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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 register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How to conform with the legal requirements for placing medical devices on the market.
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
How to comply with the regulatory requirements for manufacturing custom-made medical devices.
Find out when it's possible to get zero-rated supplies on medical and research goods and services that have been funded by charities.
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