Continued Process Verification (CPV) was introduced with the FDA’s 2011 Process Validation guidance as the third stage of process validation ― designed to ensure consistent quality, performance, and control strategy effectiveness across the product lifecycle. 

CPV was never intended to consume subject matter expert (SME) time. However, for many life sciences organizations, it has quietly become a significant high-effort, low-value activity driven by fragmented systems, disconnected spreadsheets, and repetitive manual reporting. 

Manual CPV doesn’t just slow teams down; it diverts SMEs from true quality oversight. Disparate data sources and delayed trend reviews force organizations into reactive decision-making, often after issues have already escalated. 

Instead of enabling early signal detection and continuous improvement, manual CPV limits quality experts’ ability to act with confidence and control. 

In this webinar, you’ll see how ValGenesis iCPV™ transforms CPV from a manual data-handling burden into a continuous, standardized, inspection-ready quality capability ― without disrupting existing operations. 

The result: faster, more confident decisions, stronger data integrity, audit readiness by default, and teams freed to focus on what matters most ― product quality and continuous improvement. 

Register for this webinar to learn how to: 

• Eliminate manual CPV tasks such as data extraction, spreadsheet compilation, and chart creation. 

• Improve data integrity and audit readiness with automated, standardized CPV workflows. 

• Replace delayed, retrospective CPV reports with automated trend detection. 

• Respond faster to process signals with actionable, real-time insights. 

• Modernize CPV without disrupting your current operations.