Zuellig Pharma
Clinical Trial Support Innovation Center
Zuellig Pharma's Challenges
As clinical trials are becoming increasingly complex, global, and data-driven, Zuellig Pharma faced mounting operational challenges that traditional warehouse models could no longer address:
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Growing efficiency demands driven by rising volumes and greater diversity of clinical materials, requiring faster processing without compromising control or quality
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Multi-temperature operations across ambient, cold, frozen, and ultra-low environments, especially critical for fragile and temperature-sensitive therapies
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High expectations for accuracy and traceability, with every clinical item requiring precise handling, real-time visibility, and full end-to-end tracking
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Stringent GxP compliance requirements, demanding consistently reliable operations and audit-ready processes across all workflows
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Space and energy efficiency constraints, particularly acute in temperature-controlled zones where inefficient layouts increase both costs and risks
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Limited flexibility to adapt to fluctuating trial demands, changing product profiles, and evolving storage requirements
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Sustainability goals, including reducing waste, spoilage, and excess packaging
Our Solution
To address these challenges, Zuellig Pharma implemented Hai Robotics’ HaiPick System 1 at its CTS Innovation Center to support end-to-end clinical trial logistics across both ambient and cold environments. The solution was designed to enhance operational efficiency, accuracy, and flexibility while meeting strict GxP requirements across multi-temperature operations.
The deployment included:
Facility Area: 3,800 ㎡
Shelving Height: 7,350 mm, enabling high-density vertical storage
Robots: 4 HaiPick A42T ACRs (2 serving the ambient zone and 2 serving the cold zone)
Workstations: 2 inbound workstations and 2 outbound workstations
Storage Capacity: 6,500 storage locations across ambient and cold zones
Through this implementation, Zuellig Pharma established a scalable and highly controlled logistics environment capable of efficiently handling diverse clinical materials with precision, speed, and reliability.
What Zuellig Pharma Gained
With HaiPick System 1 in place, Zuellig Pharma Korea has significantly elevated the performance of its clinical trial logistics operations. Here is what the company gained:
- Higher operational efficiency to support growing demand.
Automated storage and retrieval streamlined inbound and outbound workflows, allowing Zuellig Pharma to manage increasing volumes of clinical materials with faster turnaround times and consistent performance.
- Reliable multi-temperature handling across critical zones.
Seamless operations in both ambient and cold environments ensured that temperature-sensitive and high-value clinical materials were stored and fulfilled with the required stability, care, and control.
- Improved accuracy and full traceability under strict GxP requirements.
Real-time inventory visibility and precise item-level tracking reduced errors, minimized expired materials and unnecessary returns, and ensured audit-ready processes at all times.
- Optimized space and energy utilization in temperature-controlled environments.
High-density vertical storage maximized capacity within a limited footprint while lowering energy consumption per unit stored, an especially critical advantage for cold storage operations.
- Greater flexibility to support complex and evolving clinical trials. The scalable system accommodates fluctuating trial volumes and diverse product profiles, with a flexible architecture that allows capacity and throughput to expand in line with Zuellig Pharma’s future growth needs.
With the launch of our CTS Innovation Center and the integration of intelligent automation, we are strengthening our ability to support both domestic and global clinical studies. This solution enables us to manage clinical trial materials with greater accuracy and efficiency, while ensuring they are delivered to patients faster and more reliably.
With the launch of our CTS Innovation Center and the integration of intelligent automation, we are strengthening our ability to support both domestic and global clinical studies. This solution enables us to manage clinical trial materials with greater accuracy and efficiency, while ensuring they are delivered to patients faster and more reliably.
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