UK MHRA · April 27, 2026

Clinical trials for medicines: collection, verification and reporting of safety events

Guidance on procedures for collecting, verifying and reporting safety events in investigational medicinal product trials.

High obligation Framework Clinical Trials & Research Pharmaceuticals UK Clinical trials

Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.

Read the official source ↗

Published by UK MHRA. HealthSignal links to the original document; the summary above is extracted from the source text.