Insight and opinion

VALIDATE 2023: 9 Key Takeaways in an Era of Digitization & Change

By Art Gehring, VP Marketing, Kneat   As a new member of the Kneat team, I had the opportunity to…

Validation Workload Pressures Rise in 2023

Validation Workload Pressures On The Rise in 2023 Section One of the State of Validation 2023 report, People and Organizations,…

Validation Trends to Watch in 2024: Navigating the Evolving Landscape

In the dynamic world of pharmaceuticals, biotechnology, and medical devices, validation remains a cornerstone of ensuring product quality, safety, and…

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…

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 avoid the associated consequences.

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 the best way to digitize validation.

5 Key Takeaways From VALIDATE EU 2023

Building off the success of the inaugural VALIDATE conference in Boston last November, Kneat held its first annual European conference…

2023 State of Validation Survey: Share Your Voice

Navigating the evolving regulatory landscape requires an informed, efficient, and effective validation program. To help companies achieve this, we sponsor…

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 start your digital validation journey today.

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)

The Computer Software Assurance for Production and Quality System Software draft guidance stems from a multi-year collaboration between the FDA…

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