Aida I.

Aida I. is a Senior Quality and Regulatory Affairs Specialist and PRRC with over a decade of experience in the medical devices and in-vitro diagnostics sectors. They have worked in various roles including technical writer, regulatory expert, and project leader, focusing on ISO 13485 compliance and CE marking. Aida holds a B.Sc in medical engineering from the Royal Institute of Technology (KTH) and is an active member of the Swedish standardization committee TK-344 Health Informatics. Currently, Aida acts as Senior Quality and Regulatory Affairs Specialist at Inera AB, overseeing Quality Management System compliance and ensuring regulatory adherence prior to product release.