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How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.
Ensuring the seasonal flu vaccine is ready, safe and effective involves months of international planning, testing and collaboration
A proactive, collaborative, agile and the first of its kind approach to identifying and addressing the challenges faced by AI as a Medical Device (AIaMD).
Up to £55 million is available through the second phase of the RD&D programme to support the development and demonstration of High Temperature Gas Reactor (HTGR) technology in the UK.
An overview of the recyclability assessment methodology (RAM). Under extended producer responsibility for packaging, large producers must report the recyclability of some packaging materials
Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
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