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
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Documents, certificate, letters, and notes available from the British embassy and consulates in the USA.
Employment Appeal Tribunal Judgment of Mrs Justice Eady on 3 May 2024.
This guidance outlines the requirements for claiming preferential tariffs under the Developing Countries Trading Scheme (DCTS).
How to use a quasi-experimental study to evaluate your digital health product.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
Get help to classify footwear and parts of footwear for import and export.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
An overview of the work the IPO is undertaking in relation to Standard Essential Patents.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to set out your charity's purposes and rules in its governing document, how to start using it and how to change it.
Find out how you could do the SFI actions for soils.
Find out about the rules for placing transportable pressure equipment on the market in Great Britain from 1 January 2023.
Project Orbis is a programme to review and approve promising cancer drugs helping patients access treatments faster.
Guidance to help you assess if artificial intelligence (AI) is the right technology for your challenge.
How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
Explanation of terms used in Ofsted's official and national statistical releases.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
A list of 10 criteria that represent good practice in creating, applying and enforcing design codes.
Get help to classify rice and related products for direct human consumption for import and export.
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.