Medical device safety: IMQ has been appointed as the notified body for the new European Regulation
The notification, that was published on the 20th of August in the European NANDO system, allows IMQ to support right now medical device manufacturers in getting certification under the new MDR Regulation. The MDR – which will become mandatory as of the 26thof May and will replace the old Directives (93/42/EEC and 90/385/EEC) – is […]