Should You Digitalize Your CQV Process?

Equipment validation is too critical to stay manual.

The risk, cost, and time waste are real. 

Manual CQV processes create bottlenecks at every turn—from commissioning delays to repeated testing cycles. Paper-based equipment validation may feel familiar, but in today's high-stakes pharma and biotech environments, it's inefficient and risky.

Digital Commissioning, Qualification and Validation captures data and objective evidence in real time to ensure compliance with 21 CFR Part 11 guidelines and supports fast, traceable validation.

Digital CQV enables “right-first-time” validation through automation, standardization, and full traceability—reducing cycle times, error rates, and effort across processes involving equipment’s for validation in pharma and biotech industry.

 

The question isn’t if you should go digital.

It’s why haven’t you already?

Say Goodbye to Manual CQV Bottlenecks

Generate validation plans automatically

Ensure timely planning and documentation

Leverage the power of automated test scripts

Keep your validation documents audit-ready

Learn More About Digital CQV

Blog Post
From Weeks to Minutes: How Intelligent Automation Transforms CQV Workflows

Discover how intelligent automation transforms CQV workflows and streamlines equipment qualification in pharma—cutting costs, time, and risk.

Read the Blog Post
Webinar
Digital CQV and Pharma 4.0: Paving the Way for Future Success

Watch the Webinar
Webinar
CQV: From a Painful Manual Approach to a Smooth Digital Process

Transform your CQV process with ValGenesis VLMS: a seamless digital solution to eliminate manual pain points and streamline your transition to a fully digital environment.

Watch the Webinar

Talk to us to see how ValGenesis can digitalize your CQV process.