Clinical Trials Supply Solutions
GNH India offers end‑to‑end supply chain management for clinical trials—from first patient in through database lock. We ensure investigational products are manufactured, stored, and delivered under full compliance with ICH‑GCP, FDA, EMA, and local regulations.
Whether you’re running Phase I healthy‑volunteer studies or global Phase III oncology trials, our robust infrastructure and trained specialists guarantee product integrity, temperature control, and on‑time site delivery.
Scope & Capabilities
- Global depot network & multi‑modal transport
- GMP‑certified warehousing with real‑time temperature monitoring
- Blinding, labeling, and kit‑building services
- Adaptive randomization support & direct‑to‑patient shipments
- Regulatory filings for import/export and customs clearance
- 24/7 coordination with emergency resupply options
Our Process
We follow a structured six‑step workflow to minimize risk and ensure compliance:
- Forecast & Planning: Collaborate on dosing schedules, site locations, and kit configurations.
- Labeling & Packaging: Generate compliant labels, assemble blinded kits, and perform QC checks.
- Warehousing: Store at controlled conditions in GMP‑approved facilities with continuous monitoring.
- Distribution: Coordinate temperature‑controlled transport to sites, including IP cold chain management.
- Returns & Destruction: Handle unused IP returns, reconciliation, and certified destruction.
- Reporting & Support: Provide real‑time tracking, deviation management, and regulatory documentation.
Why GNH India?
Partnering with GNH India means choosing a proven CRO‑logistics ally with:
- 20+ years in pharmaceutical logistics
- Global GDP/GMP accreditation
- Dedicated clinical supply chain experts
- Real‑time data & interactive dashboards
- Robust emergency resupply protocols
- Comprehensive regulatory support in India and overseas