In this six-part blog series, we examine common issues with data transfer, integrity, analysis, reporting and storage that we encounter as cleanroom owners and users every day. We’ll explore how automation and electronic solutions, within the parameters of Regulatory Authorities and cGMP, can help improve efficiency and product quality.
In this six-part blog series, we examine common issues with data transfer, integrity, analysis, reporting and storage that we encounter as cleanroom owners and users every day. We’ll explore how automation and electronic solutions, within the parameters of Regulatory Authorities and cGMP, can help improve efficiency and product quality.
Upgrading is a streamlined process made easy by the FacilityPro® system’s user requirement specifications (URSs) of data integrity, automation, simplicity, integration, service and support.
Following the webinar, “Developing an Isolator Filling Line Using a Quality Risk Management Approach” the expert presenters answered questions around monitoring critical points in a cleanroom. Learn more…