Service contract to translate and validate the European medical device nomenclature (EMDN) and the International medical device regulators forum (IMDRF) adverse events terminologies in official EU languages

ncludes the review and harmonisation of the existing translated versions of the EMDN and the translation and validation of the seven IMDRF AE terminologies to EU official languages. Specialised expertise in the medical sector (medical devices and clinical aspects) is necessary to conduct both tasks.

This action aims at facilitating the use of European harmonised medical device nomenclatures (EMDN) and the International medical device regulators forum’s adverse event (IMDRF AE) terminologies by all stakeholders. It i