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
This document details monthly management information on staff numbers and paybill costs within HM Treasury and its agencies.
Using metadata to make it easier to catalogue, validate, reuse and share your data.
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
If you hold certain information, you should contact OFSI as soon as practicable.
FCDO travel advice for Brazil. Includes safety and security, insurance, entry requirements and legal differences.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Find out what information you need to send HMRC before you make a claim for R&D Corporation Tax relief.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Find out what information accountable persons must provide to different individuals and organisations and when to transfer it.
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 and requires JavaScript).