RMS Applications

Cleanroom & Chamber Monitoring

Ensure cleanroom compliance with Rotronic Monitoring System (RMS)

The Rotronic Monitoring System (RMS) ensures cleanroom compliance with standards like ISO 14644, GMP Annex 1, and FDA regulations. It monitors critical parameters such as temperature, humidity, and differential pressure, vital for maintaining aseptic conditions and product quality. RMS offers a scalable solution that integrates sensors and particle counters, providing secure data handling, detailed analytics, and configurable alarms.

Contact Us
Cleanroom Requirements

Stringent control over environmental factors like air contamination and pressure is essential in cleanrooms. Regulatory frameworks, including ISO 14644 and GMP Annex 1, highlight the importance of precise monitoring to prevent contamination, especially from human operators—the primary source of microbial risks. Devices into cleanroom need also to be monitored, as incubators, climatic chambers, or glovebox on parameters as temperature, CO2, O2, humidity to ensure control of the production or tests. RMS can cover all in one system.

How RMS Supports Compliance

RMS is a powerful environmental monitoring system compliant with ISO 14644-2, EudraLex Annex 11, and FDA 21 CFR Part 11.

Key Features
  • Real-Time Monitoring: Tracks deviations in critical parameters.
  • Configurable Alarms: Set thresholds with delay and hysteresis options.
  • Data Analysis Tools: Identify trends and correlations to optimize performance.
  • Calibration Management: Ensures traceability and compliance, Calibration/adjustment function, calibration due date alerts
  • Flexible Integration: Supports third-party devices and a wide range of sensors.
Download free White Paper: “Data integrity, ALCOA+ and the power of digitization”
Why choose Rotronic RMS

RMS simplifies cleanroom management, enhances efficiency, and protects product integrity. Its robust, user-friendly design ensures organizations meet international compliance standards effortlessly.