Seamless Planning, Sourcing, and Delivery of Clinical Trial Materials – Globally Compliant, Patient-Focused
At Pharm Edge Global, we provide comprehensive Clinical Trial Supply Management services that ensure the right product reaches the right site at the right time—without delays, disruptions, or deviations. Whether you’re a pharmaceutical company, biotech startup, or Contract Research Organization (CRO), we handle every step of the clinical supply chain with precision, compliance, and care.
Our end-to-end solution covers the full lifecycle of your study—from supply planning and forecasting to sourcing, packaging, storage, global distribution, and returns & destruction. We support both Phase I–IV trials and multi-country studies, meeting strict regulatory standards across the globe.
✅ Our Clinical Trial Supply Services Include:
- Clinical Supply Strategy & Forecasting
Efficient planning based on study design, patient enrollment rate, and site demand to prevent overstocking or stock-outs. - Sourcing of Investigational & Comparator Drugs
Procurement of IMP (Investigational Medicinal Products), placebos, reference drugs, and ancillary supplies through approved, validated vendors. - Clinical Packaging & Labeling
GMP-certified blinding, labeling, and packaging services compliant with ICH-GCP, USFDA, EMA, and country-specific regulations. - Cold Chain & Ambient Storage
Secure storage solutions in 2–8°C, -20°C, -80°C, and controlled room temperature environments at GDP-compliant facilities. - Global Distribution to Study Sites
Timely delivery of clinical trial materials to domestic and international trial sites, with real-time tracking and temperature monitoring. - Returns, Reconciliation & Destruction
Full chain of custody for used, unused, and expired supplies, including compliant returns management and certified destruction.
🌍 Clinical Trial Supply Management for:
- Oncology
- Neurology & Rare Diseases
- Infectious Diseases (HIV, COVID-19, Hepatitis)
- Cardiology & Endocrinology
- Vaccine Trials
- Biosimilars & Biologics
🛠️ Additional Support Services:
- Randomization & IWRS/IVRS Integration
- Depot Network Management
- Custom Kit Assembly
- Quality Assurance & Audit Readiness
- Documentation & Regulatory Filing Assistance
👥 Who We Work With:
- Global & Regional CROs
- Pharmaceutical & Biotech Companies
- Research Hospitals & Academic Institutions
- Government Trial Sponsors
- Investigator-Initiated Trials (IITs)
🔐 Why Choose Us?
- GMP, GDP, GCP, and ISO 9001 Certified Partners
- Expertise in multi-country & multi-phase clinical trials
- Proven capability in temperature-sensitive shipments
- Rapid, flexible, and responsive trial supply support
- Transparent pricing, robust compliance, and expert coordination
💬 On-Time, Every Time – Because Every Patient Counts
In clinical trials, logistics failure is not an option. Our clinical trial supply management solutions are built around efficiency, reliability, and regulatory precision, ensuring your study runs smoothly from first patient to last dose.
👉 Contact us today to discuss your clinical supply requirements or request a custom proposal from our clinical logistics team.