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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 to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
Steps to help grow your business - finding finance, mentors, increasing sales and developing products and services
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Information about the EU Regulations and their implementation in Northern Ireland
Information and guidance on a range of medical devices for users and patients.
How to apply to provide digital technologies under the Help to Grow: Digital scheme if you're a software vendor.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
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.
Guidance for local authorities, trusts, schools, colleges and FE institutions about who owns DfE loaned devices, asset management and loan agreements.
Guidance for manufacturers, importers and distributors.
Order a certificate of free sale to export medical devices outside the UK.
Information on road traffic devices, such as breath-testing, speed cameras and immobilisation devices.
Advice for manufacturers of Class I medical devices for placing products on the UK market
How to get fast-track approval of medical devices during COVID-19.
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