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How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Gillian Keegan discusses the importance of digital skills and artificial intelligence at London Tech Week
Guidance for manufacturers, importers and distributors.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Get help to classify footwear and parts of footwear for import and export.
Applications are now open for Integrated care systems to apply for a share of £30 million to roll out innovative technology
Guidance and support on coronavirus (COVID-19) in Wales.
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.
Find out which supplies of children’s clothing or footwear are zero-rated for VAT.
A collection of documents relating to the government's policy on app security and privacy.
List of manufacturers and their medical devices which have been granted an exemption by the MHRA. The list also includes manufacturers whose exemption expired or was cancelled. This information will be listed for 2 months after expiry or cancellation.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
How to begin with evaluating a digital health product, including when to evaluate, budgeting and getting support.
Engage with the Ministry of Defence (MOD) on SKYNET Enduring Capability (SKEC), the next generation of solutions for future satellite communication programmes.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
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