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How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Visit the UK as a Standard Visitor for tourism, business, study (courses up to 6 months), medical treatment and other activities. Find out whether you need a Standard Visitor visa, or can visit without a visa.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Apply for the Registered Traveller service to get through UK border control faster and without filling in a landing card
Find out about the Industry Security Assurance Centre (ISAC) and its associated responsibilities.
Food and drink labelling and packaging regulations - what you must show, warnings, health and organic labels and packaging standards.
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