Andrea Larrañaga Pérez

Andrea Larrañaga Pérez is a skilled Regulatory Affairs Specialist with extensive experience in the medical devices and in vitro diagnostic sectors. Currently employed at Zwiers Regulatory Consultancy BV, responsibilities include contributing to regulatory strategic activities and reviewing technical documentation related to MDR/IVDR compliance. Previous roles include Associate Manager at Veristat, where management of regulatory affairs staff and establishment of Regulatory Affairs Europe were key duties, and Regulatory Affairs Manager at DDR is Now Veristat, focusing on strategic analyses and procedures under MDR/IVDR. Andrea has a solid technical background, holding an MSc in Biomedical Engineering with a specialization in Medical Devices from the University of Groningen and a BSc in Biomedical Engineering from the University of Navarra.