Where clinical trial expertise meets supply chain excellence
Global forces from every direction are amplifying the complexity of clinical trial logistics. Changing regulations across regions, country-specific requirements, geopolitical factors, tariffs, and intensifying financial pressures intersect with the growing intricacy of clinical studies.
At Parexel, our operations are designed to manage this complexity – with a single point of contact for our customers across all trial logistics moving to or from the site and/or sponsor. Whether you are conducting a small regional project or a complex global trial, you need a robust supply chain network that includes country-specific knowledge and a close connection to local authorities.
We offer an extended chain of custody from protocol to patient and back, maintaining accountability while minimizing risk and accelerating timelines. We follow the drug and sample until the study is complete and the drug is brought back for destruction. We provide end-to-end solutions or can fill gaps in coverage with targeted expertise on a standalone basis. These capabilities extend to global trade compliance and importer of record (IOR) and exporter of record (EOR) services.
A global CRO with world-class clinical logistics capabilities
Parexel Clinical Logistics is where clinical trial, regulatory, and logistics expertise meet. We offer integrated regulatory expertise, quality management, clinical trial execution, lab and sample management, drug supply, and ancillaries and medical devices, all under one roof. When clinical trial and logistics operations work together, processes are simplified, streamlined, and accelerated. Technology integrations are prebuilt. Handoffs are eliminated. Project management enables the convergence of GCP and GMP.
Patients and sites: always our central focus
Our goal is to ensure that clinical trial patients receive the right treatment, on time, every time, and safely. Our integrated services include:
- Clinical trials supply
- Ancillary and device management
- Lab logistics services
- Global trade compliance
The intersection of technology, expertise, and global and local knowledge
When participants are generous enough to provide biological samples for a study, we are responsible for handling them with care and caution. For example, we tie informed consent to samples collected for future biomedical use in the sample tracking software, ensuring that sponsors down the road can easily determine where samples are and what can be done with them. With integrated locations worldwide, our approach is flexible and scalable. We can help with:
- Improved inventory control for all types of human biological samples starting at time of collection
- Consolidation of purchasing, storage, assembly, and transportation processes
- Common-sense shipping solutions to reduce the overall number of shipments, costs, and ultimately our carbon footprint
- Accurate supply forecasts, as well as sophisticated reporting on expiry dates and shipment status
- Country-by-country knowledge of import/export rules, avoiding complications such as bans on certain diagnostic and testing equipment
- Testing capabilities using our chain of lab partners
Strategically located depots across the globe
We reach sites and patients, wherever your trial is. Through our global network, Parexel can:
- Provide local or central sourcing of comparator and non-investigational medicinal products
- Coordinate investigational medicinal products (IMP) manufacturing to optimize material utilization, supply and resupply strategies, expiration dates, and costs
- Offer full-service and secondary clinical packaging for randomized, double-blind, or two/three-panel studies, as well as customized packaging design, customized secondary packaging, and patient supply kits
- Develop, translate, and distribute all the documentation for sites, investigators, or patients
- Receive, handle, and distribute IMP and ancillaries according to GMP regulation
Parexel's owned depot locations
Select a location on the map.
CASE STUDY
Leveraging distribution and global trade compliance strategy to create competitive advantage
clinical logistics projects over the past 5 years
dedicated and qualified logistics experts
Our experts
Tony Heeley
Director, Production Services
Vince Santa Maria
Senior Vice President, Clinical Logistics
Jeff Ten
Senior Director, Supply and Logistics
Diana Cristina Pelaez Valencia
Associate Director, Supply & Logistics Portfolio Management
Christian Consoli
Director of Supply & Logistics, Laboratory Services
Daniela Martinez
Associate Director, Global Trade Compliance
Stacey Stentiford
Associate Director, Supply and Logistics
Sanjay Vyas
President of Patient Safety Services & Clinical Logistics and Managing Director of India
Laurie McRae
VP, Solution Consulting & Account Management - Safety and Logistics
Alberto Quintero
Executive Director, Supply & Logistics, PLD Packaging, Labeling & Distribution
Our experts
Tony Heeley
Director, Production Services
Vince Santa Maria
Senior Vice President, Clinical Logistics
Jeff Ten
Senior Director, Supply and Logistics
Diana Cristina Pelaez Valencia
Associate Director, Supply & Logistics Portfolio Management
Christian Consoli
Director of Supply & Logistics, Laboratory Services
Daniela Martinez
Associate Director, Global Trade Compliance
Stacey Stentiford
Associate Director, Supply and Logistics
Sanjay Vyas
President of Patient Safety Services & Clinical Logistics and Managing Director of India
Laurie McRae
VP, Solution Consulting & Account Management - Safety and Logistics
Alberto Quintero
Executive Director, Supply & Logistics, PLD Packaging, Labeling & Distribution
Learn more
Video
Parexel Clinical Logistics: Asia-Pacific Distribution Center
Jul 6, 2026
Video
Parexel Clinical Logistics: North America Distribution Center
Jul 6, 2026
Video
Parexel Clinical Logistics: Europe Distribution Center
Jul 6, 2026
Blog
Delivering GxP: A holistic approach to clinical logistics
Apr 7, 2026
Playbook
Delivering radiopharmaceutical trials through integrated clinical expertise
Mar 11, 2026


