Register Medical Devices to Place on the Market

On 28 July 2022 the MHRA updated the guidance on registration of medical devices.

All medical devices, including IVDs, custom-made devices and systems or procedure packs, must be registered with the MHRA before they can be placed on the market in Great Britain (England, Wales and Scotland).

The updated version added new section 'Coronavirus Test Device Approval (CTDA) and Registering with MHRA'.

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