MedTech Innovation News 31 March 2021
- Following Brexit and the subsequent passing of The Medicines and Medical Devices Act 2021 (or M&MD), the UK now has a new framework for regulating medical devices. Part of this was from 1st January 2021 all medical devices placed on the market need to be registered by their suppliers on the MHRA’s Device Online Registration System (DORS), as part of a UK-wide Medical Device Information System (MDIS).
