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Merck Sharp & Dohme (MSD) reduced validation time by 50%
MSD digitized seven validation processes globally, reducing cycle times by 50%, process steps by 46%, and replacing three QMS systems.
The 2025 digital validation handbook
Find out everything you need to know about how to streamline validation, leave paper-based processes behind, mitigate noncompliance risks, and....
Kneat Gx: Software Demo
See a live demo of Kneat Gx with the latest features and functions.
15:00 (60 minutes)
Mark Foley
FDA’s final CSA guidance
Discover 9 key changes in FDA’s final CSA guidance — and how Kneat Gx supports them.
Kneat ranked best pharma and biotech software
G2 has ranked Kneat best pharma and biotech software in Grid report, rating Kneat as the top pick in satisfaction....
Medical device validation in 2025
Discover key MedDev insights and strategies from the 2025 State of Validation industry study.
How Kneat Gx enables data-centric validation
Learn how Kneat Gx enables data-centric validation.
Why digital validation is working — and where it still falls short
Why digital validation works — and what’s still holding teams back in 2025.
Breaking down the ISPE digital validation guide
Kneat brought together two of the co-authors to examine the new ISPE Digital Validation guide for DVTs and what it....
FDA Warning Letters – How to Avoid & What to do If Received
FDA Warning Letters - How to Avoid & What to do If Received
How to choose digital validation software
See how CAPEX budgets can be trimmed through digital validation.
Commissioning and Qualification in Pharmaceutical Facilities
How is C&Q different for pharma facilities? We explore in this blog.