What Does AERS Stand For?

AERS stands for Adverse Event Reporting System

The Adverse Event Reporting System (AERS) is a comprehensive framework designed to collect, analyze, and manage reports of adverse events related to pharmaceutical products and medical devices. AERS plays a crucial role in enhancing patient safety by identifying potential safety signals, monitoring trends in adverse events, and facilitating regulatory decision-making. It serves as a vital tool for healthcare professionals, manufacturers, and regulatory authorities to ensure the efficacy and safety of medical products throughout their lifecycle.