Discover how automation is revolutionizing laboratory processes, changes in the regulatory landscape, and how labs can stay ...

Regulatory agencies expect companies to establish and monitor clean equipment- and dirty equipment-hold times for manufacturing equipment as part of their cleaning validation program. The concepts of ...

The author explains the idea of equivalence and describes how it can facilitate equipment validation. It is common in the global healthcare industry to have multiple pieces of identical equipment ...

Qualification/validation can be defined as “establishing documented evidence which provides a high degree of assurance that specific equipment procured will ...

“We continue to build strong momentum in new customer acquisitions, further cementing our leadership as the global standard for validation lifecycle management. This strategic win reinforces Kneat’s ...