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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.
The Medical Research Council (MRC) is a national funding agency dedicated to improving human health by supporting research across the entire spectrum of medical sciences, in universities and hospitals, in MRC units, centres and institutes in the UK, and in...
The use of ionising radiation in medicine, including recommended dose measurements and guidance on safe radiology practice.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Order a certificate of free sale to export medical devices outside the UK.
Chief Medical Officer for England, Professor Chris Whitty's annual reports and lectures on medicine and public health.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
This notice advises what medical conditions are required to be reported on during the validity of an ENG1 medical certificate.
UK Visas and Immigration guidance on handling medical issues of visa applicants.
Posters and leaflets about using medical devices safely for healthcare professionals.
The Medicines and Healthcare products Regulatory Agency (MHRA) has today (9 May 2024) launched AI Airlock, its new regulatory sandbox for AI as a Medical Device (AIaMD).
Medicines and Healthcare products Regulatory Agency (MHRA) guidance on using medical devices safely.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Advice for manufacturers of Class I medical devices for placing products on the UK market
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.
Visit the UK for medical treatment - check if you’re eligible and if you need a visa, what visa to apply for, what to do when you travel to the UK.
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
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