The new Kneat Gx: more than validation
Validation software is an essential tool for companies that need to validate their processes and equipment quickly and efficiently while....
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Top reasons for form 483s and warnings
See the top reasons for receiving FDA 483s and warnings. Learn how to take necessary steps to prevent non-compliance and....
Optimizing validation processes for digitization: why paper to glass isn’t enough
When optimizing validation processes, it’s not enough to just go from paper to glass. Learn why paper to digital is....
5 key takeaways from VALIDATE EU 2023
Explore the top 5 takeaways from Validate EU 2023 in our detailed article. Delve into the latest insights and trends....
2023 state of validation survey: share your voice
Join our annual industry survey to benchmark and enhance your validation programs. Gain insights from global validation data across industries,....
The true cost of delaying digital transformation in validation
Starting a digital transformation can seem daunting, but the cost of delaying it is far worse. Learn why you should....
Why digital maturity in manufacturing underpins commercial performance
Digital maturity in manufacturing is an increasingly important aspect of commercial performance in the life sciences industry today. In this....
How Kneat meets 21 CFR Part 11 and unlocks additional benefits
As life sciences manufacturers continue to seek efficiencies in processes through computer systems, demand to install and maintain an array....
5 things you need to know about computer software assurance (CSA)
Read this article to discover five things that you need to know about Computer Software Assurance (CSA) and how to....