
What Is Clinical Trial Supply Management and Why Is It Critical for Trial Success?
Explore how clinical trial supply management ensures timely, compliant, and efficient delivery of trial supplies.
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Founded in 2017, Quantime World Pvt. Ltd. has grown into a trusted global supplier of IMPs (Investigational Medicinal Products), IPs (Investigational Products), and RLDs (Reference Listed Drugs) for clinical research. With a strong focus on quality and reliability, we have earned market credibility in record time. Our state-of-the-art clinical storage and secondary packaging facility further strengthens our capabilities to support end-to-end clinical trial supply needs.
From drug storage to patient travel, we provide end-to-end clinical trial supply and logistics services that ensure your trials run smoothly and efficiently across the global.
Comprehensive solutions for pharmaceutical supply chain excellence
Early planning to align supply with study timelines.
Clinical trial supply management and global supply chain coordination to prevent shortages and disruptions.
Regulatory navigation for smooth export/import compliance.
Product consistency across regions and trial phases.
Cost and timeline optimization through strategic sourcing partnerships.
Established as a Private Limited Company (2017)
Our Journey Began with Comparator Procurement Excellence (2018)
Commenced Storage, Distribution, Returns, and Destruction Services for Clinical Trial Supplies (2019)
Demonstrated Commitment to Quality through ISO 9001:2015 Certification (2020)
Secured FDA License, Enabling Secondary Packaging and Labelling Services for Clinical Supplies (2021)
Enhanced Infrastructure with a 3,500 sq. ft. Facility Expansion (2022)
Established a Strategic Office in the United States (2022)
Diversified Service Portfolio to Include Patient Travel, Outreach, and Adaptive Logistics (2022)
Trusted by global pharma leaders for seamless clinical supply chain solutions. Join the revolution in pharmaceutical logistics.