Clinical Storage & Logistics
Secure, Global Clinical Storage &
Cold-Chain Logistics Solutions
Experic delivers cGMP-compliant clinical storage, DEA vault handling, and global cold-chain distribution, ensuring strict investigational product integrity from Controlled Room Temperature (15°C to 25°C) down to Ultra-Low Frozen (-86°C to -50°C) across international Direct-to-Site and Direct-to-Patient (DtP) networks.
cGMP Clinical Storage & Temperature-Controlled Cold-Chain Management
Experic provides strictly monitored, GMP-compliant clinical storage featuring fully validated environments ranging from 15°C to -86°C, supported by automated backup power, redundant HVAC systems, and continuous real-time telemetry to optimize product integrity.
Our facilities in Cranbury, NJ (USA) and Kilbeggan, Co. Westmeath (Ireland) utilize rigorous environmental monitoring to safeguard sensitive biologics and advanced therapies.
Validated Storage Temperature Zones Matrix
| Storage Modality | Validated Temperature Band | Supporting Technologies & Infrastructure | |
|---|---|---|---|
 | Controlled Room Temp (CRT) | 15°C to 25°C |
|
 | Refrigerated / Cold-Chain | 2°C to 8°C |
|
 | Frozen Therapies | -25°C to -15°C |
|
 | Ultra-Low Temp (ULT) | -86°C to -50°C |
|
Schedule II–V Controlled Substance Depot Storage & DEA Compliance
Experic maintains strict 21 CFR regulatory compliance through highly secure, DEA-approved vault and cage facilities, enabling turnkey receipt, storage, and distribution of Schedule II, III, IV, and V investigational medicinal products (IMPs).
Security is integrated into every layer of our controlled drug substance operations to prevent diversion and ensure total trial accountability.
- Strict adherence to DEA regulations and 21 CFR Part 1300 compliance
- Authorized to store and distribute Schedule II–V controlled substances
- High-security, access-controlled DEA-compliant vault and secure cage environments
- Dual-person biometric verification, 24/7 video monitoring, strict electronic chain of custody
Global Clinical Supply Chain Distribution & Import/Export Management
Operating strategically from US and EU depot hubs, Experic orchestrates seamless transatlantic global distribution, supported by comprehensive customs clearance, duty management, and EU/UK Qualified Person (QP) release coordination.
Whether routing investigational supplies to localized clinics or managing complex international trials, Experic leverages validated lanes for both Direct-to-Site and Direct-to-Patient (DtP) shipping protocols.
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Powered refrigerated containers providing continuous active temperature regulation
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Validated Phase Change Materials (PCM) and Liquid Nitrogen (LN2) vapor dry shippers
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Real-time telemetry tracking of temperature, humidity, tilt, and GPS location
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Compliant Direct-to-Site and Direct-to-Patient (DtP) global delivery via validated couriers
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US Manufacturing Facility
2 Clarke Drive, Cranbury, NJ 08512
888.397.9733 (toll-free)
609.537.4040
info@expericservices.com -
Analytical Lab
One Duncan Drive, Cranbury, NJ 08512
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EU Depot
Experic Ireland LTD,
Unit 7, Midlands Gateway Business Park, Kilbeggan,
Co. Westmeath.
Lifecycle & Returns Operations
Experic ensures lot-level batch traceability and full lifecycle management of clinical supplies via real-time inventory tracking, offering expiry date extensions, language translation over-labeling, and secure, cGMP-compliant reconciliation and destruction.
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Integrated tracking software provides total visibility into lot status, supply consumption, and individual temperature histories from raw material receipt to finished product.
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Comprehensive services for language translation, re-labeling, and compliant expiry date extensions to maximize usable clinical inventory.
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Secure IMP receipt, line-item reconciliation, quarantine handling, and environmentally certified, cGMP-compliant destruction of unused or expired trial materials.
Expansion & Future Growth
Our facility continues to grow. With over 20,000 square feet of undeveloped space, we’re building towards even greater capacity, allowing us to meet both clinical and commercial-scale demands with ease.
Frequently Asked Questions
Clinical Storage & Logistics
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Experic provides cGMP-compliant clinical storage and global logistics for investigational medicinal products (IMPs), including controlled room temperature, refrigerated, frozen, and ultra-low temperature storage. Services also include controlled substance handling, global distribution, Direct-to-Site and Direct-to-Patient (DtP) delivery, inventory management, returns, reconciliation, and destruction.
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Experic provides validated clinical storage environments ranging from Controlled Room Temperature (15°C to 25°C) down to Ultra-Low Frozen (-86°C to -50°C). Capabilities include refrigerated storage at 2°C to 8°C and frozen storage at -25°C to -15°C, supported by continuous environmental monitoring and backup systems.
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Yes. Experic supports the secure receipt, storage, and distribution of Schedule II–V controlled substances using DEA-compliant vault and cage environments. Controlled substance operations incorporate restricted access, continuous monitoring, electronic chain-of-custody controls, and procedures designed to maintain clinical trial accountability.
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Yes. Experic supports global clinical trial distribution through clinical supply hubs in Cranbury, New Jersey, and Kilbeggan, Ireland. Capabilities include validated cold-chain shipping, customs and import/export management, EU/UK QP release coordination, and Direct-to-Site and Direct-to-Patient delivery.
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Experic provides lifecycle management of clinical supplies through real-time inventory tracking, lot-level traceability, expiry date extensions, over-labeling, returns management, reconciliation, quarantine handling, and cGMP-compliant destruction of unused or expired investigational products.