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Register to vote Register by 18 June to vote in the General Election on 4 July.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
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 the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to get fast-track approval of medical devices during COVID-19.
How to conform with the legal requirements for placing medical devices on the market.
Information on cleaning an oil spill including your options, how to get a product approved and how long it will take.
Information about the EU Regulations and their implementation in Northern Ireland
Information on content filtering and mobile device management to ensure devices are safe to use by young people and families
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
An overview of the future requirements for rapid COVID-19 diagnostic assays for antigen lateral flow devices.
How schools should setup a Microsoft Windows laptop or tablet before lending the device to a child, family or young person.
Find out which sanitary protection products you can supply at the zero rate of VAT.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
For waste operators and exporters classifying some waste electrical and electronic equipment (WEEE) devices, waste components, and wastes from their treatment.
Guidance for designated collection facilities (DCF) and charities on how to comply with WEEE and waste regulations.
Information and guidance on a range of medical devices for users and patients.
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