9 Takeaways from ‘Repairing a C&Q Program With Digitization’
At Validate 2024 in Berlin, Pierre Winnepenninckx delivered a compelling talk titled “Repairing a C&Q Program with Digitization,” offering deep insights into how companies can
At Validate 2024 in Berlin, Pierre Winnepenninckx delivered a compelling talk titled “Repairing a C&Q Program with Digitization,” offering deep insights into how companies can
In the regulated pharma environment, “what is not documented is not done”. While many organisations in the pharma industry have been using paper to document
As previously discussed in my earlier blog post on “What is paperless validation in the pharmaceutical industry”, we looked at the driver for a paperless
Our client’s email mentioned: “As we are considering using Kneat as a digital tool for Validation activities within the project, we would like to organize
So…you have your Kneat Instance validated and you are eager to roll it out to all areas of your organization. Hold your horses and allow
Further to my earlier post on “No deviation and Paperless Validation: how it all began”, I wrote that No deviation has Kneat Academy certified Master
Since its incorporation in 2007, No deviation has supported clients in their CQV journey either in greenfield or improvement projects. No deviation constantly adapts and
Before diving into the topic of paperless validation in the pharmaceutical industry, the fundamentals of Good Documentation Practice (GDP) shall be reiterated. Data integrity, arguably
No deviation, a patient-centric solution provider for the pharmaceutical industry is pleased to announce its partnership with Kneat Solutions, the leading validation software solution for
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