Clinical Trial Courier

Precision logistics for clinical research

Time-critical, chain-of-custody controlled transport for investigational medicinal products, biological samples, and trial supplies.

Logistics Flow

End-to-end clinical trial logistics

Follow the journey from sponsor release to site delivery and sample return.

Trial Phases

Tailored to every study phase

I

Phase I

First-in-human studies at single centres. Small volumes, highest urgency, same-day courier capability.

  • Single-centre delivery
  • Small batch handling
  • Priority same-day service
II

Phase II

Efficacy studies across multiple sites. Growing complexity with multi-site coordination.

  • Multi-site distribution
  • Randomisation kit management
  • Temperature monitoring per site
III

Phase III

Pivotal trials at scale. High volumes, international sites, regulatory scrutiny.

  • Global distribution network
  • Regulatory documentation per country
  • Large-scale IMP logistics
IV

Phase IV

Post-marketing surveillance. Ongoing supply with established logistics pathways.

  • Routine supply chain
  • Comparator drug sourcing
  • Long-term storage coordination
Sample Logistics

Biological sample return transport

Reverse logistics are just as critical as forward distribution. Biological samples collected at investigator sites must reach central laboratories within strict time and temperature windows to preserve analytical integrity. All sample shipments are transported as UN3373 Biological Substances, Category B, in full compliance with IATA packaging instructions.

UN3373 compliant: All biological sample shipments use triple-packaging systems meeting P650 packaging instruction requirements.

Sample Types We Handle

Blood samples & serum
Tissue biopsies
Biomarker panels
Pharmacokinetic samples
Urine & saliva specimens
DNA/RNA extractions
Regulatory

Clinical trial compliance

Clinical trial logistics operate under some of the most stringent regulatory frameworks in pharmaceutical distribution. Every shipment must satisfy ICH-GCP guidelines, EU Annex 13 requirements for investigational medicinal products, and GDP standards for temperature-controlled transport. Our processes are designed to meet these overlapping obligations seamlessly, providing sponsors and CROs with audit-ready documentation at every stage.

Compliance Framework

ICH-GCP (Good Clinical Practice) adherence
EU Annex 13 IMP handling requirements
GDP-compliant transport at all temperatures
IATA dangerous goods (Class 6.2, UN3373)
Data integrity per ALCOA+ principles

Trained personnel: All clinical trial logistics are managed by GDP-trained personnel with specific GCP awareness.

Clinical Logistics

Partner with us for your clinical programme

From Phase I first-in-human to Phase IV post-marketing — we support your trial logistics at every stage.