Planning, management, and execution of the supply chain that supports clinical trials, ensuring the safe and compliant delivery of investigational medicinal products (IMPs), comparators, lab samples, medical devices, and patient supplies to and from clinical trial sites. Clinical trial logistics is the specialized supply chain backbone of clinical research, managing the movement of drugs, samples, and materials across global sites—always under strict regulatory and temperature controls—to ensure trials run smoothly and compliantly.

Clinical Trial Logistics refers to the planning, coordination, and management of all materials, data, and supplies required to support a clinical trial—from Phase I through Phase IV. It plays a critical role in ensuring that investigational drugs, biological samples, lab kits, and documentation are delivered on time, intact, and in compliance with regulatory standards.

🎯 Goal: Ensure trial integrity, patient safety, and data reliability through secure, timely, and compliant movement of trial materials.

🧰 Core Clinical Trial Logistics Services includes

🚚 Depot & Site Distribution

❄️ Cold Chain Logistics

📦 Clinical Ancillary Supply Management

🔄 Returns of Unused Drugs

🏥 Clinical Equipment Logistics

⭐ Why These Services Matter

⏱️ Reduce delays and deviations

📜 Ensure regulatory compliance

🧑‍⚕️ Improve patient access and retention

🔒 Maintain Data Integrity & Chain-of-Custody

🌍 Enable Global Reach & Support Complex Trial Designs