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Patients in the UK and Singapore could gain faster access to cutting-edge healthcare innovations under a new partnership bringing two globally respected regulators together with one of the world’s leading biotech creators.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
How the MHRA makes decisions on whether a borderline product is a medical device and which risk class should apply.
Developers work with the NHS, the medicines regulator and the UK health technology assessment bodies from the early stages of clinical development, as part of the Innovative Licensing and Access Pathway.
How to use a quasi-experimental study to evaluate your digital health product.
New government funding will help make the boldest ideas in UK life sciences a reality.
Information about the Release of Data Fund and Breakthrough Fund, and details of how to apply.
A British AI-driven innovation that dramatically speeds up the development of materials used in wind turbines and electric vehicle batteries has won the UK government’s £1 million Manchester Prize.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
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