Consultant with over 10 years’ experience, specialised in regulatory affairs for medical devices, in vitro diagnostics, borderline products, drug-device combinations and CMC aspects of medicinal products. Speaker on EU regulations for MDs and IVDs and lecturer at degrees (Bioengineering – UPF), postgraduate programs (Biotech and Pharmaceutical Industry – IQS, dHEALTH Barcelona – MOEBIO) and innovation accelerator programs for medtech entrepreneurs (CIMTI, CaixaImpulse, CRAASH Barcelona, among others). Leader of the MD team at Asphalion S.L. Prior to starting her career path in regulatory affairs, Dominique Monferrer did a PhD in Protein X-ray Crystallography at the Spanish National Research Council (CSIC). She graduated in Human Biology at University Pompeu Fabra in Barcelona (Spain).