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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 to comply with the regulatory requirements for manufacturing custom-made medical devices.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Get help to classify textiles and which headings and codes to use.
Self-build and custom housebuilding registers.
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
Find out about the different simplified declarations for imports and what you need to do to get authorisation to use them.
Get help to classify articles of leather and other items in chapter 42 of the tariff for import and export.
Get help to classify ceramic articles for import and export.
Find out how to prove the originating status of your goods and check if you can claim preferential tariff treatment.
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.
Find out about the different types of delivery costs, and which ones you must include or exclude in the customs value if you’re an importer or clearing agent.
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