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.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
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.
Find out the rules to establish the country of origin of imported and exported goods and to help identify goods which qualify for lower or no Customs Duty.
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.
Check the tariff classification for a vlogging kit with ring light made of plastics.
How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
Check what you need to do to sell cosmetic products in Great Britain.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Organisational definitions of terms concerned with risk and risk-related matters.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Find out the information you must give to customers on food products and how to give it.
Get help to classify plastics for import and export.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
This guidance outlines the requirements for claiming preferential tariffs under the Developing Countries Trading Scheme (DCTS).
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
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.
Find out what a composite food product is, and the rules you need to follow to export or move these products from Great Britain to the EU and Northern Ireland.
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
This guidance provides an introductory guide to the standards and regulatory requirements that businesses may need to meet, to import and sell goods in the UK.
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).