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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.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
What you need to do to work and operate in the aviation industry.
You must tell DVLA if you have a brain abscess, cyst or encephalitis - download the correct form to let them know
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Use supplementary pages SA109 to record your residence and domicile status on your SA100 Tax Return.
Find out the rules from 1 January 2018 if you promote or use arrangements that are meant to give someone a VAT or other indirect tax saving or a tax deferral.
Find out how the new Customs Declaration Service cash account works, when it can be used and what type of customs charges you can pay.
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
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Find out how to check your risk of being involved in tax avoidance if you work through an umbrella company.
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
Guidance on how to prove someone’s identity or give them access to your service or organisation.
How to use A/B testing to evaluate your digital health product.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
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