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How to use a cost utility analysis to evaluate your digital health product.
How to use a quasi-experimental study to evaluate your digital health product.
How to use a before-and-after study to evaluate your digital health product.
Using an ecological momentary assessment to evaluate your digital health product.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
Common user charge rates and how the charge applies to imports entering Great Britain through the Port of Dover and Eurotunnel.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Get help to classify plastics for import and export.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
How to use a randomised controlled trial to evaluate your digital health product.
How to get fast-track approval of medical devices during COVID-19.
Design, build and operate APIs in a consistent way
Get help to classify various items of iron and steel, primarily those classified under chapter 72.
How to use a crossover randomised controlled trial to evaluate your digital health product.
Information on depleted uranium (DU) including what it is, its uses, health effects and protection from exposure.
How data on landings statistics are collected and processed by fisheries administrations in the UK.
The UK government's design principles and examples of how they've been used.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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