The Triage Process in Pharmacovigilance plays a critical role in managing adverse event reports efficiently. It evaluates key factors such as the validity of the case report, the seriousness of the adverse event, and whether the event is labeled or unlabeled. This systematic approach ensures accurate prioritization and timely processing of cases, supporting effective pharmacovigilance practices. By identifying serious and unlabeled events quickly, it helps healthcare professionals focus on critical safety concerns, ensuring patient safety and regulatory compliance. The Triage Process tool simplifies adverse event management, providing a reliable framework for assessing and categorizing reports in a structured manner.