Eucomed, the European Medical Technology Industry Association, welcomes the approval by the Regulatory Committee on Medical Devices of the draft Regulation on electronic instructions for use (IFUs) of medical devices. Electronic IFUs (or e-labels) have the potential to not only improve patient safety and reduce the medical technology industry’s environmental impact, but also to ensure that the correct IFUs are available at the right time in the right place, while facilitating their storage.
EBA, the European Blood Alliance, Eucomed, the European medical technology industry association, the European Commission and Competent Authorities met on 18 June to discuss the harmonization of apheresis, collection technology for blood donors and patients, connectors and to promote Managed Convergence, an active collaboration between stakeholders.