Following the Brexit, after October 31, 2019, the Great Britain will become a third country vis-à-vis the EU.
According to the regulation defined by the MHRA, to continue to put devices on the territory it will be necessary to appoint a representative on site.

In this respect, for Manufacturers based outside the United Kingdom, MGRA created a new role in the regulation of Medical Devices and IVD, known as UK Responsible Person. This entity has its registered office in the United Kingdom and it acts on behalf of the Manufacturer to perform specific tasks, such as the registration of Medical Devices at the Regulatory Authority before they are placed on the British market.

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