Time to Re-Invent Pharma Validation

One connected suite. End-to-end process validation in pharma.

ValGenesis Validation Lifecycle Suite connects iVal, iClean, and iOps in a single digital platform—standardizing validation, accelerating time to market, and ensuring audit readiness across the enterprise.

Pharma Validation, Reinvented With Intelligent Automation

Validation shouldn’t feel like a fragmented mess of spreadsheets, disconnected tools, and manual tasks. The ValGenesis Validation Lifecycle Suite unifies your entire CQV, CSV, and CSA lifecycle in a centralized, standardized platform. With embedded AI, automated traceability, and seamless system integration, you’ll experience fewer errors, faster validation cycles, and continuous audit readiness.

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Replace outdated, paper-based processes and siloed systems with smarter, automated workflows designed for continuous compliance. Secure, real-time validation records, integrated impact assessments, and streamlined change management ensure your teams are always audit-ready.

No more silos. No more delays. Just smart, connected compliance - at scale.

Here’s how the ValGenesis Validation Lifecycle Suite supports pharma validation:

  • Digitalizes every phase—from protocol creation to execution, review, and audit.
  • Uses AI to flag anomalies and generate validation documents.
  • Enables risk-based validation with integrated assessments and decision trees.
  • Tracks cleaning, operations, and calibration logs in a centralized, searchable format.
  • Flags deviations, automates audit trails, and enforces SOPs with smart workflows.
  • Supports PPQ, CQV, and continuous process validation in pharma.
  • Integrates with ERP, QMS, LIMS, and MES for data continuity.
  • Cuts validation cycle time by up to 80% and boosts team productivity.
  • Standardizes validation globally with built-in regulatory alignment.