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Detailed guidance, regulations and rules
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Consultations and strategy
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How to use a factorial randomised controlled trial to evaluate your digital health product.
How to use a crossover randomised controlled trial to evaluate your digital health product.
This series brings together all statistical releases from the Participation Survey.
Find out if you’re an art market participant and need to register with HMRC under the money laundering regulations.
How to use a case-control study to evaluate your digital health product.
What users need to know to know about the Taking Part survey.
The following guidance has been jointly developed by the Heath Research Authority (HRA) and MHRA, in consultation with the Information Commissioners Office (ICO), on behalf of the UK.
The methodology underlying the Participation Survey, containing Official Statistics by the Department for Digital, Culture, Media and Sport
How investigators and sponsors should manage clinical trials during COVID-19
An epidemiological study comparing the health of those exposed to nuclear weapons tests to a group of personnel not exposed to radiation.
What you need to know about being part of the data use and productivity study.
How to use a feasibility study when planning the evaluation of your digital health product.
International co-operation for export credit financing, how UK Export Finance works with the OECD, the EU, the Paris Club and the Berne Union.
Guidance on social research ethics from the perspective of participants, outlining and identifying their ethical requirements.
This series brings together all documents relating to Taking Part
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