The pillar document of C&Q in the pharma industry
Our previous blog posts talked about the skills needed to be a C&Q engineer and the 7 guides you should read. This blog talk about
Commissioning, Qualification and Validation
The 7 guides to unlock a successful risk-based CQV project
Our previous post talked about the skills a CQV engineer needs. In this article, we will give you the CQV starter kit with 7 documents
FAT Protocol Development:
Option 2 – Using Test Case Library
Hi there. This is Joon, your trusted Kneat partner. Thank you very much for clicking into another instalment of my vlog where I’m continuing to
FAT Protocol Development:
Option 1 – Client imports Word document provided by vendor
Hi there! This is Joon from No deviation, your trusted Kneat partner. I’d like to share with you today, one of the many different methods that can
A practical guide to lean CQV (Commissioning, Qualification, Validation)
Through the many different iterations of the CQV model, from the traditional V-model to the hybrid approach to the risk-based approach, a significant amount of time and effort has been spent demonstrating to regulatory inspectors…
What you need to become a CQV engineer in the pharma industry
In our previous posts, we explained why there is no better time than now to work in the pharmaceutical industry. It is especially true for
No deviation and Paperless Validation: how it all began
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
What is Design Qualification
How many of us have seen this circulating comic strip and smiled to ourselves, knowing that this is exactly the situation at work – whether
Commissioning and Qualification in the pharma industry: debunking the 5 myths
Over the years that I have been working, starting as a junior C&Q engineer, there has been an increasingly blurred line between Commissioning and Qualification
What is paperless validation in the pharmaceutical industry
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
