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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.
Whistleblowing - what it is, who to tell, what to expect and how to complain if you're treated unfairly
You’re a whistleblower if you’re a worker and you report certain types of…
You can tell your employer - they may have a whistleblowing policy that…
You can take a case to an employment tribunal if you’ve been treated…
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.
This guidance relates to Technical Standards and Standard Development Organisations to describe the typical first step in a Standard Essential Patent (SEP) journey.
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).
This section of the SEPs Resource Hub provides an explanation of SEP specific words and terms used throughout the guidance.
Find out how to determine the place of supply of your services and how to deal with supplies of services which you receive from outside the UK.
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