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How to use feedback from marketplace reviews to evaluate your digital health product.
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.
How to use a behaviour change techniques review to evaluate your digital health product.
How to use an interrupted time series to evaluate your digital health product.
Things to consider when buying and using products.
Guidance on choosing evaluation study types and methods.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Domestic homicide review online learning for frontline practitioners.
This research from 2014 compares the pros and cons of using item-level marking in exams rather than whole-script marking.
How to use an ethnographic study to evaluate your digital health product.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to use a quasi-experimental study to evaluate your digital health product.
How to create a model of how your digital health product works and choose measures for your evaluation.
The rules about product labelling - including special rules for retailers and manufacturers in different business sectors (like food, jewellery and toys)
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
Extradition processes and agreements between the UK and other countries, role of the Secretary of State, High Court and Supreme Court.
An independent review of the UK's system for the recall of unsafe products.
How a marketing authorisation holder should report a defect with a veterinary medicine.
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