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.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Submissions related to human medicines need to be submitted directly to the MHRA.
How to submit a proposal to the Defence and Security Accelerator
Submission dates and how the submissions using the EC decision reliance procedure work.
What detailed information you need to send to HMRC to support your Research and Development (R&D) tax relief claim, and when and how to submit it.
Submit new evidence if your asylum application has been refused and you have no more right to appeal - called ‘further submission’
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Make building control applications to any local authority in England, Wales or Northern Ireland.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to apply for marketing authorisation via this new procedure.
How to renew marketing authorisations for products granted through different routes and at different times.
Upper Tribunal Administrative Appeals Chamber decision by Judge Brunner on 3 May 2024.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
The process for applicants applying for a Paediatric Investigation Plan (PIP) modification or waiver.
Guide to submitting research applications to the Administration of Radioactive Substances Advisory Committee (ARSAC).
Find out how to submit your research to Athena, Dstl's central repository of MOD-sponsored scientific and technical research reports.
Guidance for local authorities, port health authorities and food traders on how to submit a sample for referee analysis.
If you're moving goods outside the UK, you'll need to make an exit summary declaration if you've not fulfilled safety and security requirements with a full customs export declaration.
How to submit an application, data package and responses for proposed or existing marketing authorisations.
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).