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 ...

Developing a cleaning validation for a reusable medical device presents several challenges. How are you addressing them? "There have been many issues over the last 7 years, so there's increased ...

In pharmaceutical manufacturing, cleaning validation is an essential stage of verifying that the manufacturing process is suitable. As an integral stage of the cleaning validation program, analytical ...

An ISPE guidance document, four years in the making, brings risk-based thinking, statistics, and Lean Six Sigma to cleaning validation. leaning is such a basic concept that it may be difficult to view ...

The pharmaceutical industry is undergoing a transformative era driven by increasingly stringent global regulatory requirements, significantly impacting operational processes, particularly those ...

In this free webinar, learn how cleaning validation inefficiencies silently undermine overall equipment effectiveness (OEE), and how to fix them. Attendees will learn how capabilities like part-level ...

The pharmaceutical industry is undergoing a transformative era driven by increasingly stringent global regulatory requirements, significantly impacting operational processes, particularly those ...

This training is designed for those with responsibility for the design, execution, or validation of cleaning processes which may include operations managers and personnel, validation specialists, ...

The majority of food manufacturers would accept that cleaning is a vital function within food processing, especially with respect to issues of hygiene. However, cleaning is also a defining process in ...

This training is designed for those with responsibility for the design, execution, or validation of cleaning processes which may include operations managers and personnel, validation specialists, ...