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 on February 6, 2019 at Nippon Hotel in Istanbul

The training was organized as part of a 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, organizations offering testing, evaluation, analysis and certification services, and relevant stakeholders with the coordination of the Ministry of Trade.

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