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
Campaign highlights how a simple CLICK can save lives.
At DASA, we find and fund exploitable innovation to support UK defence and security quickly and effectively, and support UK prosperity.
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
Submission dates and how the submissions using the EC decision reliance procedure work.
Statistical notice about a change to the next release of income-related benefits: estimates of take-up official statistics.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
A list of upcoming webinars on the UK’s approach to product marking and placing products on the market in Great Britain and Northern Ireland.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Ordinary people mistreated or wronged by big, powerful companies will have a better chance of bringing them to court to access justice, thanks to plans unveiled today (4 March 2024).
Find out how to prove the originating status of your goods and check if you can claim preferential tariff treatment.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Information about the EU Regulations and their implementation in Northern Ireland
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Blogs where government organisations talk about their work and share information and ideas.
This sets out the decision-making process for selecting successful bids to Round 3 of the Levelling Up Fund.
Special feature articles on energy issues in the United Kingdom from the quarterly statistical bulletin Energy Trends.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
FCDO travel advice for the Dominican Republic. Includes safety and security, insurance, entry requirements and legal differences.
How investigators and sponsors should manage clinical trials during COVID-19
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).