Join us on 16th - 17th June online to master the art of crafting Standard Operating Procedures (SOPs) within regulated environments.
More information
RQA membership is a great way to connect with your QA colleagues.
More information
Join the community - networking, discussion and more. Open to all.
More information
Could you write an interesting article for the RQA community?
More information15th May 2026
Summary:
The Medicines and Healthcare products Regulatory Agency (MHRA) has launched a consultation on proposed updates to the UK’s medical device regulatory framework. The changes aim to improve patient safety, support innovation and ensure the UK remains an attractive market for medical technology. Proposals include enhanced pre and post market requirements, stronger oversight of high risk devices and greater transparency around device performance. The consultation also considers how the UK system can better respond to emerging technologies while aligning, where appropriate, with international standards. Stakeholders across healthcare, industry and research are encouraged to provide feedback to help shape the future regulatory approach.