Key features include stable software versions, controllable and planned updates, and an independent alarm system that continues to function even when the internet connection is interrupted.
The testo Saveris 1 Cloud centralizes measurement data from sensors, data loggers, and various locations onto a single platform. Through web-based dashboards, users can view current values, historical data, trends, and audit trails. The solution is based on existing hardware from the testo Saveris 1 range and can be scaled as needed, from individual measurement points to applications spanning multiple locations.
The system is designed for environments subject to stringent regulatory requirements and is compliant with GxP and FDA Title 21 CFR Part 11 requirements. This includes electronic signatures, access controls, and an audit trail, among other features. For validation, Testo provides documentation packages for Installation Qualification (IQ), Operational Qualification (OQ), and Functional Qualification (PQ).
Version Freeze and Alarms Even in Case of Connection Loss:
One of its key features is its unique Version Freeze architecture. Instead of continuous software updates, testo Saveris 1 Cloud operates with approved, long-term stable versions. A validated system configuration can be maintained for at least three years; customers decide when to upgrade. This reduces revalidation efforts and simplifies change planning in GxP-regulated environments.
For critical applications, the platform combines redundant data storage with an independent alarm system. This allows alarms to continue being sent via SMS, for example, even if the cloud connection is interrupted. This enables users to detect critical deviations even in the event of network or internet outages.
The centrally managed cloud-based approach reduces the tasks associated with on-premises servers, maintenance, backups, and updates. Furthermore, testo Saveris 1 can now also connect to external solutions, such as building management systems or laboratory information management systems.
In the pharmaceutical sector, the system is specifically designed for GMP environments, cleanrooms, laboratories, and other quality-critical processes. For production and storage areas, technical systems, and sensitive industrial processes, the platform offers the same compliance logic. Testo developed it to meet the stringent requirements of regulated pharmaceutical applications and has adapted it for other application areas.
