Webinar
Avoid CPV Failures: Proven Ways to Catch Deviations Early
Discover how modern CPV strategies can transform compliance from reactive reviews into a proactive, real-time early-warning system that safeguards quality and minimizes risk.
In its 2011 Guidance for Industry: Process Validation—General Principles and Practices, the FDA formally incorporated Continued Process Verification (CPV) as the third stage of process validation. Since then, pharmaceutical companies have adopted CPV in their quality management systems to ensure consistent process performance and confirm that control strategies deliver products of the desired quality.
However, traditional CPV systems often fall short — missing early signals of deviation and exposing operations to costly consequences. This webinar explores the hidden pitfalls of legacy CPV approaches and helps you uncover operational and compliance risks tied to fragmented data systems, time-consuming manual reviews, and delayed analytics that contribute to late detection of abnormal process behaviours.
You’ll also gain insights into modern strategies for proactive monitoring, including how to implement real-time oversight, leverage multivariate analytics, and configure automated alerts. With these approaches, you will learn how to transform CPV into a proactive, action-oriented, early-warning system.
Register now to learn practical strategies for turning CPV into a proactive monitoring system that prevents costly deviations and strengthens compliance.