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Register to vote Register by 18 June to vote in the General Election on 4 July.
Search reports on business payment practices: when invoices are paid, payment terms and practices
Information on how the CMA investigated the merger, and how you can find out more.
British travellers to the US must register with the Electronic System for Travel Authorisation (ESTA) before their journey
Official information British people moving to and living in the United States of America (USA) need to know, including residency, healthcare and driving.
Submission dates and how the submissions using the EC decision reliance procedure work.
Order birth, adoption, marriage, civil partnership and death certificates from the General Register Office (GRO) - find GRO index numbers
This guide sets out who has to apply for a permit, how to apply and explains the other rules covering travel to Antarctica.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
What to do if you think you are a victim of identity theft or fraud, and what signs to look out for.
How to access the historical censuses from 1841 to 1921.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Climate change is happening and is due to human activities; along with warming, many other changes are occurring such as melting polar ice, rising sea levels and more frequent floods, droughts and heatwaves.
Apply for the Registered Traveller service to get through UK border control faster and without filling in a landing card
This guidance explains what rules of origin (RoOs) are and the changes under the Developing Countries Trading Scheme (DCTS).
Submissions related to human medicines need to be submitted directly to the MHRA.
Information about incidents and outbreaks of Ebola and Marburg, both viral haemorrhagic fevers (VHF).
How to conform with the legal requirements for placing medical devices on the market.
Using an ecological momentary assessment to evaluate your digital health product.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
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