New regulations to enhance the UK’s ability to benefit from rapidly advancing assistive technology
A new roadmap has been set out for the development of new and robust regulations for medical devices in the UK, which includes assistive technologies…
Manufacturers given more time to get certain medical devices CE certified
The EU has taken steps to give manufacturers more time to get certain medical devices, which includes certain assistive technologies, certified under the EU Medical…
MHRA seeks views of researchers, suppliers and users of medical devices to inform future regulation
People are being encouraged to contribute their views to a public Medicines and Healthcare products Regulatory Agency (MHRA) consultation on changes to how medical devices…