Our licensed facilities store and distribute controlled substances and hazardous materials, supported by secure, regulatory-approved vaults, rigorous security protocols and monitoring, and full compliance with international dangerous goods handling requirements.

We offer flexible, compliant, and fully documented returns management services to support the complete lifecycle of clinical trial materials. Our processes ensure accuracy, transparency, and audit readiness.

Returned materials are reconciled at three levels, depending on study design and regulatory requirements, ranging from shipper-only counts to verification of contents against packing lists, through to complete unit-level reconciliation of individual tablets, capsules, or vials.

Final destruction is performed by authorized providers, with options for witnessed destruction of controlled substances. Clients receive detailed Certificates of Destruction to support audits and maintain full compliance.

Our storage, distribution, and returns services are built around personalized support that aligns with the specific needs of each clinical study. With dedicated project teams and global logistics experts, we provide the operational insight and hands-on partnership required to manage complex supply chains with confidence. Our proven experience across a wide range of therapeutic areas and trial designs ensures reliable performance, while our end-to-end accountability, from initial storage through final destruction, delivers the assurance and transparency essential for successful clinical execution.