Operational Readiness in Pharma
Operational readiness is the critical bridge between project delivery and reliable GMP manufacturing — and for pharmaceutical and biotech organizations, getting it right means the difference between a smooth facility start-up and costly delays. In this on-demand webinar, PM Group's Michael Sweeney, EVAL Electronic Lead, and Fintan Coady, Senior CQV and Operational Readiness Specialist with over 20 years of pharmaceutical and biologics manufacturing experience, explore how digital validation strengthens operational readiness across the entire project lifecycle. Drawing on deep expertise in commissioning, qualification, and validation (CQV) and GxP compliance, they show how Kneat Gx enables pharma and biotech teams to accelerate technology transfers, enable real-time project tracking, automate change control, streamline risk assessments, and maintain continuous audit readiness from project start through facility handover. *What you'll learn:* How digital validation accelerates pharmaceutical technology transfers and facility start-ups How to enable real-time project tracking across CQV programs with Kneat Gx How to automate change control and streamline risk assessment in GxP environments How to maintain continuous GMP compliance and audit readiness throughout your project lifecycle Watch now and build a stronger operational readiness program.

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