Paperless Validation

ISPE Good Pratice Guide: Digital Validation

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:

Upgrade of Kneat SAAS Platform – Why It Matters and How to Succeed

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

Kneat in Action: Beyond Traditional CQV Boundaries

Validation in the pharmaceutical industry is evolving fast — and Kneat is right at the heart of this transformation. Far beyond traditional Commissioning, Qualification, and

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

Digitisation in pharma CQV: How does it help?

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

Why pharma companies need paperless validation

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

Using Kneat in process validation for the pharma industry

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

Importance of governance in the implementation of Kneat’s paperless validation solution for the pharma industry

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