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Select between storage monitoring and transport monitoring.
Legal requirements and the safety of patients and consumers require the proper transport and correct storage of temperature-sensitive products. Our devices guarantee reliable storage and temperature monitoring and therefore the continuous monitoring of the entire supply chain. Depending on the intended use and legal (cantonal) requirements, devices are required to have either validation or calibration certificates.
Since January 2016 the international rules of Good Distribution Practice (GDP) apply in Switzerland. As part of the quality assurance process, GDP ensures that drug quality is preserved throughout the entire supply chain, including via the monitoring of the legally-required temperatures.
Validation offers the certainty that processes, methods or systems provide constant results according to established criteria. Calibration proves that instruments or devices provide results within defined limits. The decisive values are those obtained using a reference standard or reproducible standard via an appropriate sequence of measurements.