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Urgent and clinically significant safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised in the UK.
Explanation for animal owners and veterinary health professionals on how the VMD calculates adverse event incidence rates for veterinary medicines
Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
You can make observations on the patentability of a published patent application.
The Evidence Project Final Report is designed to capture the information on the results and outputs of Defra-funded research.
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
Guidance for organisations certified against the UK digital identity and attributes trust framework who offer delegated authority as part of their service.
Guidance on labelling for medicinal products used in clinical trials.
This guidance relates to Technical Standards and Standard Development Organisations to describe the typical first step in a Standard Essential Patent (SEP) journey.
The Company Names Tribunal practice direction provides the framework for the management of proceedings brought before the Tribunal.
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