Shipexworld provides GDP-compliant pharmaceutical air freight from India to global healthcare providers, research institutions, and pharmacies, ensuring temperature-controlled delivery of life-saving medications, clinical trial materials, and medical supplies. Our specialized pharma logistics maintain strict regulatory compliance and cold chain integrity across all major pharmaceutical corridors.
Pharmaceutical exports from India serve hospitals, research labs, and pharmacies worldwide, requiring absolute precision in temperature management and documentation. Shipexworld handles temperature-sensitive vaccines, biologics, oncology drugs, and clinical trial shipments with real-time monitoring and unbroken cold chain protocols. We coordinate from GMP-certified facilities in Hyderabad, Bangalore, and Mumbai to destination hospitals, pharmacies, and research centers globally
Our service covers both commercial pharma volumes and urgent single-dose shipments, with dedicated pharma handling staff trained to IATA temperature control regulations and WHO GDP standards. Healthcare providers trust our proven compliance record across FDA, EMA, MHRA, and CDSCO requirements.
Controlled Room Temperature (CRT) 15-25°C
Most oral solid dosages, tablets, capsules
Standard pharma packaging acceptable
Real-time temperature monitoring
Data loggers with 15-minute intervals
Cold Chain 2-8°C (Refrigerated)
Vaccines, insulin, certain biologics
Biodegradable gel packs or dry ice
Pre-qualified reefer containers
Continuous temperature validation
Frozen -20°C
Certain biotech products, reference standards
Dry ice shipments (IATA PI 954 compliant)
Specialized insulated containers
Dual temperature monitoring systems
Ultra-Low -70°C to -80°C
mRNA vaccines, gene therapies
Liquid nitrogen vapor shippers
Fully validated ultra-low systems
White glove handling procedures
Primary Pharma Gateways:
Critical Transit Windows:
| Destination | CRT | 2-8°C | Frozen | Ultra-Low |
| USA East Coast | 24h | 20h | 18h | 12h |
| Europe | 18h | 15h | 12h | 10h |
| Singapore | 6h | 5h | 4h | Direct |
| Dubai | 4h | 3h | 3h | 2h |
USA (USFDA):
✓ Facility registration with FDA
✓ Drug establishment registration
✓ Temperature excursion reporting
✓ Import Alert screening clearance
✓ Prior Notice (PN/AIR) filing
Europe (EMA):
✓ GDP certification compliance
✓ Qualified Person (QP) release
✓ EudraGMDP database verification
✓ MAH authorization documentation
✓ Temperature validation records
CDSCO India Export Requirements:
✓ Export NOC from CDSCO portal
✓ CoPP (Certificate of Pharmaceutical Product)
✓ GMP certificate (Schedule M compliant)
✓ Free Sale Certificate where applicable
✓ Manufacturing license verification
Other Markets:
✓ ANVISA (Brazil), PMDA (Japan), TGA (Australia)
✓ Health Canada NDS requirements
✓ Saudi SFDA pharma import protocols
✓ South Africa SAHPRA clearance
Comparator drugs from reference labs
Investigational Medicinal Products (IMP)
Ancillary supplies (syringes, kits)
Bio-samples (blood, plasma, tissue)
Chemotherapy medications (<24h worldwide)
Transplant medications (emergency STAT)
Rare disease treatments (orphan drugs)
Compassionate use shipments
Chain of Custody: Dual-signature protocols, tamper-evident seals, dedicated pharma flights when available.
Temperature Mapping: Pre-shipment qualification of packaging
GMP Verification: Source facility compliance confirmation
Qualified Packing: IATA-compliant thermal packaging assembly
Temperature Validation: Data logger activation and testing
Regulatory Documentation: CDSCO NOC, CoPP, import licenses
Priority Airport Handling: Pharma priority screening lanes
Flight Assignment: Temperature-controlled aircraft allocation
Continuous Monitoring: GPS + temperature telemetry
Destination Cold Chain: Direct transfer to pharma warehouse
QP Release (Europe): Qualified Person final validation
Portal Access: Live temperature graphs, customs status, QP handover confirmation.
✅ GDP Certification: Full Good Distribution Practice compliance
✅ White Glove Handling: Dedicated pharma-trained staff
✅ Temperature Excursion SOP: Immediate notification + recovery protocol
✅ 24/7 Pharma Helpline: Critical shipment escalation
✅ Regulatory Team: CDSCO/USFDA/EMA specialists on staff
✅ Clinical Trial Expertise: 21 CFR Part 11 compliant tracking
Commercial Pharma:
🇺🇸 USA: New York, Los Angeles, Chicago pharma hubs
🇬🇧 UK: London, Manchester hospital supply
🇩🇪 Germany: Frankfurt, Munich research centers
🇸🇬 Singapore: Regional pharma distribution
🇦🇪 UAE: Dubai healthcare city
Clinical Trial Hubs:
🇺🇸 Boston (Harvard/MGH), San Francisco (UCSF)
🇬🇧 London (Imperial College), Oxford
🇩🇪 Berlin (Charité), Munich (LMU)
🇯🇵 Tokyo (National Cancer Center)
🇦🇺 Sydney (Royal Prince Alfred)
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