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What you need to know about being part of the Taking Part survey.
How to complete and submit an Other Interest (OI) return using the HMRC spreadsheet or electronic flat text file.
Find out what makes a person an enabler of tax avoidance, and what to do about legally privileged communications.
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 the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
How to use a quasi-experimental study to evaluate your digital health product.
How to use a randomised controlled trial to evaluate your digital health product.
How to define your participant criteria, find participants for research and handle incentives.
Find a supplier who can provide user research participants to test your service with.
How investigators and sponsors should manage clinical trials during COVID-19
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