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An epidemiological study comparing the health of those exposed to nuclear weapons tests to a group of personnel not exposed to radiation.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to use a contextual inquiry when developing your digital health product.
How investigators and sponsors should manage clinical trials during COVID-19
This series brings together all documents relating to Taking Part
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
What users need to know to know about the Taking Part survey.
This page introduces the Participation Survey and links to all relevant documents.
Helping public health practitioners conducting evaluations – choosing evaluation methods.
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.
Providing vital research into COVID-19 immunity and vaccine effectiveness nationally.
How to use a think aloud study to evaluate your digital health product.
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.
Guidance on social research ethics from the perspective of participants, outlining and identifying their ethical requirements.
How to use usability testing to evaluate your digital health product.
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