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
VICH consultation until 15 August 2024 on guidelines relating to the technical requirements for demonstrating pharmaceutical development of veterinary medicinal products.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Information relating to rare side effects after vaccination.
Check the tariff classification for impregnated glass fibre weave articles.
Quarantine requirements for live amphibians of the order Caudata (salamanders and newts)
How test manufacturers or distributors can apply for approval of their tests to sell on the UK market.
Form to object to an application to register a traditional term for a wine product under the UK GI scheme.
Calculate nutrient budgets for developments in the catchment of Hornsea Mere SPA.
This research project aims to develop improved methods for the determination of mycotoxins.
Information for healthcare professionals and the public about the adapted Spikevax XBB.1.5 vaccine
Use this form to get your vehicle testing and calibration equipment approved by DVSA.
Application form to transfer a sealed sources radioactive substances environmental permit.
Information, resources and guidance relating to the evaluation of COVID-19 tests.
Product Safety Report for I.B.N. Steam Nail Gel Removal Machine presenting a high risk of electric shock.
The agreement between the government and the Association of British Insurers (ABI) on the use of genetic test results in underwriting insurance policies.
The Minister for the Cabinet Office has published the Terms of Reference of the Infected Blood Inquiry Response Expert Group
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
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. We’ll send you a link to a feedback form. It will take only 2 minutes to fill in. Don’t worry we won’t send you spam or share your email address with anyone.