One Excursion Can Cost Millions. Omnia Makes Sure It Never Happens. In pharmaceutical logistics, a single temperature excursion can trigger recalls, regulatory investigations, and losses running into millions. Omnia is a GDP and CFR 21 Part 11 compliant platform built for pharmaceutical manufacturers, clinical trial logistics, and life sciences supply chains. From passive dataloggers to real-time satellite trackers, every device, every partner, every shipment mode are unified in one audit-ready platform.
Omnia connects passive dataloggers and real-time trackers from any hardware manufacturer — no vendor lock-in, no replacing existing equipment. If it tracks, Omnia reads it.
Elevated CO2 levels inside a shipment can compromise pharmaceutical products before a temperature excursion ever occurs. Omnia monitors CO2 continuously alongside temperature and humidity and gives a complete picture of the environment your product is travelling in.
Whether your tracker communicates via satellite, 5G, 4G, NFC, Bluetooth, or RFID.Omnia receives the data. No connectivity gap, no matter where your shipment travels.
Pharmaceutical shipments rarely move on a single mode. Omnia tracks across all three air, road, and ocean with no visibility gap between handoffs.
Every shipment is monitored in real time for temperature, humidity, light exposure, and shock the parameters that determine whether your product arrives intact.
Every temperature spike, humidity breach, and handling event is timestamped and location-tagged throughout the journey. When a deviation occurs, Omnia tells you exactly where it happened, at what point in transit, and which actor was responsible.
Mix real-time trackers and passive dataloggers on the same shipment. Omnia handles both simultaneously, independent of transport mode.
Set clear user profiles aligned with your organizational structure and logistics workflows.
Whether it's a primary manufacturer, a clinical trial site, or a last-mile courier — every handoff is tracked, every milestone is recorded, and nothing falls through the cracks.
The moment a threshold is breached, your entire team is notified simultaneously — no manual checking, no delay. Act while the shipment is still in transit, before a deviation becomes a loss.
If a shipment leaves its approved route or crosses an unauthorized boundary, Omnia flags it immediately. Know where your product is — and where it shouldn't be.
Traditional systems tell you what went wrong after delivery. Omnia tells you while the shipment is still in transit — giving you the window to act before product integrity is compromised.
Omnia generates a single, unified shipment report — covering every device reading, every milestone, every partner action, and every excursion event. No consolidating data from multiple systems.
Every report includes calibration certificates for all devices used and CAPA documentation where required. Everything your QA team needs, in one place.
Every action taken within Omnia is logged who accessed the shipment, what was changed, when it happened. Full transparency from start to finish.
For pharmaceutical companies operating under FDA and international data integrity regulations, Omnia's electronic records and audit trail meet CFR 21 Part 11 requirements in full.
Omnia is fully validated to meet Good Distribution Practice standards. Every shipment report is GDP-ready no additional preparation required before an audit.
Because every shipment matters.
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