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 show you how can we prepare an FAT protocol. We have seen in the previous vlog that we can prepare the FAT protocol by importing a Word document into the…
FAT Protocol Development:
Option 2 – Using Test Case Library Read More »
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 be used to develop Factory Acceptance Test or FAT Protocol in Kneat, the world’s most advanced paperless validation solution. Given the scenario that you are the equipment manufacturer and the client, in this
FAT Protocol Development:
Option 1 – Client imports Word document provided by vendor Read More »
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…
A practical guide to lean CQV (Commissioning, Qualification, Validation) Read More »
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 validation solution within an organisation that brought attention to the struggles of a paper-based approach. In this post, let me share with you what I think are the top 7
Why pharma companies need paperless validation Read More »
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 a meeting with No Deviation who is already involved in the C&Q Initiative Kneat Deployment. The aims of this session are: To explore the benefits of using Kneat To discuss
Using Kneat in process validation for the pharma industry Read More »
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 me to share with you the key considerations before scaling up and out, on the use of the world’s most advanced validation technology, KneatGx. Why the need for Kneat Governance?
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 Trainers and can deliver training to the same high standards as Kneat Academy. Let us look more into why you should be considering No deviation as your partner towards discovering
Paperless Validation training for the pharmaceutical industry with No deviation Read More »
1. Tell us more about your role at No deviation. It would be a very long story if I had to detail all my activities at No deviation. I do a bit of everything, from optimising back office operations to business development, running a project and keeping the CEO in check. Jokes aside, my role
Talk to the expert: JoonLeong Ng, Director, No deviation Read More »
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 applies the latest industry knowledge and tools to accelerate the CQV effort and ultimately benefit patients. In the recent ISPE Global Regulatory Pharmaceutical Summit held on 28 April 2021, David
No deviation and Paperless Validation: how it all began Read More »
How many of us have seen this circulating comic strip and smiled to ourselves, knowing that this is exactly the situation at work – whether you are the engineer or the user? I am using this example as an opening to the topic as most of us can relate to it at the most basic
What is Design Qualification Read More »
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