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Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Information about the EU Regulations and their implementation in Northern Ireland
Advice for manufacturers of Class I medical devices for placing products on the UK market
Using an ecological momentary assessment to evaluate your digital health product.
Apply for a grant-aided vessel monitoring system, register or re-register your device, and guidance for manufacturers and engineers.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Guidance for driving examiners on particular types of vehicle and adaptations.
Find out about the VAT place of supply rules if your business sells digital services to private consumers.
Information and guidance on a range of medical devices for users and patients.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Get help classifying computers, inkjet and toner cartridges and their components.
Environment Agency regulatory position on using devices intended to hook fish automatically, in breach of Thames byelaws.
Check the tariff classification of multifunctional display-monitors for vehicles.
How to use a micro-randomised trial to evaluate your digital health product.
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