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.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
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.
Supporting documents containing information about the use and labelling of food supplements in England.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
A form of IP that extends the protection of patented active ingredients present in pharmaceutical or plant protection products.
How the MHRA makes decisions on what is a medicinal product (borderline products).
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
Get help to classify organic chemicals that contain certain permitted additives or can be dissolved in water, for import and export.
How HMRC deals with VAT repayment returns and what happens when there’s a delay in a repayment.
Check the tariff classification for vitamin gummies.
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.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
Food and drink labelling and packaging regulations - what you must show, warnings, health and organic labels and packaging standards.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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).