Translation in all EU official languages of the European medical device nomenclature and of the International medical device regulators forum’s adverse events terminologies

ncludes the review and harmonisation of the existing translated versions of the EMDN and the translation and validation of the seven IMDRF AE terminologies from English to the 23 other EU official languages. Specialised expertise in the medical sector (medical equipment and clinical aspects) is nece

ssary to conduct both tasks.