Open Consultation | Consultation on Medical Devices Regulations
The Medicines and Healthcare products Regulatory Agency (MHRA) is inviting members of the public to provide their views on proposals to update the regulatory framework for medical devices.
We welcome the views of patients, medical device researchers, developers, manufacturers and suppliers, clinicians, other healthcare professionals and the wider public on four areas:
- International reliance
- UKCA marking
- In vitro diagnostic devices
- Assimilated EU law
This consultation applies to medical devices in Great Britain. For guidance on the regulation of devices in Northern Ireland, see Regulation of devices in Northern Ireland.
This consultation closes at 11:59pm on 5 January 2025
For all information, including how to respond, please click the button below:
