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How investigators and sponsors should manage clinical trials during COVID-19
Urgent and clinically significant safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised in the UK.
Guidance on labelling for medicinal products used in clinical trials.
Information on applying for New Active Substance Work Sharing Initiative (NASWSI) and Biosimilar Work Sharing Initiative (BSWSI) assessments and list of approved products.
Guidance on using non-investigational medicinal products in a clinical trial.
A form of IP that extends the protection of patented active ingredients present in pharmaceutical or plant protection products.
Protected wine name with Protected Designation of Origin (PDO)
Criteria applied by the VMD for accepting and agreeing the invented name of veterinary medicinal products.
Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
Qualified Persons (QPs) should follow the below guidance on the flexible approaches we are taking for medicines imported from third countries.
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