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Register to vote Register by 18 June to vote in the General Election on 4 July.
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 the MHRA makes decisions on what is a medicinal product (borderline products).
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
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.
Information for manufacturers, healthcare professionals, researchers and patients on software as a medical device (SaMD) and AI as a medical device (AIaMD).
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
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).
Chief Medical Officer for England, Professor Chris Whitty's annual reports and lectures on medicine and public health.
Order a certificate of free sale to export medical devices outside the UK.
Advice for medical professionals for assessing fitness to drive.
Medicines and Healthcare products Regulatory Agency (MHRA) guidance on using medical devices safely.
This notice advises what medical conditions are required to be reported on during the validity of an ENG1 medical certificate.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
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 .
UK Visas and Immigration guidance on handling medical issues of visa applicants.
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
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