Webinar "Changes to the MDR and IVDR regarding transitional provisions - Deadlines and what I should do."

In this webinar we explore the evolution of Medical Device regulations in Europe, from the transition from directives to regulations to the main changes in Regulation (EU) 2023/607 (MDR). We discuss the importance of effective implementation, the challenges facing the industry and the European perspective on mitigating restrictions. Additionally, we address relevant guidelines, specific challenges in Portugal and changes to the In Vitro Diagnostic Medical Devices (IVD) Regulation.