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
Running a limited company - including directors' responsibilities, company annual returns, reporting company changes and how to take money out of a limited company
Marking, labelling and marketing standards you must follow to import and export plant seeds, food and manufactured goods.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Practice note on how immigration advice and services might be promoted to potential clients.
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.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Check which supplies of sport, physical recreation, and physical education services qualify for exemption from VAT.
How VAT applies if you give or get sponsorship.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
There are changes to the legislation of Reference Medicinal Products (RMPs) used to support abridged marketing authorisation applications
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
This guidance sets out how the MHRA is handling centralised applications that were still pending on 1 January 2021.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
Marketing standards for hops producers, manufacturers, retailers and distributors.
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).