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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
Waste electrical and electronic equipment (WEEE) - retailer and wholesaler responsibilities, waste collection and compliance schemes.
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
How to use a cost utility analysis to evaluate your digital health product.
Information on road traffic devices, such as breath-testing, speed cameras and immobilisation devices.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
Information for manufacturers, healthcare professionals, researchers and patients on software as a medical device (SaMD) and AI as a medical device (AIaMD).
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
What to do if a laptop or tablet you’ve received from a DfE programme is not working.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
Medicines and Healthcare products Regulatory Agency (MHRA) guidance on using medical devices safely.
Research detailing cyber security issues in internet-connected devices used by businesses and organisations.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Posters and leaflets about using medical devices safely for healthcare professionals.
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