LinkedIn·Tuesday, 7 July 2026·07 Jul 2026
Continuous Process Verification is mandatory — and for many teams it is one of the most resource-intensive activities they run: often…
DNAlytics
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Continuous Process Verification is mandatory — and for many teams it is one of the most resource-intensive activities they run: often manual, and limited in the number of parameters it can realistically cover.
At A3P Belgique a few weeks ago, our colleague Marie Bastin made the case for turning CPV from a regulatory hurdle into a source of value.
The shift is twofold.
1️⃣ Automation: what takes weeks of manual work, such as control charts, capability indices, trend and normality checks across dozens of parameters, can run continuously and produce review-ready reports in minutes, with full traceability.
2️⃣ Even more important: the effort you invest in structuring your data for CPV doesn't only serve CPV. It creates a reusable data foundation, separating the representation of your process (built on the ISA-88 standard) from the observations, that powers everything downstream, from deviation investigations to process improvement.
🎁 In other words: the compliance work you already have to do can become the data asset your process knowledge is built on.
Thanks to Marie for a great talk, and to A3P Association for the platform.
Curious how others are approaching CPV automation and always happy to exchange.
#CPV #QualityByDesign #Biomanufacturing #GMP #A3P
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