Quantime World Pvt. Ltd. was founded in 2017 and is headquartered at Shivshakti Complex, Wagholi, Pune, Maharashtra, India. The company has grown from its founding focus on comparator drug procurement into a full-service clinical trial supply chain organisation, establishing an operational footprint across India, the United States (Lewes, Delaware), Singapore, and Bulgaria (Sofia) — the latter providing a European Union-based entity for EU market operations.

The company’s growth trajectory reflects a structured capability build-out: comparator procurement from inception in 2018, storage and distribution services from 2019, ISO 9001:2015 certification in 2020, FDA licence and secondary packaging capability in 2021, a 3,500 sq. ft. facility expansion in 2022, a US office established in the same year, and a service portfolio expansion into patient travel and home healthcare also in 2022. Its clinical storage and secondary packaging facility is GDP-compliant with temperature-controlled infrastructure and 24/7 real-time monitoring.

Quantime World’s primary client base comprises pharmaceutical and biotechnology sponsors and CROs conducting multi-country clinical trials, for whom it provides a single-source clinical supply chain partner across storage, packaging, distribution, logistics, and patient support. The company’s global depot partner network extends its distribution reach across more than 50 countries without requiring owned infrastructure in each market.

Key Products and Services

Drug Storage and Distribution

• GxP- and GDP-compliant storage of investigational medicinal products (IMPs), investigational products (IPs), and reference listed drugs (RLDs) in temperature-controlled conditions spanning ambient, refrigerated (2–8°C), and frozen environments
• 24/7 real-time temperature monitoring, security, and compliance tracking
• Distribution of clinical trial materials to investigator sites across global markets via owned and partner depot network

Blinding, Repackaging and Labelling

• Secondary packaging and over-encapsulation services for blinding of investigational products
• Country-specific compliant labelling incorporating barcoding and tracking systems aligned with local regulatory requirements
• FDA-licensed packaging facility supporting regulated market requirements

Comparator Drug Procurement

• Global sourcing and procurement of comparator drugs and reference products from authorised suppliers
• Full chain-of-custody documentation and traceability from procurement through to site delivery
• Strategic sourcing partnerships to optimise cost and availability across multiple markets

Clinical Trial Supply Logistics

• End-to-end logistics management for clinical trial materials, including last-mile delivery to investigator sites
• Temperature-controlled transport solutions for ambient, cold chain, and frozen shipments
• Export and import compliance management, customs clearance, and regulatory documentation for cross-border shipments

Biosample Logistics

• Specialist handling and logistics for biological samples including tissue, blood, and other biospecimens
• Temperature-controlled chain-of-custody tracking and regulatory compliance for international biosample export

IRT (Interactive Response Technology) Services

• IRT system implementation and management for patient randomisation, trial supply chain optimisation, and real-time data management within clinical trials

Return and Destruction Services

• Secure return logistics for unused, expired, or recalled clinical trial materials
• Compliant destruction services with full documentation and audit trail generation

Document Archival Services

• Physical and digital archival of clinical trial documentation and regulatory records
• Secure, compliant document storage aligned with GCP retention requirements

Home Healthcare Services

• Specialist home healthcare services enabling clinical trial treatments to be administered in patients’ homes, supporting decentralised and hybrid trial models
• Professional coordination of home visits, treatment administration, and patient safety monitoring

Patient Travel Services

• Full-service travel coordination for clinical trial participants, including transportation, accommodation, and logistical support
• Patient reimbursement and travel expense management

Global Project Management

• Dedicated project management spanning all clinical supply chain activities across multi-country studies
• Early planning, regulatory navigation, supply chain coordination, and cost and timeline optimisation

Quantime World occupies a practical niche in the clinical trial supply chain market as an India-headquartered, globally operational clinical supply organisation that has built its service portfolio systematically since 2017, progressing from a comparator procurement focus to a comprehensive end-to-end supply chain offering within seven years. Its combination of Indian operational cost efficiencies, an FDA-licensed packaging facility, ISO 9001:2015 certification, and a growing international office network — spanning the US, Singapore, and an EU entity in Bulgaria — positions it as a credible clinical supply partner for sponsors running multi-regional studies that require cost-competitive, GDP-compliant supply chain management. The addition of home healthcare and patient travel services reflects alignment with the industry’s growing interest in decentralised and hybrid clinical trial models, where patient-centric logistics are increasingly relevant. Relative to established global clinical supply organisations such as Almac, Catalent Clinical Supply Services, and Marken, Quantime World is a younger, smaller, and still-scaling organisation, but its structured capability expansion and multi-continent presence indicate a deliberate growth trajectory.