MET ONE Facility Monitoring Systems
Scalable on-line particle monitoring solutions based on open architecture communications that integrate easily with your preferred systems.
- Suite of air particle counters
- Integration software
- Full ISO 21501 compliance
- 21 CFR Part 11 compliance
- On-site service option
MET ONE Facility Monitoring System Overview
We provide scalable Facility Monitoring Systems (FMS) that can be configured to meet a wide spectrum of cleanroom management needs for various industries—including pharmaceutical production. Among parameters that can be efficiently and reliably monitored using a Beckman Coulter FMS are non-viable/viable air sampling, differential pressure, air temperature and relative humidity. All of the company’s FMS solutions are based on an open-architecture platform designed to enable easy, streamlined integration with existing customer systems (SCADA). Each instrument is built around proven MET ONE technology, including the portable MET ONE 3400 series for routine monitoring and cleanroom classification, as well as the 6000 and 7000 series of fixed, non-viable air particle counters. MET ONE software platforms feature intuitive interfaces to help make them easy to use, thereby reducing the potential for human error that can occur with manual SOP monitoring. To avoid losses from product contamination, stack lights, audible alarms and process shutdown signals from a Beckman Coulter FMS can prompt an immediate production line response whenever an excursion happens. In addition, to help centralize reporting and simplify EUGMP/FDA compliance (e.g., for ISO 14644 and 21 CFR Part 11), Beckman FMS data can be integrated into a single-release, electronically signed paperless report.
- Workflow-optimized, integrated solutions to monitor your cleanroom
- 21 CFR Part 11 enabling software workflow to ensure secure data management
- Integrate portables and remote air particle counters
- Industry standard interfaces (OPC, ODBC) for integration with other systems
- Support for 32 location manifold integration for automated routine environmental monitoring
Features
Particle Monitoring Compliance
- Nonviable and viable particle monitoring compliant with EU GMP
- Annex 1 and FDA 21 CFR Part 11
- Built in Audit Logging
- Custom reports to record results
- IQ/OQ documentation for simple validation
Scalable Solutions
- Small scale, rapidly deployed pre-packaged software and hardware for isolators and small production line
- Batch workflow system for one or more production lines with several monitoring points
- Custom workflow optimized solutions for monitoring complex production methods across several production lines
Service Options
- Regional Service Professionals provide onsite ISO 21501-4 calibration and service
- Service agreement options for pre-scheduled onsite calibration and maintenance (including discounts for repairs)
Ease of Use
- Graphical user interfaces available on the system or via remote access terminals
- Color coded indication of system status
- Alarms clearly identified for acknowledgement
- Single click reports to generate auditable records for compliance