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Data First is a pioneering data-linking, research and academic engagement programme led by the Ministry of Justice and funded by ADR UK.
Guidance for those conducting research and development on genetic resources.
Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
This section of the SEPs Resource Hub provides an explanation of SEP specific words and terms used throughout the guidance.
This guidance relates to Technical Standards and Standard Development Organisations to describe the typical first step in a Standard Essential Patent (SEP) journey.
This series brings together all documents relating to Allied Joint Publications.
Details of the exceptions to copyright that allow limited use of copyright works without the permission of the copyright owner.
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.
Find out about gaining approval for a fair partial exemption special method if you deal with partial exemption for insurers.
Protection in the EU for databases produced in the UK.
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