SenseAnywhere is specialized in fully automated temperature monitoring for the Pharmaceutical Industry for years already. Soon our AiroSensors, in combination with our Pt100 smart probes, will be used to ensure safe distribution and storage of the long-awaited COVID-19 vaccines across Europe.
Seamless roaming with SenseAnywhere’s (mobile) AccessPoints installed at factory warehouses, distribution centers and inside transportation vehicles, allows 24/7 real-time monitoring of temperatures of the containers which contain the doses. The AiroSensor automatically transmits its data to the Cloud whenever it is in range of the network, without any human intervention.
Highly Accurate Cold Chain monitoring
The temperature data loggers meet the most stringent class of the EU regulation for data loggers EN12830:2018 accuracy class 0.2. The measuring equipment also has been calibrated to assure very secure and reliable monitoring of the temperature sensitive vaccines. A combination of the AiroSensor with Pt100 probe means you will have records of both the ambient temperatures as well as the (ultralow) temperatures at the vaccines themselves, enabling you to calculate how long the container will stay inside the required limits in its current state.
SenseAnywhere makes recalibration easy
Our smart Pt100 probes have intelligent connectors attached to them, meaning you can send in the Pt100 probes just by itself for (re)calibration. Periodical recalibration without monitoring gaps can easily be achieved by just swapping out the Pt100 probes that need to be calibrated with newly calibrated ones to keep a continuous monitoring chain. AssetTags on the outside of the transport cases will allow you to instantly get actual logger data and status on your smart device by just scanning the QR code on the tag.
SenseAnywhere offers a single source of temperature records from production until consumption. The user friendly and sustainable AiroSensors have a battery lifespan of 10 years, allowing uninterrupted usage for many years to come. We follow the rules of GAMP 5 and our software is validated and meets the regulatory requirements of FDA 21 CFR part 11.
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