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Listing of countries with a known occurrence of high consequence infectious disease (HCID).
The Intellectual Property Office (IPO) is the official UK government body responsible for intellectual property (IP) rights including patents, designs, trade marks and copyright. IPO is an executive agency, sponsored by the Department for Science, Innovation and Technology , supported...
This guidance outlines the requirements for claiming preferential tariffs under the Developing Countries Trading Scheme (DCTS).
Advice and guidance on the health needs of migrant patients from Argentina for healthcare practitioners.
How to object to the registration of a lasting or enduring power of attorney - including forms and fees
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
We pursue our national interests and those of British citizens. We safeguard the UK’s security, defend our values, reduce poverty and tackle global challenges with our international partners. FCDO is a ministerial department, supported by 12 agencies and public bodies...
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Guidance on how to prove someone’s identity or give them access to your service or organisation.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Imposing safeguard measures for imports of certain steel products.
Check how much your visa application costs in the country you’re in
Information on embargoes on West African States and how to apply for an export licence.
The requirements for packaging DNLEU
Find out about local procedures, burials and cremations, and returning the body to the UK.
Find out what you'll need to get a legally binding decision on the commodity code to use when importing or exporting your goods.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
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