Argos Multilingual
4 min. read
Medical device manufacturers (MDMs) have various resources to ensure compliance with the EU Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR). Recently, the EU extended these deadlines, giving manufacturers more time for compliance. For instance, conformity assessments for higher-risk devices (class IIb and class III) are now due in 2027, while lower-risk devices […]





