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This page links to Governments border related Application Programming Interfaces (APIs) which allow industry to integrate their technology with Government systems. This page will be continuously updated as APIs change and ne…
Find out how to get a legally binding decision on the commodity code to use when importing into or exporting from Northern Ireland or the EU.
How to use Method 2 to work out the customs value of your imported goods if you’re an importer or clearing agent.
Overview of insolvency and liquidation proceedings and the documents you must send to Companies House.
Find a list of codes which may be used in Data Element 5/23 to identify the location where the goods may be examined for airports (Appendix 16A).
Guidance for Official Veterinarians (OVs) and Food Competent Certifying Officers (FCCOs) on registering for EHC Online and certifying export health certificates.
Find out when Aggregates Levy applies to extracted rock, sand and gravel and when you need to register and pay.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Form A is used to give proof of origin for goods being imported from countries covered by the Developing Countries Trading Scheme.
Find out about our General Export Facility: its benefits, eligibility criteria and how to apply.
How to use the simplified declaration procedure when importing goods into the UK.
Verify or change the email address we use for your customs messages and notifications.
Guidance for manufacturers, importers and distributors on the Product Security and Telecommunications Infrastructure Act 2022 and Regulations 2023.
Training to help SME business leaders to increase productivity, seize investment opportunities and grow their business.
The date of grant and date of publication will be available online for all UK national registered designs.
Technical information about the import requirements for POAO for human consumption, for use by vets, importers and border officials.
Rules for how cases are handled in the General Regulatory Chamber, which deals with appeals against government regulators.
Information on the new regulations for the post-market surveillance of medical devices which come into effect on 16 June 2025.
Get help to classify footwear and parts of footwear for import and export.
Guidance for business and government departments.
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