The safe operation of medical devices is a shared responsibility between the manufacturers, health care centres and the users, while the Competent Authorities have the responsibility for the implementation of the EU Directives, as well as the notification and evaluation of adverse incidents. Member States are called to adjust their practices in accordance to the Directives and set up the mechanisms required for the proper and effective operation of the Vigilance System for Medical Devices.
Odos Stadiou, Platani, 265 00 Rio, Patras, Greece
Tel. +30 2610 911590 911591, Fax. +30 2610 911592