The system that never sleeps
Seamless end-to-end monitoring for every environment – with testo Saveris 1
GxP-dokumentation og regulatorisk tryghed
I regulerede miljøer er dokumenteret kontrol ikke et valg – det er et krav. Vores løsninger understøtter efterlevelse af gældende GxP-retningslinjer og sikrer, at dine kritiske måledata håndteres i overensstemmelse med internationale standarder.
Med Testo Saveris får du et validerbart overvågningssystem, der er udviklet til brug i GMP-, GDP- og GLP-regulerede miljøer. Systemet understøtter:
- Overholdelse af EU GMP Annex 11
- FDA 21 CFR Part 11
- Sporbarhed & audit trail
- Dokumenteret kalibrering og valideringsunderstøttelse (IQ/OQ)
Automatiseret overvågning, alarmering og dokumentation reducerer risikoen for menneskelige fejl og sikrer, at temperatur-, fugt- og andre kritiske parametre overvåges kontinuerligt.
Confidence through control
Testo Saveris 1 stands guard over your critical environments, day and night. Temperature, humidity or pressure – every parameter is monitored and recorded with absolute precision. The system stays alert, detects even the smallest deviation, and raises an alarm before thresholds are exceeded.
All data is captured automatically and available in real time, ensuring full compliance and complete peace of mind 24/7. The latest software update brings smarter automation, reinforced security, and greater flexibility to keep your monitoring sharp, reliable and ready for the future.
Key Features
testo Saveris 1 never stops monitoring. And at Testo, we never stop improving our solution. With the latest software release, your system is now even smarter, more secure, and easier to use. Discover the new features below and learn how to take your monitoring to the next level.
Automated workflows for efficient monitoring
Create workflows with actions in sequence such as activation and deactivation of alarms and webhooks
Save time with scheduled routines that match operating hours and support SOPs
Gain transparency and security through central configuration and alerts on failed workflows
Approvals for secure and compliant changes
Set up multi-level approvals for actions such as alarm acknowledgement or configuration changes
Strengthen compliance with clear approval chains, accountability, timestamps, and transparent audit trails
Reduce risks and stabilise operations through controlled and transparent change management
Flexible control of webhooks
Activate or deactivate webhooks without deleting configurations
Use webhooks manually or as part of automated workflows
Save time by reactivating existing setups whenever needed
Single sign on for seamless and secure access
Use corporate login for fast access and fewer passwords
Increase security with central policies and conditional access
Simplify administration through automatic role mapping and audit ready identity management
Sensor. Software. Services.
testo Saveris 1 combines measurement excellence in an end-to-end solution.
testo Saveris 1 combines sensor, software and service in a complete, validatable monitoring solution. High-precision sensors continuously record critical environmental data and ensure long-term stability through robust design and rigorous quality testing. The software automates workflows and alarms, reduces manual work and provides clear dashboards and reports so that patterns and deviations are quickly identified. All measurement data is analyzed securely and in accordance with FDA 21 CFR Part 11 and EU GMP Annex 11.
The solution is supported by targeted service concepts, including validation, training, calibration, maintenance and ongoing system checks – as well as a flexible helpdesk and expert advice that ensure stable and compliant operation in everyday life.
New whitepaper
How to master biotech monitoring
Biotech processes require absolute precision to keep products stable. Meticulous monitoring is therefore key to quality and regulatory confidence. Our latest whitep aper shows common challenges faced by our Biotech clients when monit oring their assets and showcases two r eal use cases that have addressed those challenges.
More measurement knowledge
A compact reference with key terms and definitions for GxPcompliant transport processes.
Biotechnological processes require absolute precision. This whitepaper shows how documentable monitoring ensures product stability and regulatory compliance in practice
This whitepaper provides a comprehensive overview of Application Programming Interfaces (APIs) and webhooks and analyzes their use for efficient, real-time data integration and interoperability in modern systems.
testo Saveris 1
Discover our services
Our specially GxP-trained service team provides comprehensive support throughout every process step – from planning and documentation to qualification, validation, and ongoing operation. We develop tailored service concepts to meet your specific requirements and ensure continuous GxP compliance. With our expertise, you can rely on efficient system maintenance, r eliable monitoring, and consistently high quality standards.
