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Data, Freedom of Information releases and corporate reports
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Resources to help local commissioners achieve value for money by estimating the return on investment (ROI) and cost-effectiveness of public health programmes.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
Information for British people on medical support in Thailand including mental health, lists of hospitals and care homes and how the British embassy can help.
Practical materials for primary and secondary schools to use to train staff to teach about basic first aid.
Information and guidance on a range of medical devices for users and patients.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Get a medical certificate to work at sea - ENG 1 or ML5 medical certificates, how much they cost, how to apply.
How to conform with the legal requirements for placing medical devices on the market.
A development programme of educational resources on critical public health topics for people who work in the health and care sector and the extended public health workforce.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Chief Medical Officer for England, Professor Chris Whitty's annual reports and lectures on medicine and public health.
How to use a cost utility analysis to evaluate your digital health product.
Supporting health and care professionals to improve services by better understanding the health outcomes that some people in the Roma community face.
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