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.
It is welcoming 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
Survey by Medicines and Healthcare Regulatory Agency.