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Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
This guidance relates to Standard Essential Patents licensing.
This is a check-against-delivery text of the speech 'Discourse: The future of engineering biology' delivered by Government Chief Scientific Adviser Professor Dame Angela McLean at The Royal Institution on 25 April 2025.
How the MHRA makes decisions on whether a borderline product is a medical device and which risk class should apply.
This guidance relates to Technical Standards and Standard Development Organisations to describe the typical first step in a Standard Essential Patent (SEP) journey.
Whistleblowing - what it is, who to tell, what to expect and how to complain if you're treated unfairly
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to use a quasi-experimental study to evaluate your digital health product.
Legal requirements for the sale of veterinary medicines on the internet and the VMD Accredited Internet Retailer Scheme (AIRS).
How to use an interrupted time series to evaluate your digital health product.
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