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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
Three research reports about the value of data use to organisations, the economy and society.
How to use an ethnographic study to evaluate your digital health product.
Event data from Phases I, II and III of the government’s Events Research Programme.
This collection brings together all documents relating to DWP communications and customer insight research.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
This is a report of all the activities for Phase 2 of this project
This collection brings together all documents in the Employment Relations Research Series.
Guidance on how to report a security vulnerability on any Department for Business and Trade (DBT) IT service or system.
This collection brings together all documents relating to BIS research papers.
Barriers include stigma around TB transmission, lack of access to reliable information and limited support from editors for health stories
Research undertaken by the Research Information Network on behalf of the International Network for the Availability of Scientific Publications
Areas of research interest (ARI) give details about the main research questions facing government departments.
Field inspection reports for the Genetic Modification Inspectorate deliberate release inspection programme in England.
How to use a patient-reported outcomes and experiences study to evaluate your digital health product.
Ofsted carries out research alongside its main inspection programme to look at specific issues, subjects or policies in more detail.
How to use a cost benefit analysis to evaluate your digital health product.
Data on the real-world efficacy of the COVID-19 vaccines.
Guidance and regulatory advice on how to apply for licences issued under ASPA and how your compliance with ASPA and your licence conditions will be assessed.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
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