Resource center

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....

How Dechra streamlined C&Q and CSV

Understand how Kneat’s partnership with global validation services provider VEQTOR enabled leading animal health company Dechra Pharmaceuticals PLC to eliminate....

Integrating digital validation

See how to integrate data with Kneat Gx to deliver more value in this webinar.  

Accelerating CQV: streamlining processes for a paperless future

As part of its top-down digital strategy, a Top 10 global pharmaceutical and healthcare company implemented Kneat to digitize CQV....

Managing equipment lifecycles

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....

Overcome validation challenges

Overcome compliance challenges through digital validation. Learn proven strategies, real-world insights, and tools to streamline processes in this webinar.

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....

The 3 stages of process validation

Process validation is the bedrock of good manufacturing practice, it’s also the first step to realizing significant time and cost....