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List of Field Safety Notices from 22 to 26 April 2024.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Medicines and Healthcare products Regulatory Agency (MHRA) guidance on using medical devices safely.
How to apply for repayment of import duty and VAT on protective equipment or medical supplies brought into the UK from non-EU countries from 30 January 2020 up to 31 December 2020.
The MHRA welcomes the publication of Dame Margaret Whitehead’s Equity in Medical Devices: Independent Review
Advice for manufacturers of Class I medical devices for placing products on the UK market
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.
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 a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
How to get fast-track approval of medical devices during COVID-19.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
Guidance on decontamination and infection control, including surgical instruments, dental equipment, endoscopes and benchtop steam sterilizers.
The MHRA has today set out its strategic approach to artificial intelligence (AI)
How to use a case-control study to evaluate your digital health product.
How to conform with the legal requirements for placing medical devices on the market.
Monitoring significant occupational exposures to HIV, hepatitis B and hepatitis C in healthcare workers, and advising on avoiding injuries.
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