Eudamed: Introduction to Its Gradual Implementation

A New Standard for Transparency and Traceability in Medical Devices Regulation (EU) 2024/1860 has introduced significant changes to MDR (EU) 2017/745 and IVDR (EU) 2017/746, facilitating the gradual implementation of Eudamed, the European database on medical devices. This system marks a crucial step towards greater transparency, traceability, and safety in the healthcare sector. Since July…

GFI obtains registration on the EUDAMED portal

EUDAMED: Gruppo FarmaImpresa achieves registration as a Manufacturer and Producer of Procedural Systems/Kits In recent years, the European Union has shown a growing concern for the safety and effectiveness of medical devices used within the European market. To enhance monitoring and ensure stricter control of these devices, the European Commission has developed EUDAMED (European Database…