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How to use a randomised controlled trial to evaluate your digital health product.
This toolkit provides an outline of evidence-based antimicrobial stewardship in inpatient care settings.
A guide to collecting data about your packaging. This is for UK organisations affected by extended producer responsibility (EPR) for packaging.
Annual reports on anti-money laundering and countering the financing of terrorism.
This guidance sets out how the MHRA is handling centralised applications that were still pending on 1 January 2021.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
This series brings together all documents relating to radiological and nuclear incident monitoring.
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