We use some essential cookies to make this website work.
We’d like to set additional cookies to understand how you use GOV.UK, remember your settings and improve government services.
We also use cookies set by other sites to help us deliver content from their services.
You have accepted additional cookies. You can change your cookie settings at any time.
You have rejected additional cookies. You can change your cookie settings at any time.
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
Register to vote Register by 18 June to vote in the General Election on 4 July.
Information about ensuring blood and blood component safety.
The UK's regulatory framework for strategic export controls and the circumstances where you might need an export licence.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Find out how to apply for a duty deferment account, so you can delay paying most customs or tax charges when you import goods or release goods from an excise warehouse.
Guidance for holders of Marketing Authorisations approved in Northern Ireland or the EU/EEA member states who want to bring a product to market in Great Britain.
How to make an origin declaration if you're using it as proof of origin for products using the Developing Countries Trading Scheme.
Use inward processing to delay or reduce import duties or VAT on goods that you process or repair.
Find out about the VAT place of supply rules if your business sells digital services to private consumers.
How someone in Austria can get documents legalised, witnessed or certified, take an oath, affirmation or affidavit and obtain informative notes on UK naming law
Follow this guidance with help from your CDDO adviser to categorise digital and technology activity in your pipeline.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
How to use paper forms to set up agent authorisations to deal with HMRC.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
How to comply with the exemption from the Veterinary Medicines Regulations that allow certain animal medicines to be sold without a marketing authorisation.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
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.
Don’t include personal or financial information like your National Insurance number or credit card details.
To help us improve GOV.UK, we’d like to know more about your visit today. Please fill in this survey (opens in a new tab).