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Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to approach sampling ambient air and the sampling and analytical techniques to use.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to use an interrupted time series to evaluate your digital health product.
How to use a behaviour change techniques review to evaluate your digital health product.
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How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
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