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Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
How to get information including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
Find software developers that can help with entry summary declarations including safety and security declarations for imports.
Formerly part of M18, technical guidance for industrial plant operators (and their contractors) who monitor effluent discharges to water and sewer.
Employment Appeal Tribunal Judgment of Michael Ford, Deputy Judge of the High Court on 19 December 2025.
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