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Keywords

Argus Safety Database, pharmacovigilance, drug safety, adverse event management, regulatory compliance

Abstract

The Argus Safety Database is a comprehensive pharmacovigilance solution designed to manage drug safety data and ensure compliance with global regulatory requirements. In today’s complex pharmaceutical landscape, the management of adverse event (AE) data has become critical for drug safety surveillance. Argus Safety provides an all-encompassing platform that supports case processing, signal detection, medical coding, and automated regulatory reporting. This review article delves into the key features, architecture, and functionality of the Argus Safety Database, exploring its significant role in both pre-marketing and post-marketing drug safety. Additionally, the article evaluates the software's strengths, limitations, and its comparative advantage over other pharmacovigilance systems. Finally, it provides insights into future advancements, such as artificial intelligence (AI) integration and real-time analytics, which are likely to shape the next generation of drug safety systems. The review concludes with a detailed analysis of how Argus Safety contributes to improved patient outcomes, efficient regulatory compliance, and more proactive pharmacovigilance efforts.

  
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