Consultation on the future regulation of medical devices in the United Kingdom

Consultation on the future regulation of medical devices in the United Kingdom The MHRA is inviting members of the public to provide their views on possible changes to the regulatory framework for medical devices in the United Kingdom. The MHRA wants to develop a future regime for medical devices which enables: improved patient and public safety; greater transparency of regulatory decision making and medical device information; close alignment with international best practice and; more flexible, responsive and proportionate regulation of medical devices. It welcomes the views of patients, medical device researchers, developers, manufacturers and suppliers, clinicians, other healthcare professionals and the wider public to help shape the MHRA’s future approach to regulating medical devices in the UK. This consultation closes on 25 November 2021. Medicines and Healthcare products Regulatory Agency