Automated management from visualization to alerts and recording! Environmental monitoring system.

GxP compliance! An environmental monitoring system that centrally manages inspection-related environmental parameters.

The testo Saveris 1 centrally manages all environmental parameters related to inspections of life science applications quickly, efficiently, and easily. It is an environmental monitoring system that allows for the construction of a flexible system combining wireless and wired networks. It adopts a wireless frequency that reaches a wider range and can manage up to 1,000 loggers. In addition to Testo loggers, it can also incorporate electrical signals from incubators and other devices from different manufacturers into the Saveris system, enabling centralized management of various types of data. It can operate in low-temperature ranges, supporting temperatures down to -200°C, making it suitable for ultra-low temperature freezers. The CFR software complies with FDA requirements for 21 CFR Part 11 and EU GMP Annex 11. The data management platform can accommodate any type of inspection and is accessible from around the world, utilizing flexible alarm settings, reporting features, and database hosting options to enable comprehensive analysis and management of all recorded measurement parameters. *For more details, please download the PDF or feel free to contact us.*

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basic information

The dedicated database system efficiently manages measurement data such as temperature and humidity. The data can be grouped arbitrarily, such as by the installation location of the loggers, making it easy to retrieve the necessary information. Additionally, management from multiple PCs over the network is possible. The alarm function can be set in two stages: pre-alarm and main alarm, and it also supports delay settings. Notifications can be sent via email, and it is possible to connect to warning lights using contact signal output. Furthermore, we offer dedicated software with enhanced data management features called "PRO Software," as well as "CFR Software," which complies with FDA 21 CFR Part 11. 【Common Software Features】 ■ Graph/List/Alarm Overview/PDF Report ■ Data management using calendar functionality ■ Setting and displaying probe groups ■ Alarm notifications (email, SMS, relay) ■ Alarm management in stationary mode ■ Display of layout diagrams for measurement locations 【Additional Features of CFR Software】 ■ New Cockpit ■ Electronic Signature ■ Issuance of three levels of access rights ■ Audit Trail *For more details, please feel free to contact us.