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
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Labelling rules for businesses in Great Britain (England, Scotland and Wales) and retailers in Northern Ireland, for certain agri-food products moved under the Northern Ireland Retail Movement Scheme.
Information on trade sanctions, arms embargoes and trade restrictions, including trade controls, transit controls and restrictions on terrorist organisations.
Get help to classify articles of leather and other items in chapter 42 of the tariff for import and export.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
When and how you need to register your item or apply for an exemption certificate to deal in ivory.
Get help to classify various types of vehicles such as mobility scooters, dumpers and utility vehicles, all-terrain vehicles and e-bikes for import and export.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to begin with evaluating a digital health product, including when to evaluate, budgeting and getting support.
This guidance is designed to help UKHSA customers and partners to navigate engaging and working with us and to signpost upcoming events and opportunities.
Get help to classify various items of iron and steel, primarily those classified under chapter 72.
Find out when it's possible to get zero-rated supplies on medical and research goods and services that have been funded by charities.
Find a BFPO number, send mail to and from British forces personnel and their families
We advance prosperity by ensuring no viable UK export fails for lack of finance or insurance, doing that sustainably and at no net cost to the taxpayer.
Business potential of producing crops for non-food markets, how and where to grow them and details of organisations providing grants.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Guidance for businesses trading in timber and timber-related products.
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).