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News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
How end-use controls apply to weapons of mass destruction (WMD) related goods, software, technology and technical assistance.
How to apply for repayment of import duty and VAT on protective equipment or medical supplies brought into the UK from non-EU countries from 30 January 2020 up to 31 December 2020.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
How to apply for national listing of agricultural and vegetable plant varieties in Great Britain and Northern Ireland.
This guide gives advice about the death of a British person in the Dominican Republic, including information on burial, cremation and repatriation.
Find out about local procedures, burials and cremations, and returning the body to the UK
Information on trade sanctions, arms embargoes and trade restrictions, including trade controls, transit controls and restrictions on terrorist organisations.
How to classify and describe your business waste so you can know how to manage and dispose of it - what you need to do, List of Waste (LoW) codes, technical guidance.
The Foreign, Commonwealth & Development Office (FCDO) provides lists of English-speaking lawyers abroad to help British nationals find the legal support they need.
This guide gives advice about the death of a British person in Mexico, including information on burial, cremation and repatriation.
Learn how to check if your website or mobile app is accessible.
The seeds which must be certified before you can market them, how to get them certified and how to get a licence for your seed business.
Guidance for exporting nuclear equipment, material and technology that appears on what is known as the 'Trigger List'.
This guide gives advice about the death of a British person in Japan, including information on burial, cremation and repatriation.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
How UK organisations that supply or import packaging should comply with extended producer responsibility (EPR) for packaging.
You may need a visa to come to the UK to visit, study or work.
Apply for the Registered Traveller service to get through UK border control faster and without filling in a landing card
Advice on writing clear notices and maximising replies to your FSNs.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Don’t include personal or financial information like your National Insurance number or credit card details.
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