Schneider Electric Software, a global leader in industrial software and part of Schneider Electric, the global specialist in energy management and automation, announces that customer Fujirebio Diagnostics, Inc. was placed in the Top 10 of the 2015 Workflow Management Coalition (WfMC) Global Awards for Excellence in Business Process Management (BPM).
The 2015 WfMC are Global Awards for Excellence in BPM and Workflow. The Workflow Management Coalition and BPM.com jointly sponsor the annual Global Awards for Excellence in BPM and Workflow. They recognize user organizations that have demonstrably excelled in implementing innovative business process solutions to meet strategic business objectives.
The 2015 WfMC Global Award for Excellence was given to Wonderware customer Fujirebio Diagnostics for implementing an equipment monitoring system based on Skelta BPM software to ensure compliance, and to meet extensive reporting and documentation requirements from regulatory authorities. The Wonderware Skelta BPM solution enabled Fujirebio to use Process Modeling for electronic equipment monitoring, underscoring their automated production management system.
“Our Electronic Initiative, based on Wonderware Skelta BPM, has helped us improve compliance with 21 CFR Part 11 and has increased overall productivity, saving about 1,100 man hours per year,” said Ken Kovacs, Quality Business Systems Manager, Fujirebio Diagnostics. He adds, “The BPM solution provides us with a collaborative infrastructure for other electronic data capture projects going forward.”
Wonderware Skelta BPM is an advanced business process management and workflow software that manages all activity flows that include people and/or systems inside or outside an organization. The sophisticated Business Process Management (BPM) application enables companies to model, execute, analyze and improve operational processes to drive higher levels of productivity, collaboration and innovation. Ideal as a cross-industry platform, Wonderware Skelta BPM solves the challenges within the Life Sciences industry for collaboration, visibility, compliance, and standardization of processes—all necessary to meet and exceed the requirements of 21 CFR Part 11 good manufacturing practice regulations.