Mapping medical device regulations

By Trilogy Writing & Consulting

The implementation of the EU’s Medical Device Regulation (MDR) 2017/745 has been delayed, having had a scheduled date of 26 May 2020. Because of the Covid-19 pandemic and the sudden increase in demand for specific medical devices, the date has been moved to 26 May 2021. This relieved pressure has been felt across the sector by manufacturers and regulators alike, as the 2020 implementation date approached amid a climate of uncertainty. Trilogy Writing & Consulting, a company that focuses on clinical regulatory documentation, discusses the importance of key terminology surrounding EU medical device requirements.

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