Skip to content
FOR PHARMA & COLD CHAIN

GxP-grade evidence for hazardous pharma logistics.

Class 6.2 infectious substances, Class 9 dry ice, lithium-powered IoT loggers — DGM One captures the chain of custody auditors expect, integrated with your QA and TMS systems.

PAIN POINTS WE SEE

What's slowing pharma down today.

  • Dry ice and infectious substances misfiled at handoffs
  • Lithium-powered IoT loggers double-classified or missed entirely
  • Audit trails fragmented between QA and logistics systems
WHAT CHANGES

From manual patchwork to evidence-by-default.

  • Class 6.2 / 9 templates with packaging defaults
  • IoT logger profiles + per-shipment battery accounting
  • QA-ready export packages signed and timestamped
MODULES MOST RELEVANT

The DGM One pieces that matter most here.

AI-Assisted Classification

Identify UN numbers, hazard classes, packing groups, and special provisions from product names, SDS, or photos. Variations are applied automatically per mode.

Multi-Modal Declarations

Generate IATA, IMDG, ADR, and 49 CFR documents from a single shipment record. PDFs, labels, marks, placards — all version-controlled.

Lithium Battery Toolkit

30% SoC validation, UN 38.3 documentation, Section II rules, packaging look-ups, and incident response cards — the most common point of failure.

Audit-Ready Evidence

Tamper-evident event logs, signed PDFs, and complete chain of custody. Export an audit package for any shipment in one click.

See all modules
EXPLORE OTHER INDUSTRIES

DGM One is built to flex across the chain.

GET A WALKTHROUGH

See DGM One on your own shipments.

Bring a real shipper's declaration. We'll show you classification, document generation, and audit export live — in under 30 minutes.