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Register to vote Register by 18 June to vote in the General Election on 4 July.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
This guidance is designed to help UKHSA customers and partners to navigate engaging and working with us and to signpost upcoming events and opportunities.
Home Office approved drug-testing devices.
Find out when it's possible to get zero-rated supplies on medical and research goods and services that have been funded by charities.
The MHRA welcomes the publication of Dame Margaret Whitehead’s Equity in Medical Devices: Independent Review
Information for manufacturers, healthcare professionals, researchers and patients on software as a medical device (SaMD) and AI as a medical device (AIaMD).
Check the legal requirements you need to meet before you can place a medical device on the market and see how MHRA monitors compliance.
How to get fast-track approval of medical devices during COVID-19.
The Medicines and Healthcare products Regulatory Agency (MHRA) has designated three new UK Approved Bodies, almost doubling the UK’s capacity to certify medical devices, supporting faster certification of safe and effective medical devices for healthcare professionals and the public.
Information on taking, submitting and processing samples which potentially contain monkeypox virus.
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
How the supply of medical devices from Great Britain into Northern Ireland works.
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