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Register to vote Register by 18 June to vote in the General Election on 4 July.
Check the tariff classification for accessories for toys.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
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.
How to get fast-track approval of medical devices during COVID-19.
List of manufacturers and their medical devices granted an exemption by MHRA. The list also includes manufacturers whose exemption expired or was cancelled.
Service providers or government departments installing networking technologies in government shared buildings, known as hub buildings.
Find out about the calculation of the company car benefit charge.
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 about the EU Regulations and their implementation in 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.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Guidance for manufacturers, importers and distributors.
Get help to classify articles of leather and other items in chapter 42 of the tariff for import and export.
Advice for manufacturers of Class I medical devices for placing products on the UK market
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Get help to classify drones and aircraft parts for import and export.
Information and guidance on a range of medical devices for users and patients.
Information on road traffic devices, such as breath-testing, speed cameras and immobilisation devices.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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