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Register to vote Register by 18 June to vote in the General Election on 4 July.
Apply for a public health exemption from the sunset clause.
In order to better understand the process of applying for a design, we recommend you view the design timeline.
The process for the simultaneous review of veterinary medicine submissions by New Zealand’s Ministry for Primary Industries (MPI) and the UK's Veterinary Medicines Directorate.
This guide sets out what population screening is, how it works, and its limitations.
The process for the simultaneous review of veterinary medicine submissions by Switzerland’s Swissmedic and the UK's Veterinary Medicines Directorate.
The Foreign, Commonwealth and Development Office's archive management teams.
These published standards relate to a number of KPIs in the VMD Deliverables and KPI document.
Find out about the symptoms of COVID-19, what to do if you or your child has them and when to get medical help.
Spellings of country names as recommended by the Permanent Committee on Geographical Names (PCGN).
DEO is the single biggest estates change programme within Defence, investing £5.1bn in modern, greener and more sustainable infrastructure.
Guidance for people with symptoms of a respiratory infection including COVID-19, or a positive test result for COVID-19.
The National Archives is the official archive and publisher for the UK government and for England and Wales. It is the guardian of some of our most iconic national documents, dating back over 1,000 years. The National Archives is a...
Guidance to hospital blood banks (HBBs) on flexible approaches to requirements
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
A competition to award funding aimed at accelerating innovation within the legal services sector and the growth of lawtech in the UK.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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