Support medicine integrity
Review temperature histories against product-specific storage requirements and give qualified teams evidence for assessment.
FOR PHARMACY, HEALTHCARE & DISTRIBUTION TEAMS
Give the people responsible for medicines a clearer view of the temperatures around them.
A medicine refrigerator can look normal while conditions inside it change. NanoTag and ThermoCloud help teams review recorded temperatures, recognise excursions and act through their quality procedures. Start with the requirements of the product, the storage location and the person responsible for responding.
Plan your pharmaceutical monitoring ↗
Responsible pharmacists · quality managers · hospital operations · pharmaceutical distributors
VALUE FOR YOUR ORGANISATION
Review temperature histories against product-specific storage requirements and give qualified teams evidence for assessment.
Configure limits and notifications, then agree who receives them and how the team escalates an issue.
Use downloadable reports alongside calibration evidence, operating procedures and documented decisions.
WHERE IT CAN FIT
Illustrative industry sceneMonitor selected medicine-storage points and give branch teams visibility beyond occasional manual observations.
Illustrative industry sceneSupport teams responsible for temperature-sensitive medicine storage across defined locations.
Illustrative industry scenePlace monitoring devices at locations selected through the site’s qualification or mapping process.
Illustrative industry sceneEvaluate suitable transport applications after checking packaging, sampling needs and LoRaWAN coverage.
THE RISK OFFICER’S VIEW
Monitoring works best when it is part of a clear operational process.
| Risk to consider | What the data can tell you | What your team owns |
|---|---|---|
| Power disruption or cooling failure | A rise or fall in recorded temperature may indicate an issue. | Investigate the equipment and follow the site’s stock-protection procedure. |
| Local hot or cold spots | Readings represent the sensor location, not every shelf. | Use qualified placement informed by the storage-area assessment. |
| An alert without an owner | Notifications alone do not establish that someone has acted. | Assign a primary responder, backup and out-of-hours escalation route. |
| Incomplete quality evidence | Graphs provide temperature information but do not establish product suitability. | Retain relevant records and obtain authorised assessment before disposition. |
HOW IT WORKS IN YOUR OPERATION
Place NanoTag near the qualified monitoring point. Activate it, confirm LoRaWAN communication and add the device to ThermoCloud. Configure product-appropriate limits, verify that intended recipients can receive notifications and establish a routine for reviewing reports. The standard published sampling interval is ten minutes; assess whether this meets the application’s requirements.
Explore NanoTag & the architecture ↗Illustrative scenario: a pharmacy team receives a notification that a monitored refrigerator location has exceeded its configured limit. The responsible person checks conditions, protects affected stock under the local procedure and provides the recorded history for qualified review. A return to normal temperature does not by itself confirm that the stock is suitable for use.
Process example, not a reported client case study.
PLAN THE RIGHT DEPLOYMENT
Discuss the current device revision, accuracy across the required range, calibration traceability, validation needs and record-retention requirements. NanoTag’s published range is −30°C to +60°C; ultra-low-temperature storage needs a different suitability assessment. Confirm any vaccine-programme device requirements before selection.
Independent guidance for planning. No endorsement of Thermologix or NanoTag is implied.
YOUR NEXT STEP
Tell us what you monitor. We’ll help you plan the right deployment.