Healthcare logistics is not simply about moving products — it is about protecting patient safety. CEVA Logistics brings GDP-qualified operations, validated cold chain infrastructure, and deep regulatory expertise to pharmaceutical distribution, medical device logistics, and hospital supply chain management across 160+ countries.
From biologic drugs requiring ultra-cold storage to surgical implants needing sterile handling and consignment management — CEVA's healthcare logistics portfolio covers every product type, temperature range, and regulatory requirement in life sciences.
Temperature-controlled distribution for biologic drugs, vaccines, cell and gene therapies, and clinical trial materials. CEVA's biopharma operations are GDP-qualified, with validated cold chain lanes and complete data logger traceability from origin to patient.
Precision handling and distribution of medical devices, implants, surgical instruments, and diagnostic equipment. Our medical device operations maintain ISO 13485 quality standards and support consignment inventory management for hospitals and surgical centers.
End-to-end hospital supply chain management from central medical stores to ward-level delivery. CEVA reduces stockouts, eliminates waste, and provides hospitals with real-time inventory visibility across all sites and departments.
Unbroken cold chain logistics for temperature-sensitive healthcare products across air, ocean, and road transport. Continuous temperature monitoring, deviation alerts, and excursion management protect product integrity at every step.
CEVA's healthcare operations are built around a comprehensive compliance framework — audited, documented, and continuously improved to meet the evolving requirements of pharmaceutical and medical device regulators worldwide.
All CEVA healthcare distribution operations are GDP-qualified under EU Directive 2013/C 68/01 and equivalent national frameworks, ensuring pharmaceutical products are distributed to the required quality and integrity standards.
Where CEVA's operations include secondary manufacturing activities such as relabeling, repackaging, or controlled temperature storage of active pharmaceutical ingredients, GMP compliance is maintained and regularly audited.
Our medical device logistics operations are ISO 13485 certified, providing documented quality management systems that meet the stringent requirements of medical device manufacturers and regulatory bodies worldwide.
IATA CEIV Pharma certification across our key air freight hubs ensures that temperature-sensitive pharmaceutical air shipments are handled to the highest possible standards at every point in the air supply chain.
CEVA's dedicated clinical trial logistics team manages the complex, time-critical supply chain for Phase I through Phase IV clinical studies — ensuring investigational medicinal products reach sites and patients on time, at temperature, and with full regulatory documentation.
Connect with a CEVA healthcare logistics specialist to discuss your cold chain requirements, compliance needs, and how we can build a distribution network that meets your most critical performance standards.
