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Find out what makes a person an enabler of tax avoidance, and what to do about legally privileged communications.
How to define your participant criteria, find participants for research and handle incentives.
How to use a contextual inquiry when developing 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.
What you need to know about being part of the Taking Part survey.
How to use a crossover randomised controlled trial to evaluate your digital health product.
How to use a randomised controlled trial to evaluate your digital health product.
How to use a quasi-experimental study to evaluate your digital health product.
Using an ecological momentary assessment to evaluate your digital health product.
How to use an ethnographic study to evaluate your digital health product.
Find out how to complete and submit an Other Interest (OI) return using the HMRC spreadsheet or electronic flat text file.
How investigators and sponsors should manage clinical trials during COVID-19
How to manage participant data in a way that meets privacy laws.
Find a supplier who can provide user research participants to test your service with.
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