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.
Things to consider when buying and using products.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Find out when you can zero rate books and other forms of printed matter.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
How to use Union Transit to move non-EU goods within the UK or EU, and to move goods to or from the special territories.
How to use a before-and-after study to evaluate your digital health product.
How to apply for simultaneous review of veterinary medicine submissions to the Australian Pesticides and Veterinary Medicines Authority (APVMA) and the VMD.
Information about the EU Regulations and their implementation in Northern Ireland
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
The DUCR and the optional Part suffix is the main reference key to any Customs Handling of Import & Export Freight (CHIEF) declaration.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Submission dates and how the submissions using the EC decision reliance procedure work.
When applying to register a trade mark, you must use the classification system to specify the goods and/or services you'll be using it on.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
You can only import certain goods using an ATA Carnet to claim relief under temporary admission in the UK. Some goods have special conditions attached.
Guidance for manufacturers, importers and distributors.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
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).