The COEN group, responsible for market surveillance published in cooridination with Swissmedic, A guidance related to the instructions for use (IFU) of resterilisable medical devices. This guidance is an user-friendly tool with checklists to help complying with ISO 17664. COEN_IFU-resteri-CL_EN-ISO17664_EN-ISO14937_v1.0

pilot program to test a common electronic submission format for reviewing device submissions: 4 notified bodies members of Team-NB joined the pilot program (namely BSI, MDC, NSAI and TÜV SÜD).      

concerning the proposals prepared by the Latvian presidency and published by the Council of the European Union concerning the new medical devices regulations.