Stefania Fortunato

Stefania Fortunato is a consultant specializing in medical devices and in vitro diagnostic medical devices at PQE Group since March 2021, with expertise in EU MDR 2017/745 and EU IVDR 2017/746. Prior experience includes roles as a Quality Assurance & Regulatory Affairs Specialist at GVS Filter Technology Italy, where responsibilities involved reviewing technical documentation for compliance with the new MDR, and as a Quality Assurance & Quality Control professional at GreenBone Ortho s.r.l. Previous positions also include support in Healthcare Management & Medical Devices databank at Siemens Healthcare and participation in a scientific-informatics project at Exprivia. Stefania completed an internship in Environmental Biochemistry at Università degli Studi di Milano-Bicocca, holds a degree in Regulatory Affairs from ALMA LABORIS Business School, and has a Master’s in Diagnostic Imaging Systems. Educational background includes studies at the Liceo Scientifico Statale "Enrico Fermi."