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Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
Order a certificate of free sale to export medical devices outside the UK.
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
The MHRA has conducted a thorough assessment of technical and biological safety information provided by NSO and is satisfied that the modified MAGEC X system can now be used in the UK.
Checklists providing a practical guide to using medical devices.
Information on when software applications are considered to be a medical device and how they are regulated.
Guidance on what approved bodies are, what they do and how you can become one.
Home Office approved drug-testing devices.
Report on all regulations in force during the first reporting period made using the powers in specific sections of the act, including stakeholder feedback and the department’s response.
The MHRA welcomes the publication of Dame Margaret Whitehead’s Equity in Medical Devices: Independent Review
UK approved bodies listed under Medical Devices Regulations 2002 (SI 2002 No 618, as amended) (UK MDR 2002).
We're looking for your views on how medical devices will be regulated across the United Kingdom (UK) in the future.
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
Posters and leaflets about using medical devices safely for healthcare professionals.
For waste operators and exporters classifying some waste electrical and electronic equipment (WEEE) devices, waste components, and wastes from their treatment.
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
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