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Clinical Trial Logistics

Clinical trial logistics ensures secure, compliant transport of investigational products, samples, and temperature-sensitive materials across sites, labs, and patients globally

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Clinical Trial Logistics

Pharmalogi is specialise in the development of customised, high-quality medical cold chain management & logistics solutions for clinical trials, providing comprehensive logistical support throughout each phase of development—from preclinical research to the commercialisation of drugs and treatments. Our objective is to minimize the time required for clients to progress their products from the molecular stage to final commercial drug status. We ensure that each shipment is delivered within the designated temperature range and timeframe by implementing optimal care and utilizing appropriate solutions, handled by our highly trained professional team. We place a strong emphasis on preventing shipment mismanagement and take all necessary measures to ensure that our clients do not encounter delays due to temperature deviations, misrouting, or failure to adhere to specific requirements and instructions.

Pharmalogi’s clinical trial logistics expertise spans every phase of drug development—from Phase I-IV studies to decentralized and direct-to-patient models. We manage the end-to-end supply chain for investigational medicinal products (IMPs), diagnostic kits, and biological samples, ensuring temperature-controlled shipments (ambient, refrigerated, frozen, cryogenic) with full chain-of-custody and global regulatory compliance. Each movement—be it depo/pharmacy/sponser/CRO-to-site, site-to-site, site-to-lab, direct-to-patient, or shipment of return medication from sites-to-depo/pharmacy/sponser/CRO—is executed with precision, visibility, and real-time monitoring.

Challenges We Solve For CT

Clinical trials require logistics solutions that go beyond transportation—they demand compliance, speed, and flawless execution. Pharmalogi addresses critical challenges by:

  • Maintaining strict temperature ranges (Ambient(room),+15°C to +25°C,+2 to +8°C,-25°C to -15°C,-80°C to -20°C, LN2)
  • Preventing delays due to customs and improper documentation
  • Each shipment is maintained within a stringent Chain of Custody, as we acknowledge the high research value of every shipment, which renders them irreplaceable.
  • Multi-country coordination and time zone complexities are mitigated through our global network and 24/7 control tower.
  • Ensuring patient-centric, last-mile delivery in most remote or highly regulated areas

With deep domain knowledge and integrated systems, we minimize risks and streamline operations so your clinical trials stay on track.

Our Advantage

Pharmalogi delivers scalable, audit-ready, and globally compliant logistics tailored to each study’s protocol. With 24/7 control tower oversight, site-level training, validated packaging, and proactive contingency plans, we act as an extension of your clinical operations. Our solutions accelerate study timelines, mitigate temperature excursion risks, and deliver confidence from initial site supply to patient bedside.