Technology & Monitoring

Cold chain integrity through real-time technology

From sensor to dashboard — our pharma technology captures every data point in your shipment's journey, analysed and documented. No gaps, no guesswork.

Temperature Management

Five temperature zones, one monitoring standard

Pharmaceutical products span a thermal spectrum from controlled room temperature to cryogenic storage below -150°C. Each zone demands specific packaging, monitoring equipment, and handling protocols.

Every zone is GDP-qualified. Packaging is validated against specific route profiles, accounting for seasonal variation and transit duration.

End-to-End Visibility

From collection to delivery — every step monitored

Temperature logging begins the moment we take custody of your product and continues uninterrupted until final handover.

1
Collection

Pickup from client facility; packaging checked and sealed

2
Logging Start

Data logger activated; temperature baseline recorded

3
In Transit

GPS tracking; continuous monitoring; alerts active

4
Delivery

Temperature verified at handover; digital signature captured

5
Documentation

Audit-ready packet compiled and delivered with shipment

Control Tower

Real-time shipment intelligence

Track every shipment across its full journey — temperature, route, and compliance events in one view, filterable by time range.

Live Monitoring
Connected --:--:--
Time Range
Temperature (°C)
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Capabilities

Real-time pharma technology monitoring features

GPS Tracking

Continuous location data with geofencing alerts for route deviation detection.

Temperature Alerts

Instant notifications when readings approach defined thresholds — before an excursion occurs.

Digital Documentation

Automated generation of transport records, temperature certificates, and compliance reports.

Chain of Custody

Timestamped handover records with digital signatures at every transfer point.

Excursion Management

MKT analysis, stability data cross-reference, and automated CAPA initiation.

Audit Trail

Complete, immutable record of every event — from sensor calibration to final delivery.

Validated Packaging

Packaging systems matched to your product

The right packaging is not about choosing the most expensive option — it is about matching thermal performance to your product's stability profile, transit duration, and route conditions.

Passive Systems (PCM)

Phase change materials maintain target temperature for 48–120 hours without external power.

Active Containers

Electrically powered units for extended transits requiring precise temperature control.

Vacuum Insulated Panels (VIP)

High-performance insulation reducing thermal conductivity by up to 10× versus standard foam.

Cryogenic Dewars

Liquid nitrogen vessels for cell and gene therapy shipments below -150°C.

Qualification Process

1
Product stability profile analysis
2
Route and season assessment
3
Packaging selection and thermal modelling
4
Performance Qualification (PQ) testing
5
Ongoing monitoring and revalidation

Revalidation cycles: Packaging qualification is reviewed quarterly and after any significant route or product change.

Innovation

Technology that anticipates problems

Reactive monitoring catches excursions after they happen. Our approach uses predictive analytics to prevent them.

Coming 2026

Predictive Analytics

Historical route data combined with weather forecasts and traffic patterns to identify risk windows before shipment dispatch.

IoT Sensor Network

Multi-parameter sensors capturing temperature, humidity, shock, light exposure, and tilt — transmitting at configurable intervals.

Automated Compliance

Digital documentation systems that generate audit-ready packets automatically, eliminating manual data entry errors.

See it in action

Experience our monitoring technology first-hand

Request a live demonstration of our shipment tracking and temperature monitoring capabilities.

Request a Demo