In the evolving world of clinical research, storing investigational products has become more than just a matter of cold chain logistics. As trials become increasingly complex and regulatory demands tighten, drug developers seek storage partners who provide space, security, scalability, and strategic support. Enter GMP clinical storage capabilities designed to meet the needs of modern trials with flexibility, speed, and compliance.

The GMP Storage Challenge in Today’s Clinical Trials

Clinical trials today are rarely simple. Sponsors navigate global, multi-site studies with varying regulatory requirements, handle highly sensitive or high-potency compounds, and operate under aggressive development timelines. In this environment, clinical material storage must be more than just a passive warehouse function—an integrated, agile component of trial success.

Temperature excursions, shipping delays, and limited visibility into inventory can introduce serious risks, ranging from product degradation to compliance failures. To mitigate these risks, companies need a partner who stores drug products and actively manages them with precision and foresight.

More Than a Warehouse: Experic’s Purpose-Built Storage Solutions

Experic has redefined GMP clinical storage. Housed within its 73,000-square-foot, purpose-built facility in Cranbury, New Jersey, Experic offers a full spectrum of GMP-compliant storage environments—from ambient and refrigerated to frozen and ultra-low temperature. This range of capabilities ensures that products with even the most sensitive stability profiles are maintained under ideal conditions throughout their lifecycle.

Key facility features include:

  • Temperature-controlled storage for 2–8°C, -20°C, and -80°C environments
  • Real-time environmental monitoring and backup systems to ensure data integrity
  • Controlled substance and DEA-compliant storage for high-potency products
  • Secure chain-of-custody protocols to maintain regulatory traceability

Specialized Support for Complex Products

High-potency compounds and novel formulations require more than just a cold room—they demand a partner experienced in handling complex, often unpredictable materials. Experic’s facility is equipped and staffed to support:

  • Hazardous or cytotoxic materials requiring containment and specialized handling
  • Dry powder inhalation therapies, including electrostatically charged or cohesive powders
  • Custom packaging and labeling needs integrated with storage and distribution

Experic’s GMP clinical storage capabilities are designed to adapt whether your trial involves temperature-sensitive biologics or niche solid-dose formulations.

Storage Built for Agility and Growth

Speed and scalability are often the defining factors in trial success. With rapid trial startups and mid-study changes becoming the norm, storage providers must be able to pivot fast. Experic is uniquely positioned to support:

  • Fast onboarding for new studies, with minimal red tape
  • Flexible storage volumes, from early-phase clinical batches to commercial-scale shipments
  • Integrated inventory management with clear visibility, reconciliation, and return handling

This agility means that initiating a Phase 1 trial or scaling a late-phase global study will give you the storage infrastructure you need without unnecessary delays or bottlenecks.

Integrated with Full Clinical Supply Services

What sets Experic apart isn’t just the quality of its storage—it’s the seamless integration with the rest of the clinical supply chain. As a full-service CDMO, Experic connects its storage services directly to:

This end-to-end service model reduces risk, simplifies coordination, and accelerates timelines by consolidating essential functions under one roof. Fewer handoffs mean fewer opportunities for error and a smoother path from production to patient.

Why Sponsors Trust Experic

Experic is more than a vendor—it’s a partner. Clients rely on Experic’s collaborative approach, backed by experienced project managers and responsive teams. Every storage solution is customized to each trial’s unique needs, and sponsors are encouraged to work side-by-side with Experic experts on-site when needed.

With a reputation built on experience, expertise, and expedited service, Experic consistently earns the trust of sponsors conducting the most demanding trials.

GMP Clinical Storage That Moves Your Trial Forward

In today’s clinical environment, storage isn’t a back-end function—it’s a frontline service that protects your assets, supports your timelines, and upholds your regulatory commitments. Experic’s GMP clinical storage capabilities go beyond the freezer to offer tailored, agile solutions that grow with your trial.

Partner with Experic to ensure your clinical materials are handled with the care, compliance, and precision they deserve—every step of the way.