GAERS stands for the **Global Adverse Event Reporting System**. It is a system used to collect and analyze data on adverse events related to medical products, including drugs and vaccines. GAERS is designed to improve patient safety by identifying potential safety issues, monitoring product safety, and facilitating regulatory compliance. It aggregates reports from various sources, including healthcare professionals, patients, and manufacturers, and helps regulatory authorities assess the safety and efficacy of medical products in real-time.
New to topics? Read the docs here!