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The New Medical Device Regulation (MDR) and the End User: Supporting Usability Through Documentation

The medtech industry is undergoing significant change, from the introduction of the new MDR to the growth of home-based healthcare and the uncertainties of Brexit. At some recent Irish medtech events, the major topics dominating conversation were: Regulation 2017/745 on Medical Devices – widely known as the MDR Usability and the importance of the end […]

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