Personalization
Personalized service, tailored to the specific needs and requirements of your study.
Our world-class infrastructure includes GMP-compliant storage facilities, specialized handling for controlled substances and dangerous goods, and comprehensive returns and destruction management.
With global reach, regulatory compliance, and complete accountability at the center of our operations, we bring more than 30 years of experience to the storage, distribution, and returns management of clinical trial materials. Having supported thousands of studies across 100+ countries, we deliver tailored, dependable solutions for projects of all sizes and complexity.
Our secure, GMP-compliant facilities are purpose-built for investigational medicinal products and maintained to the highest Good Manufacturing Practice standards. We ensure optimal storage conditions via 24/7 environmental monitoring, advanced access control and surveillance systems, and temperature-controlled zones tailored to a wide range of product requirements.
Our global logistics network is managed by experienced clinical supply chain experts who oversee end-to-end distribution of patient kits worldwide. They ensure every shipment is delivered safely, securely, and on time through international shipping across all regions, integrated cold chain and ambient solutions, and comprehensive customs compliance and regulatory support.
Our controlled and dangerous goods capabilities are delivered through fully licensed and approved facilities equipped to store and ship controlled substances and hazardous materials, supported by secure, regulator-approved vaults, robust security protocols and monitoring, and full compliance with international handling standards.
We provide flexible, compliant solutions for the return, reconciliation, and destruction of clinical trial materials, in accordance with study protocols and regulatory requirements. From a simple shipper count to verification of shipper contents against packing lists to complete unit-level reconciliation of individual tablets, capsules, vials, and other injectable dosage forms we ensure complete accountability with clear documentation at every stage.
Final and secure destruction is carried out by authorized third-party providers, with the option to witness controlled substance destruction. We provide comprehensive Certificates of Destruction (CoD) that ensure full compliance, clear documentation, and complete audit readiness.
Personalized service, tailored to the specific needs and requirements of your study.
Dedicated project teams and logistics experts, providing hands-on oversight and consistent communication.
Proven global experience, supporting diverse therapeutic areas across regions and markets worldwide.
End-to-end accountability, from secure storage through distribution, returns management, and final destruction.
Sterile Clinical Trial Services
Structure in every stage, momentum for every milestone, we bridge science to success with partnership, supporting every step of your product pathway.
Learn more about our sterile capabilities that deliver quality, innovation, and reliability from development through commercialization.
Contact us today to talk to our expert customer services team about how we can support you with pharmaceutical storage & distribution services.