Time to Embrace The Digital CPV


Stop losing batches, eliminate manual errors, forget about drafting CPV reports

Automate data acquisition, monitor trends in real time, and respond to deviations proactively.

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Redefining CPV for Modern Pharma

Continued Process Verification should keep quality on track, yet spreadsheets, paper logs and disconnected systems leave teams chasing data after the fact. When trends are spotted too late, batches - and revenue - are lost.

The ValGenesis Process Lifecycle Suite changes that. It digitalises CPV end‑to‑end - automating data capture, validation, analysis and report compilation. With real‑time visibility and predictive insight, you can intervene before a process drifts out of control and produce audit‑ready reports at the click of a button.

With Process Lifecycle Suite, you preserve product and revenue by preventing batch failures, reduce manual effort and free experts to focus on process optimization, and demonstrate control instantly to auditors and regulators with automatically generated CPV evidence.

Monitoring becomes continuous. Compliance becomes automatic. And batch integrity is protected at every stage.

 

This is how the Process Lifecycle Suite safeguards your batches:

  • Real time monitoring & intelligent alerts – know the moment a CPP or CQA drifts so you can act before product is at risk.
  • Predictive analytics – detect emerging patterns early and adjust processes before deviations snowball.
  • End to end report automation – from raw data capture to validated CPV reports, eliminate manual collation and accelerate QA review and release.
  • Built in compliance –controlled access and full audit trails baked in.
  • Central knowledge base – unify global sites and feed historical data back into continuous improvement.