The Training Program on the Medical Devices Regulation (MDR 2017/745), the In-Vitro Diagnostic Medical Devices Regulation (2017/746/EU), the Directive Concerning Medical Devices (93/42/EEC) was conducted at İzmir Anemon Hotel

6 March 2019

The training program was organized with the coordination of the Ministry of Trade as part of the project on Awareness Raising in the Areas of Product Safety, Market Surveillance and Conformity Assessment. The program saw great participation from manufacturers, distributors, importers, exporters and relevant stakeholders.

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