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Dia Pro Medical Devices Regulation training

Dia Pro successfully completed MDR 2017/745 Technical Documentation Training.


Medical device directives (93/42/EEC), have been removed by The Europian Union Medical Devices Commission. In May 5, 2017, MDR has been published in EU official newspaper. 

Meanwhile, to determine our road map and complete the regulation’s mandatories, our company has been completed MDR 2017/745 technical documentation training succesfully.