
Pharmaceutical & Medical
Ultra-secure cargo transport for pharmaceutical and medical industry. GDP compliant, temperature-controlled -80°C to +25°C, complete real-time traceability.
Typical use cases
Technical specifications
- Temperature controlled: -80°C to +25°C
- GDP compliant (Good Distribution Practice)
- Full traceability (real-time data logger)
- Temperature validation every 30 seconds
- Certified pharmaceutical insulated containers
- Complete documentation (CMR, health certificates, CoA)
- IQ/OQ qualified packaging (Installation/Operational Qualification)
- Staff trained in pharmaceutical product handling
Pricing & Volumes
Main routes
- Paris → Basel, Geneva, Frankfurt European pharma hubs
- London → Zurich, Brussels, Copenhagen Northern Europe medical distribution
- Europe ↔ USA FDA clinical trials
- Europe ↔ Asie API production (active ingredients)
Compatible services
Temperature Controlled
+20-40%Pharmaceutical cold chain -80°C to +30°C with continuous monitoring
Real-Time GPS Tracking
IncludedSecond-by-second GPS traceability with client link sharing
Express Customs
+5-15%Accelerated customs clearance < 2h with specialized aviation broker
Related cargo industries
Frequently Asked Questions
Everything you need to know about our services
What temperature ranges can you maintain during pharmaceutical cargo flights?
Our cargo aircraft are equipped with both passive and active temperature-controlled containers ranging from -80°C to +25°C. Active units such as the Envirotainer RKN e1 (2–8°C range) and RAP e2 (controlled ambient or 2–8°C for large pallets) provide compressor-driven cooling, while passive packaging relies on PCM (Phase Change Material) insulation from providers like va-Q-tec and Skycell. We use calibrated data loggers with real-time monitoring, ensuring GDP (Good Distribution Practice) compliance throughout the entire cold chain. Each shipment receives a full temperature excursion report upon delivery.
Are your pharmaceutical cargo services GDP and GMP compliant?
Yes, all our pharmaceutical air freight operations are fully GDP (Good Distribution Practice) compliant. Our trained handling teams follow GMP-grade protocols, including clean packaging procedures, contamination prevention, and complete chain of custody documentation from origin to destination. For IMP (Investigational Medicinal Product) shipments used in clinical trials, we apply enhanced traceability and chain-of-condition protocols required by CROs (Contract Research Organizations) managing multi-site studies.
How quickly can you arrange an urgent pharmaceutical cargo charter?
We can have a dedicated cargo aircraft airborne within 4-6 hours of your request. For organ transport — where maximum ischemia time dictates a non-negotiable deadline — our emergency protocol reduces this to under 2 hours. Cold ischemia begins the moment the graft is removed from the donor, so every minute saved during transit directly extends viability. For kidneys under hypothermic perfusion, we coordinate with transplant teams to maintain machine perfusion until the last possible moment before loading. Our 24/7 operations team manages everything including overflight permits and customs pre-clearance.
What types of pharmaceutical and medical cargo do you transport?
We handle vaccines, biologics, cell and gene therapies, IMP (Investigational Medicinal Product) shipments for clinical trials managed by CROs, radioactive isotopes for medical imaging, transplant organs and grafts, blood plasma, and medical devices. For organ logistics, we account for maximum ischemia time and coordinate hypothermic perfusion machines when required. Each cargo type receives a tailored handling protocol — including the choice between passive packaging (PCM-based) and active containers (Envirotainer, va-Q-tec, Skycell) — based on its specific temperature sensitivity and transit duration.
How do you ensure security and traceability for pharmaceutical shipments?
Every pharmaceutical shipment benefits from GPS real-time tracking, tamper-evident seals, and a dedicated chain of custody log. We provide continuous visibility through our online platform, and all handlers are security-vetted. For controlled substances, we coordinate with regulatory authorities for proper documentation and escort protocols. GDP-compliant data loggers record temperature at every stage, and our documentation meets the audit requirements of CROs managing multi-center clinical trials across jurisdictions.

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