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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.
The government has pledged £750 million to ensure VCSE can continue their vital work supporting the country during the coronavirus (COVID-19) outbreak, including £200 million for the Coronavirus Community Support Fund, along with an additional £150 million from dormant bank...
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This guidance relates to Standard Essential Patents licensing.
How the MHRA makes decisions on whether a borderline product is a medical device and which risk class should apply.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Whistleblowing - what it is, who to tell, what to expect and how to complain if you're treated unfairly.
This guidance relates to Technical Standards and Standard Development Organisations to describe the typical first step in a Standard Essential Patent (SEP) journey.
Legal requirements for the sale of veterinary medicines on the internet and the VMD Accredited Internet Retailer Scheme (AIRS).
How to use a quasi-experimental study to evaluate your digital health product.
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