Cleanroom Monitoring Systems

TSI Facility Monitoring Software (FMS) offers robust, reliable environmental monitoring specifically tailored for pharmaceutical and life sciences applications. With its distributed and flexible architecture, FMS ensures there's no single point of failure, safeguarding critical data access at all times. The software is designed for scalability, allowing users to expand monitoring as needs grow without extensive reconfiguration. FMS is also fully Pharma 4.0 ready, supporting OPC UA communication for seamless integration with other systems, ensuring compatibility with modern industrial standards. This approach means users have immediate access to essential data wherever and whenever they need it, supporting compliance, efficiency, and peace of mind in demanding environments.

Products

Facility Monitoring System with FMS Web Client

Access FMS Anywhere! OPC UA Client/Server functionality to monitor particle counts and other...

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A robust monitoring system is essential for life sciences environmental control. TSI cleanroom monitoring systems bring together remote particle counters and active air samplers to support continuous oversight, timely alarms, and comprehensive reporting in GMP-regulated spaces.

Configure sensors for Grade A/B zones and supporting areas to capture nonviable and viable data where it matters most. Define alarm thresholds based on risk assessments and procedures, then route notifications to operators and quality representatives. Dashboards present current status by room or line, while trend views assist with investigating excursions and correlating events with operational changes.

Key capabilities include:

  • Continuous nonviable particle monitoring with contextual trend analysis.
  • Integration of viable sampling devices for aligned reporting.
  • Role-based access and electronic records to support data integrity practices.
  • Standardized, audit-ready reports for batch documentation and quality reviews.

The system is designed to support life sciences workflows. Quality teams can review historical conditions, compare shifts and campaigns, and align findings with deviation management. Engineering and facilities can use trends to plan maintenance and optimize airflow strategies. Operations can access at-a-glance views to support area readiness decisions.

TSI systems are configurable to different manufacturing scales — from single suites to multi-building campuses. Start with critical points of control and expand coverage as requirements evolve. By unifying data from particle counters and viable sampling, life sciences manufacturers can strengthen contamination control strategies and help reduce the risk of unrecognized environmental events that impact production.


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