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VisitBritain (VB) is the national tourism agency, responsible for marketing Britain worldwide and developing Britain’s visitor economy. It works with UK Trade & Investment as well as airlines, travel operators, global brands and the official tourism bodies for London, England,...
Pharmacovigilance system requirements
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.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Countries have their own rules about what goods you can bring in using an ATA Carnet. Check with the issuer in the country you’re exporting to.
The Civil Aviation Authority (CAA) is responsible for the regulation of aviation safety in the UK, determining policy for the use of airspace, the economic regulation of Heathrow, Gatwick and Stansted airports, the licensing and financial fitness of airlines and...
Reclaim VAT you've paid on goods and services bought in the UK to use in your business if you’re registered as a business outside the UK.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
What you need to do to work and operate in the aviation industry.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
Nigeria is subject to regional controls governing small arms and light weapons.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Find out about Import VAT and Customs Duty when you send gifts into the UK.
Putting your goods into temporary storage means you can delay the full customs declaration and payment of import VAT and duty for up to 90 days.
Work out the VAT liability of goods and services supplied by health and care institutions and providers of non residential care to children.
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
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
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