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Information and guidance on a range of medical devices for users and patients.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
Order a certificate of free sale to export medical devices outside the UK.
Guidance for UK wholesalers and manufacturers on how to import human medicines including unlicensed medicines, how to apply for a licence and how much it costs.
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.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Guide for overseas investors on how to access NHS procurement channels.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to register with an NHS doctor and patient questionnaires in Ukrainian and Russian.
If you’re travelling abroad, it's important to take out appropriate travel insurance before you go.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Over two million doses of illegally traded medicines valued at almost £5m seized so far this year.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Find out when it's possible to get zero-rated supplies on medical and research goods and services that have been funded by charities.
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
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