Clinical Trial Logistics

Commercial Supply Chain
Planning & Execution for CGT

15+ YEARS OF EXPERTISE
IN THE PERSONALIZED
MEDICINE SUPPLY CHAIN

While healthcare logistics is complex for all types of medical shipments – cell and gene therapies (CGT) are particularly challenging, often requiring extreme time and temperature focus to ensure the successful manufacturing or delivery of a personalized therapy. When it comes to the commercialization of your therapy, speed to scale is vital to meet the global demand for treatments from patients expeditiously and efficiently. With proven experience helping the leading innovators in the CGT space design and implement a clinical-to-commercial scale supply chain, QuickSTAT is uniquely qualified to help bring your personalized medicine to market.

  • Expert temperature-controlled logistics for all temperature ranges to meet the critical transit times to ensure the viability of CGT therapies
  • Reusable shipper inventory management system for 15-25ºC, 2-8ºC, -20ºC, and -40ºC reusable shippers or our LN2 inventory, providing real-time status of units to ensure consistent and robust temperature performance
  • End-to-end VIP temperature-controlled packaging and management via our network of strategically located and GDP qualified conditioning facilities for accelerated turn around
  • Robust chain of custody ensuring individual handling of each patient specimen and CGT, providing the highest security and product integrity
  • Chain of identity management via QuickSTAT’s proprietary IT system, QuickOnline
  • In-transit storage (cold room) using GDP principles and best practices as well as access to temperature-controlled vehicles
  • Pre-qualified routing and real-time GPS tracking with automated alerts to avoid potential delays
  • A market-leading online IT platform, QuickOnline, that is easily integrated with orchestration platforms for real-time data such as temperature, location, orientation and light status
Direct-To-Patient Solutions
Case Study

Direct-To-Patient Solutions
for a Rare Disease
Clinical Study

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