EUROPEAN COMMISSION EXPERT PANELSON MEDICAL DEVICES AND IN VITRO DIAGNOSTIC DEVICES
En son güncellendiği tarih: 28 Ağu 2019
Call for clinical and other experts to be published later in 2019!
The new EU regulations on medical devices and in vitro diagnostics came into force in 20171 . They stipulate the establishment of expert panels to support the assessment of specific high-risk devices and to contribute to the prospective improvement of the overall framework by advising the Commission, the Medical Device Coordination Group, Member States, Notified Bodies and manufacturers.