LIMERICK, Ireland, Jan. 06, 2026 (GLOBE NEWSWIRE) -- kneat.com, inc. (TSX: KSI) (OTCQX: KSIOF) , the global leader in digital validation and ...

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

Cleaning of pharmaceutical equipment is essential to reduce the risk of product contamination and, as stated in relevant guidelines and as recognized by the pharmaceutical sector, this can be achieved ...

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 ...

Validation engineers design or plan protocols for equipment or processes to produce products meeting internal and external purity, safety, and quality requirements. Natural problem-solvers, ...

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