The Food and Drug Administration (FDA) is the Federal agency responsible for protecting public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nation’s food supply, cosmetics, and products that emit radiation. Document Archiving, Reporting, and Regulatory Tracking System (DARRTS) is a component-based, multi-tier enterprise application that is accessed via a web-based interface. The purpose of the task order is to provide the FDA with modifications to the DARRTS Program to provide better knowledge management and analysis of data through custom templates, modules, and data analysis tools. The system runs within the Center for Drug Evaluation and Research (CDER) intranet network and is only available to authorized users. DARRTS provides FDA users with the ability to receive, manage, track, and report on drug applications.