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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
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
What to do if a laptop or tablet you’ve received from a DfE programme is not working.
A buyer's guide for mobile devices, which outlines 7 areas that consumers should check for when choosing or using their mobile device.
Order a certificate of free sale to export medical devices outside the UK.
Research detailing cyber security issues in internet-connected devices used by businesses and organisations.
Information on road traffic devices, such as breath-testing, speed cameras and immobilisation devices.
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
There are a number of high cost devices that are excluded from the Payment by Results (PbR) tariff.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Medicines and Healthcare products Regulatory Agency (MHRA) guidance on using medical devices safely.
UK approved bodies listed under Medical Devices Regulations 2002 (SI 2002 No 618, as amended) (UK MDR 2002).
Advice on writing clear notices and maximising replies to your FSNs.
For waste operators and exporters classifying some waste electrical and electronic equipment (WEEE) devices, waste components, and wastes from their treatment.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Guidance for healthcare professionals covers the use, management and safety of in vitro diagnostic (IVD) devices, including blood glucose meters.
Information on when software applications are considered to be a medical device and how they are regulated.
Posters and leaflets about using medical devices safely for healthcare professionals.
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