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How to use an interrupted time series to evaluate your digital health product.
How investigators and sponsors should manage clinical trials during COVID-19
These principles describe how the government should manage legacy technology.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
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This plan explains how the Department for Culture, Media and Sport will implement the Charities Act 2022.
Information about the MHRA regulates medical devices in Northern Ireland and what legislation applies to manufacturers and suppliers.
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