A facility monitoring system that can be set in a wide range of settings so that it can meet the management needs of various industries such as pharmaceutical manufacturing
Beckman Coulter Life Sciences
About This Product
The facility monitoring system (FMS), which remotely perform facilities monitoring, is able to make a wide range of settings so that it can meet the needs of clean rooms in various industries, such as pharmaceutical manufacturing. FMS can monitor the number of floating fine particles, air temperature, and relative humidity in non -biological air.
Our FMS solution is based on an open architecture platform designed to make it easy and efficient to integrate with the SCADA system that you already have.
Routine monitoring and clean room classification portable party counter "MET ONE 3400 Series" and remote -type intermediate counter "MET ONE 6000 Series" are all designed based on the established technologies of MET ONE Technology. I am. MET ONE Software Aplatform has intuition and easy -to -use interfaces, reducing human errors that can be caused by manual SOP monitoring.
In addition, it is possible to integrate monitoring reports and to adapt to the eugmp/FDA various guidelines (for example, ISO 14644 and 21 CFR Part 11), and integrate FMS data to an electronic signature report.
■ Data management
・ Integrate multiple monitoring systems to prepare verification, maintenance and data management
・ Eliminates a single obstacle by redundant data management
■ Software
・ Simple interface for monitoring neutral particle count monitoring and reporting
・ Installing and setting of a wizard base of the count
・ One -touch report creation
・ IQ / OQ document template
■ Service options
・ Local service staff provides on-site ISO 21501-4 to school positives and services
・ Service contract option for calibration and maintenance on on -site on -site by advance reservation (including repair discounts)
■ Compliance
・ ISO 14644 Clean Room Management
・ ISO 21501-4 Correction for accuracy and reproducibility between sensors
・ 21 CFR Part 11 regarding the management of electronic data records
・ EU GMP Annex 1 for sterile drug production
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Product
A facility monitoring system that can be set in a wide range of settings so that it can meet the management needs of various industries such as pharmaceutical manufacturing