
Case Study: How No deviation Helped Achieve a Smooth Kneat Upgrade (v8.8 to v9.3)
A leading pharmaceutical client, using Kneat since 2019, partnered with No deviation for a critical upgrade from version 8.8 to 9.3. Their goal: improve system

A leading pharmaceutical client, using Kneat since 2019, partnered with No deviation for a critical upgrade from version 8.8 to 9.3. Their goal: improve system

Digital Validation Takes Center Stage April 2025 marks a major milestone in the pharmaceutical and life sciences industries: the publication of ISPE’s Good Practice Guide:

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
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