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Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
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Data, Freedom of Information releases and corporate reports
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
Help available and steps you should take if you have a medical emergency or are hospitalised abroad, including for planned treatment.
Food and drink labelling and packaging regulations - what you must show, warnings, health and organic labels and packaging standards.
To sell food and drink products, the label must be: clear and easy to read…
You must show the following information: the name of the food a ‘best…
If your food or drink product has 2 or more ingredients (including any…
You must show an appropriate warning on the label if your food contains…
Nutrition labelling You must follow nutrition labelling information rules…
If you’re a retailer, you can label products ‘organic’ as long as: at…
Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
Guidance for prescribing vets on the use of the cascade.
Information about medical devices that the public can buy for personal use and how we make sure they are safe and effective.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Data security control principles to use when processing and sharing personal data in your service.
Guidance for chief police officers when considering applications for the early deletion of DNA profiles, fingerprint records and Police National Computer records.
How to conform with the legal requirements for placing medical devices on the market.
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