Developing Your Risk-Based Approach To Single-Use System Integrity

Single-use systems (SUS) have become a cornerstone of biopharmaceutical manufacturing, but ensuring their integrity remains a dynamic challenge. As regulatory expectations evolve, manufacturers must adopt a more comprehensive approach to contamination control. This webinar explores the full lifecycle of SUS, emphasizing the importance of clear user requirement specifications (URS) and a holistic strategy for system integrity. Gain insights into aligning operational efficiency with compliance, and learn how to build a robust contamination control framework that stands up to regulatory scrutiny. Whether you're refining an existing strategy or starting from scratch, see how you can help safeguard product quality and streamline operations.