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.
UK Statements delivered on 22 and 23 May 2024 at the WTO General Council in Geneva.
Documents, certificate, letters, and notes available from the British embassy and consulates in the USA.
This guide sets out who has to apply for a permit, how to apply and explains the other rules covering travel to Antarctica.
Information about incidents and outbreaks of Ebola and Marburg, both viral haemorrhagic fevers (VHF).
Submission dates and how the submissions using the EC decision reliance procedure work.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
British travellers to the US must register with the Electronic System for Travel Authorisation (ESTA) before their journey
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Using an ecological momentary assessment to evaluate your digital health product.
Submissions related to human medicines need to be submitted directly to the MHRA.
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
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.
How to minimise your risk, and what to do if there's a terrorist attack.
Engage with the Ministry of Defence (MOD) on SKYNET Enduring Capability (SKEC), the next generation of solutions for future satellite communication programmes.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Official information British people moving to and living in the United States of America (USA) need to know, including residency, healthcare and driving.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Check if your import, export or re-export needs a permit or certificate under the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES).
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).