By Debbie Francis, Principal Consulting Product Marketing Manager, Waters Corporation
Quality Control (QC) labs face stringent and continuously evolving compliance and data quality requirements to release products within tighter budgets and timelines. In the increasingly fast-paced race of new therapeutic development, remaining competitive is constantly at the forefront of pharmaceutical company leaders’ minds. To accomplish this goal, they prioritize increasing productivity and searching for new strategies to implement in their lab environments. Here, we examine the cause and impact of common lab errors, the strategy for reducing those errors with an intuitive chromatography system, user-driven insights that shaped the development of the Alliance™ iS HPLC System, and the financial and operational benefits of investing in the system.