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Detailed guidance, regulations and rules
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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.
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Information on when software applications are considered to be a medical device and how they are regulated.
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.
Get help classifying computers, inkjet and toner cartridges and their components.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Information and guidance on a range of medical devices for users and patients.
Get help to classify various types of vehicles such as mobility scooters, dumpers and utility vehicles, all-terrain vehicles and e-bikes for import and export.
Get help to classify drones and aircraft parts for import and export.
Guidance for local authorities, trusts, schools, colleges and FE institutions about who owns DfE loaned devices, asset management and loan agreements.
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