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.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
The actions to take for sourcing medicines in different circumstances.
How to market forest reproductive material (FRM) for forestry purposes, including regulations, registration, master certificates and licences.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
Sources of advice and financial support for UK farmers exporting agricultural products to the EU and beyond
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
There are changes to the legislation of Reference Medicinal Products (RMPs) used to support abridged marketing authorisation applications
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.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Guidance on the European Union regulation on explosives precursors, including licensing, labelling and reporting suspicious activity
Check which supplies of sport, physical recreation, and physical education services qualify for exemption from VAT.
Lists for local authorities.
Industry must notify the MHRA if they will not be using these flexibilities
Marketing standards for poultry meat producers, manufacturers, retailers and distributors.
Rules on labelling food, feed and seed as organic or using organic production terms if you produce, prepare, store, import, export or sell organic food in the UK.
Detailed guidance on advertising and promoting medicines.
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).