Why Reviewing Labs and Adverse Events in Isolation Is a Safety Risk

Labs and adverse events (AEs) are two views of the same patient. When medical monitors, safety reviewers, or CRAs assess them through separate workflows — separate triggers, separate thresholds, separate sign-offs — the review can miss the pattern that only appears when both are read on one timeline. This briefing outlines why isolated review is […] The post Why Reviewing Labs and Adverse Events in Isolation Is a Safety Risk appeared first on Saama .