Insight and opinion

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

ISPE Singapore – Aug 23–25, 2023  The ISPE Singapore Affiliate Conference & Exhibition highlights the best practices and services—from manufacturing facility…

Validation software is an essential tool for companies that need to validate their processes and equipment quickly and efficiently while…

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.

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.

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

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

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.

Digital maturity in manufacturing is an increasingly important aspect of commercial performance in the life sciences industry today. In this…

As life sciences manufacturers continue to seek efficiencies in processes through computer systems, demand to install and maintain an array…

The Computer Software Assurance for Production and Quality System Software draft guidance stems from a multi-year collaboration between the FDA…

Critical to the success of implementing a digital validation solution, is the ability to communicate its business and financial benefits,…