM, leveraging over a decade of expertise in the MedDev and IVD industry to navigate regulatory, quality, and clinical compliance challenges. Since 2024, Nina has played a pivotal role in advancing healthcare products by ensuring they meet stringent regulatory standards. Previously, Nina held key positions at DIAsource ImmunoAssays® S.A. and Graftys, focusing on regulatory compliance and lifecycle management. Nina has also contributed to consulting and business development in the field, providing critical know-how that fosters innovation. Nina earned a BSc in Microbiology from the University of Ljubljana and a university certificate in clinical, regulatory, and quality affairs from Ecole Polytechnique de Louvain.
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