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.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
You can claim relief to pay no Customs Duty and VAT if you're importing therapeutic substances of human origin, blood-grouping or tissue-typing reagents, or related packaging, solvents and accessories.
How to get a marketing authorisation for an Advanced Therapy Medicinal Product (ATMP) so it can be sold and/or supplied in Great Britain.
Find out which live animals and animal foods or feeding stuffs are zero-rated for VAT.
Find out how to apply VAT zero rating for the supply of those plants and seeds that are used to grow food for human consumption.
How bottled water producers can get a natural mineral water recognised in England, and rules you need to follow to produce and label it.
How to apply for a traditional herbal registration (THR) to market a herbal medicine in the UK.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
What is involved in regulatory judgements and gradings
VICH consultation until 30 November 2024 on guidelines relating to the technical requirements for demonstrating genotoxic safety of residues of veterinary drugs in human food.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Guidance on the planning for mineral extraction in plan making and the application process.
Diseases and health problems in sheep and goats, including foot and mouth disease (FMD), scrapie and lead poisoning
Guidance for prescribing vets on the use of the cascade.
An approach to payment for providers of IAPT services that links payment to patient outcomes as well as the provider’s levels of activity.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
Prescribing or supplying veterinary medicines including requirements for registration and inspection of premises.
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).