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Departments, agencies and public bodies
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
Providing your biometric information and supporting documents for visa and immigration applications within the UK; UKVCAS service point locations; cost of appointments.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
Apply for a Temporary Work – International Agreement visa if you're working under international law (including diplomatic households) - extend or switch, family members
Rules outlining the form, manner of delivery and method of authentication for documents delivered to Companies House in electronic or paper format.
Guidance on how to prove someone’s identity or give them access to your service or organisation.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
How organisations can renew or get a PSN service provision compliance certificate so they can use a current connection to provide a service to PSN customers.
How test manufacturers or distributors can apply for approval of their tests to sell on the UK market.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Apply for Temporary Admission to import goods to the UK, or move goods from Great Britain to Northern Ireland, and use them temporarily before re-exporting them.
Apply for a Temporary Work – Government Authorised Exchange (GAE) visa for work experience, training, research or fellowship - eligibility, extend or switch, family members
Find out about the different simplified declarations for imports and what you need to do to get authorisation to use them.
Get endorsement for the Global Talent visa to work in the UK as a researcher or academic leader - fellowship, UKRI endorsement, peer review.
How retained GEA licences authorise the export of certain controlled items to specified countries.
Find out about safety and security requirements that apply to goods entering and exiting the UK.
The process for the simultaneous review of veterinary drug submissions by Health Canada’s Veterinary Drugs Directorate and the UK's Veterinary Medicines Directorate.
The approach the MHRA intends to take for products approved or pending in decentralised procedure (DCP) or mutual recognition procedures (MRP).
Guidance on the 150-day assessment timeline for high-quality marketing authorisation applications including information on how to apply.
Use inward processing to delay or reduce import duties or VAT on goods that you process or repair.
How to file an update statement for an overseas entity and its beneficial owners or managing officers.
Don’t include personal or financial information like your National Insurance number or credit card details.
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