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Register to vote Register by 18 June to vote in the General Election on 4 July.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
Information about the EU Regulations and their implementation in Northern Ireland
An overview of the future requirements for rapid COVID-19 diagnostic assays for antigen lateral flow devices.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Guidance for local authorities, trusts, schools, colleges and FE institutions about who owns DfE loaned devices, asset management and loan agreements.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to conform with the legal requirements for placing medical devices on the market.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Check the tariff classification for four-wheeled vehicles powered by an electric motor fitted with a hydraulic lifting device and telescopic jib.
Information and guidance on a range of medical devices for users and patients.
How to get fast-track approval of medical devices during COVID-19.
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.
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