
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.
Resources

Learn how life sciences leaders are using validation to launch CAPEX projects faster and underbudget.

FDA's March 2026 draft guidance formalizes what a compliant Form 483 response requires.

Best practices for collaboration including lessons, challenges, and a readiness checklist.
Hilary Mills-Baker

Get Kneat's step-by-step framework for planning and executing a compliant validation platform migration.

State-of-the-art digital validation, built from the ground up.

Stay current with DVT upgrades to maximize performance, compliance, and value.
60 minutes
Sarah Grogan, Jon Thompson

See how MMR Consulting eliminates CQV rework using API-enabled TOP transfer with Kneat Gx.
60 minutes
Aaron Roth, Denis Bartley

See a live demo of Kneat Gx with the latest features and functions.
Emma Carey, Mark Foley

Enhanced Kneat Academy courses are here. Find the right training path for your role.