Danish agency take action to support European database:
This article was originally published in Clinica
Executive Summary
The Danish Medicines Agency, the regulatory authority for medical devices, is writing to all local manufacturers and authorised representatives to encourage them to register via the European medical device database, EUDAMED, which has just become fully operational (see Clinica No 1090, pp 1-2). It is also planning to register all medical devices, starting with class I.