Silvia Anghel

Silvia Anghel is a seasoned professional in the field of In Vitro Diagnostics (IVD), currently serving as Sr Director of Quality & Regulatory Affairs at Veranex since July 2022. Previously, Silvia held multiple senior roles at Medidee, including Senior Consultant and Head of the Medidee IVD Group, where responsibilities encompassed regulatory strategies, technical documentation, and quality management systems (QMS) aligned with ISO standards. Other experience includes RA & QA Manager at ECS-progastrin, Senior Scientist and Regulatory Head at Augurix Diagnostics, and various research positions in prominent academic institutions. Silvia possesses extensive expertise in oncology, metabolism-related disorders, and gastroenterology, coupled with a solid track record in project management, clinical trial support, and the implementation of regulatory requirements across diverse projects. Educational qualifications include a PhD in Molecular Biology & Genetics from the University of Geneva and multiple certifications in clinical research and medical device auditing.