In the ever-evolving landscape of pharmaceutical manufacturing, the integration of advanced technology has become a cornerstone of ensuring product quality, patient safety, and regulatory compliance. One crucial aspect of this integration is Pharmaceutical Computer System Validation (CSV). This meticulous process holds immense significance in the pharmaceutical industry, as it ensures that computer systems utilized in various stages of drug development, production, and distribution function reliably, consistently, and in accordance with regulatory guidelines. Pharmaceutical CSV involves a series of documented procedures, testing, and assessments that establish the accuracy and reliability of computer systems used in critical pharmaceutical operations. These systems encompass a broad spectrum of functions, including manufacturing equipment, laboratory instruments, quality control processes, data management systems, and more. By validating these systems, pharmaceutical companies can mai