
ISPE’s Good Practice Guide is out — and No deviation Is Proudly Involved
Digital Validation Takes Center Stage — And No deviation Is Proudly Involved April 2025 marks a major milestone in the pharmaceutical and life sciences industries:
Digital Validation Takes Center Stage — And No deviation Is Proudly Involved April 2025 marks a major milestone in the pharmaceutical and life sciences industries:
The pharmaceutical industry is under constant pressure to deliver safe, compliant products while accelerating time-to-market. Traditional paper-based validation processes are time-consuming, error-prone, and difficult to
Validation in the pharmaceutical industry is evolving fast — and Kneat is right at the heart of this transformation. Far beyond traditional Commissioning, Qualification, and
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
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