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.
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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.
16:00 (60 minutes)
Emma Carey
Resources
Med Device Solutions for 2026
Explore CSV approaches for med device companies & how to build processes
60 minutes
Kathianne Ross, Tim Akin
CSA Final Guidance Decoded
Final CSA guidance is here with significant changes to Computer System Validation.
16:00 (1 Hour)
Lorna Whelan
Speed Up Your CQV Process
Koerber Pharma and Kneat discover how validation expertise can jumpstart CQV
60 minutes
Preparing for GMP Updates
Kneat experts talk about the most significant updates to GMP guidelines in years
60 minutes
Stefan Münch
Standardize Globally, Adapt Locally
See how to balance harmonization and flexibility in this ISPE best practices webinar.
1 hour
Amy Wilhite, Art Gehring
Supercharge your C&Q
MMR shows the benefits of adding Integrations to your digital C&Q validation.
60 minutes
Aaron Roth, Denis Bartley
Operational Readiness in Pharma
Kneat and PM Group share how digital validation reinforces operational readiness to build concrete GMP compliance and accelerated tech transfer....
60 minutes
Michael Sweeney, Fintan Coady
USP <665> Unlocked: Your 2026 Compliance Playbook
See how to meet USP compliance by 2026 with expert guidance from ALTEN & Kneat.
60 minutes
Olivia Calder, Stan Van Kerkhoven
Validation in Transition: 2025’s Top Trends, Tools, and Takeaways
Join experts to unpack 2025 validation trends, challenges, and digital adoption.
60 minutes
Joe Azzarella, Darragh Boyle, Jamie O’Donnell, Tim Akin