High quality standards in production and storage necessitate a comprehensive monitoring system that delivers measured data reliably. The adaptive RMS is the perfect solution for a wide range of applications.

The RMS is a modular system of hardware elements and web-based software. The data loggers record measurements from Rotronic and third-party sensors and transmit them via a LAN or wireless interface to the secure database. It stores information, system actions and makes it available to users, regardless of whether they access the database via a PC, Mac, tablet or smartphone. The data can be accessed from anywhere in the world as long as an internet connection is available. The RMS Server Software fulfills requirements for server-based monitoring.

The RMS is perfect for both large monitoring systems and for simple, small applications. It provides maximum flexibility in installation and ensures readily available data. Full range of individual components and software are available for the monitoring system. The database is available as a secure cloud account. We also offer professional advice, installation, commissioning and maintenance for the installed RMS.

FDA/GMP Requirements:
Regulators in the pharmaceutical and food industries demand that all relevant events are recorded so they are traceable. This is achieved through the electronic marking of all calibration measurements and verification processes. The so-called "electronic recording" requires unique identification of certificates. This means that every calibration certificate with a date and inspection stamp must be traceable such that the calibration chain can be verified.

Audit Trail:
When a monitoring system is commissioned, it is calibrated and validated. In this way the operator assures his Quality department that the system works correctly. During subsequent operation, all relevant changes must be recorded in full. The audit trail guarantees recording of all changes in the system such as, for example, change in measurement probes, user activities, battery change. This in turn ensures that all events can be tracked at a later date.

• GMP/GLP/GDP compatibility
• FDA 21 CFR Part 11 compatibility
• EN 12830 compatibility
• Data History Always Available
• Data Security, Data Integrity & Data Availability
• PDF report with chart and statistics
• Alarm notification by voice call, SMS or email
• Platform independent
• Validation At The Touch Of A Button
• Easy User Management
• Suitable for smart-phones and tablets
For comprehensive monitoring in production and storage facilities of pharmaceutical and food industries.
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