Learn about how clinical research companies navigate the complexities of sample and IP logistics in the rapidly evolving cell and gene therapy landscape.
Proper logistics management for cell and gene therapies during clinical trials necessitates meticulous planning, execution and oversight. These therapies are exceptionally time- and temperature-sensitive, requiring precise transport and storage conditions. This white paper explores the regulated steps comprising the journey of CGT products, the importance of supply chain efficiency in preventing disruptions, the stringent storage and stability protocols to preserve biological integrity, and our expansive infrastructure to handle the escalating demands and scalability of CGT trials.
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