We work together with our partners to design and manage clinical trials supply chains of varying scales, from smaller regional studies to complex global multi-center ones.

As clinical trials evolve, the demand for comprehensive supply chain management grows.

At Zuellig Pharma, we understand the importance of seamless logistics in the success of your clinical endeavours. With our extensive experience and expertise, we specialise in providing tailored solutions for clinical sourcing on both global and local scales while ensuring compliance with both local regulations and international standards. Our integrated storage and distribution services, as well as localised reverse logistics, ensure efficiency and accountability at every step.

Our commitment to excellence and making healthcare more accessible is evident through our support of over 5,600 clinical trials worldwide.

Zuellig Pharma Clinical Trial Supply Chain

Global Network

Across APAC, Europe and USA
16
Depots
55+
Markets Covered
5,500+
Projects Managed
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Supporting a Seamless Clinical Trial

In providing leading clinical trial supply chain management and logistics services, we deliver optimised and result-proven solutions to mitigate risk in clinical trials while navigating increasingly-complex regulatory compliance standards. Our Clinical Reach Supply Chain model adapts and supports industry transformations to deliver safe and timely clinical product supply to sites and to patients.

  • Unrivalled local depot network and capabilities for central depot or hybrid depot model tailored to your clinical trial needs.
  • End-to-end clinical supply chain solutions to receive, handle, and distribute IMP and ancillaries according to GMP/GCP regulations.
  • Clinical drug sourcing with global reach, providing local or central sourcing of comparators and ancillaries.
  • Central and local secondary packaging solutions that meet GMP standards.
  • Strategic depots with an extensive, sophisticated temperature-controlled infrastructure for ranging storage temperatures.
  • Regional and local project management expertise.

Comprehensive Clinical Trial Supply Chain Management

We offer precision and agility in our clinical trial supply chain suite of services for streamlined and effective clinical trials:

  • Clinical Storage and Distribution
  • Cold Chain Management
  • Global/Local project management
  • Clinical Sourcing
  • Regulatory Insights
  • Secondary Packaging and Relabelling
  • Returns and Destruction
  • Direct-to-Patient
  • Cell and Gene Logistics & Storage

Customised Clinical Trial Supply Support-Depot Network

Our facilities are capable of handling all kinds of products, including dangerous goods, cytotoxic substances, controlled substances, narcotics, antibiotics, GMOs and other highly potent drugs. Different products have different requirements in clinical trials. Our three distinct supply-chain models: central depot, local depot and hybrid ensure we can cater to your specific needs. Each model offers a full range of unique benefits, including tailored cost control and risk-mitigation strategies.

Cold Chain Management

Incorporating global standards and compliant services, including Good Storage and Distribution (GSDP), we deliver best practices in cold chain management to maintain product integrity and mitigate risks across clinical trials supply chain.

It is crucial in healthcare to ensure that drugs, vaccines and other biological products remain within the specified temperature range to maintain effectiveness and safety. We leverage on innovative passive-packing solutions to optimise cold chain management and distribution. 99.9% of our controlled CTM shipments arrive without temperature excursion — a testament to our rigorous processes and quality control.

Clinical Sourcing

Our robust partnerships with manufacturers and wholesalers fortify our capability to manage your clinical supply needs, ensuring drug product safety and on-time delivery. We offer an integrated approach incorporating:

  • Strategic Central and Local Sourcing Solutions
  • Sourcing of Comparator Drug, Ancillaries and Medical Devices
  • Secondary Packaging and Relabelling Solutions
  • Full Pedigree Information and Product Traceability

Our commitment to excellence ensures that every step, from sourcing to delivery, meets the highest international benchmarks for quality and safety. 

Compliance & Quality Management

Achieving international quality in your clinical trial globally isn’t always easy. However, when you choose Zuellig Pharma as your partner, we can make your clinical trial journey easier for you. Our 16 wholly-owned and partner depots are of the highest calibre and certified to international standards.
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