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Register to vote Register by 18 June to vote in the General Election on 4 July.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
We’re working to help people securely prove who they are without having to rely on physical documents.
Find out about how we manage unacceptable behaviour consistently and fairly.
The Regulatory Policy Committee provides the government with external, independent scrutiny of the evidence supporting changes in law that affect businesses, charities and community groups.
From discovery to real-world impact, VDEC equips scientists with the expertise and facilities to navigate each step in the development of vaccines and therapeutics.
Dstl ensures the UK can develop and exploit new sensor technologies for our defence and security, to find and assess potential threats and give information to decision-makers.
How schools can share daily attendance data.
The purpose of Thames Estuary 2100 (TE2100) and the challenges it aims to address.
Guidance on the national tuberculosis (TB) strain typing service, including its work, achievements, objectives, and future direction.
Learn more about the circumstances that can lead to a licence holder losing their licence, either permanently or temporarily.
A proactive, collaborative, agile and the first of its kind approach to identifying and addressing the challenges faced by AI as a Medical Device (AIaMD).
The pre-clinical evaluation team at VDEC provides a safe and controlled environment to test new vaccines and therapeutics before they progress to clinical trials
An overview of the work the IPO is undertaking in relation to Standard Essential Patents.
Advice to British people affected by crises abroad such as large-scale terrorist attacks, natural disasters and political unrest, and how the FCDO can help.
Statement by Ambassador James Kariuki at the UN Security Council meeting on the situation in the Middle East.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
This document details the service standards of the Veterinary Medicines Directorate (VMD)
Find out what unacceptable or unreasonable actions are and how we approach them.
Subject matter specialists provide invaluable advice to Ofqual as we carry out our role in regulating qualifications. Find out how to apply to be one.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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