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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
What private maritime security companies (PMSCs) with a trade control licence must do when their circumstances change like leaving the sector or merging.
How employees, employers and their representatives can resolve disputes about setting up and running a European Works Council (EWC) under the Transnational Information and Consultation of Employees Regulations (TICER).
Foresight projects give evidence to policymakers to help them create policies that are more resilient to the future.
How to find and use the statistics and analysis from the People and Nature Surveys for England.
How to use a cost effectiveness analysis to evaluate your digital health product.
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
This series brings together all documents relating to Taking Part
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 use feedback from marketplace reviews to evaluate your digital health product.
Helping public health practitioners conducting evaluations – using economic evaluation to identify the value gained from an intervention.
Information on the programme, including the screening tests, commissioning, quality assurance, education and training.
What to do if you think you are a victim of identity theft or fraud, and what signs to look out for.
Guidance for commissioners and health professionals to make decisions about mental health services and interventions based on data and analysis.
This Privacy Notice explains who is processing your data, the personal data we collect, how we use it, who we share it with, and what your legal rights are.
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.
Report your missing or lost dog to the council's dog warden service
We support exporters and project developers in receipt of UK exports to manage project-related environmental, social and human rights risks and impacts.
How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.
How investigators and sponsors should manage clinical trials during COVID-19
This information is provided to help British nationals make decisions about getting medical advice and reporting a rape or sexual assault in Russia.
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