Biochemist and Pharmacist from the University of Buenos Aires, Master's Degree in Regulatory Sciences of Health Products; with 20 years of experience in Quality Assurance and 14 years in Regulatory Affairs in IVD Medical Devices. Since 2019, I have led the In Vitro Diagnostic Medical Devices Office in ANMAT. I lead the IVD pre-market approval department. Representative of ANMAT in conferences and international collaboration projects as a specialist on the subject (such as MERCOSUR and the WHO IVD prequalification group), and I also participate in IMDRF´s working groups.