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How to use a quasi-experimental study to evaluate your digital health product.
How the MHRA makes decisions on whether a borderline product is a medical device and which risk class should apply.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
This guidance relates to Technical Standards and Standard Development Organisations to describe the typical first step in a Standard Essential Patent (SEP) journey.
A project exploring why tax is complex and how to measure complexity
Find out if you need to follow standing advice when completing a flood risk assessment and what to do.
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