On Tuesday 23 September, MedTech Europe, alongside other industry organisations at European level, welcomed the European Commission’s commitment to revise the rules on medical devices (MDR) andin vitro diagnostic medical devices (IVDR) by the end of 2025.
It is essential to ensure that patients have “continued access to safe and effective medical technologies”, the association stresses in a letter sent on 19 September to the European Commissioner for Health, Olivér Várhelyi.
The...