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.
Government Chemist publishes definitive approaches for the authentication of chondroitin
A form of IP that extends the protection of patented active ingredients present in pharmaceutical or plant protection products.
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.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Check the tariff classification for vitamin gummies.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
How HMRC deals with VAT repayment returns and what happens when there’s a delay in a repayment.
How to make sure an application relating to an authorisation for a veterinary medicine is complete and will pass validation.
Supporting documents containing information about the use and labelling of food supplements in England.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Use this form to provide additional information when you are making an application for a warrant to assist a person authorised by an emergency protection order.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
The process for the simultaneous review of veterinary medicine submissions by Switzerland’s Swissmedic and the UK's Veterinary Medicines Directorate.
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).