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

The MHRA is inviting members of the public to provide their views on proposed changes to the regulatory framework for medical devices in Great Britain (England, Scotland and Wales).  
 
MHRA 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 closes at 11:59pm on 5 January 2025

Click here to take part