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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.
How the MHRA makes decisions on whether a borderline product is a medical device and which risk class should apply.
Pioneering defence firms have pitched their innovations directly to major investors in a first-of-its-kind Dragons’ Den-style event, set up by the Ministry of Defence.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
How to use a quasi-experimental study to evaluate your digital health product.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Information about the Release of Data Fund and Breakthrough Fund, and details of how to apply.
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.
Foresight project looking at the scientific and technological areas that could transform the UK economy in the future.
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