MHRA - Consultation on Medical Devices Regulations: Routes to market and in vitro diagnostic devices

14th November 2024

MHRA - Consultation on Medical Devices Regulations: Routes to market and in vitro diagnostic devices

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. 

The views of patients, medical device researchers, developers, manufacturers and suppliers, clinicians, other healthcare professionals and the wider public on four areas (below) are welcomed.

• International reliance 
• UKCA marking 
• In vitro diagnostic devices 
• Assimilated EU law.

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