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What the retirement of analogue phone lines, also known as the Public Switched Telephone Network (PSTN), means for you.
Guidance for businesses.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How to assess and report B2C and B2B electrical and electronic equipment (EEE) and waste electrical and electronic equipment (WEEE) products.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
Information about the EU Regulations and their implementation in Northern Ireland
Get help to classify various types of vehicles such as mobility scooters, dumpers and utility vehicles, all-terrain vehicles and e-bikes for import and export.
The rules for manufacturing mercury added products in Great Britain, as well as importing and exporting them between Great Britain and non-EU countries.
Advice for manufacturers of Class I medical devices for placing products on the UK market
Information and guidance on a range of medical devices for users and patients.
Find out about which goods and services for disabled people and people aged 60 or over that you should apply zero or reduced rate VAT.
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.
Get help to classify electric lamps for import and export.
Guidance for local authorities, trusts, schools, colleges and FE institutions about who owns DfE loaned devices, asset management and loan agreements.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
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