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Get help to classify ceramic articles for import and export.
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.
Get help to classify footwear and parts of footwear for import and export.
The rules, paperwork and training you need to transport dangerous goods
Get help to classify various items of iron and steel, primarily those classified under chapter 72.
Documents relating to measles, mumps or rubella (MMR) oral fluid testing.
UK Health Security Agency's laboratories provide a comprehensive range of microbiological tests and services.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
Find out what the technical terms used in the scheme information for the SFI 2023 offer mean.
The epidemiology, symptoms, diagnosis and management of human T-cell lymphotropic virus types 1 and 2 (HTLV-1 and HTLV-2).
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Get help to classify various types of wood for import and export.
For waste operators and exporters classifying some waste electrical and electronic equipment (WEEE) devices, waste components, and wastes from their treatment.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
How to assess household and non-household packaging from 2024 onwards if you’re a UK organisation affected by extended producer responsibility (EPR) for packaging.
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 product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
Check the tariff classification for new pneumatic rubber tyres of a kind used on motor cars, buses or lorries, and trailers.
From 1 October 2024, more materials facilities will need to sample and report their waste. Sampling and reporting will be more detailed and more frequent under the amended regulations.
The Medicines and Healthcare products Regulatory Agency (MHRA) has today (11 March 2024) approved the medicine quizartinib (Vanflyta) to be used alongside chemotherapy as first line treatment for adults who have acute myeloid leukaemia (AML).
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