Securing pharmaceutical document systems: Requirements for document approval systems in the pharmaceutical industry

In this episode, we explore the essential requirements for document approval systems in the pharmaceutical industry. Learn why software validation is critical for ensuring compliance, data integrity, and patient safety. We break down key regulatory frameworks (FDA, EMA, GxP), best practices for risk-based validation, and the vital steps pharma teams must take to stay audit-ready and efficient. Tune in to stay ahead of the compliance curve!