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What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Medicines and Healthcare products Regulatory Agency (MHRA) guidance on using medical devices safely.
Guidance for manufacturers on the regulations that apply to prosthetic, orthotic and ophthalmic devices.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
Information about the EU Regulations and their implementation in Northern Ireland
How the supply of medical devices from Great Britain into Northern Ireland works.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Check the legal requirements you need to meet before you can place a medical device on the market and see how MHRA monitors compliance.
Information on MHRA's enforcement duties and how to report a non-compliant medical device.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
Advice for manufacturers of Class I medical devices for placing products on the UK market
UK approved bodies listed under Medical Devices Regulations 2002 (SI 2002 No 618, as amended) (UK MDR 2002).
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Guidance on what approved bodies are, what they do and how you can become one.
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