Clinical Supply Logistics Videos
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End To End Capabilities
As clinical trials evolve to serve various populations and drug sponsors aim to reach patients around the world, utilizing an end-to-end supply chain solution is vital to ensure safe storage and distribution.
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Proactive Strategies To Evaluate And Mitigate Clinical Supply Risk
Learn about strategies that can help build an understanding of risk assessment, in addition to how a study’s protocol requirements, packaging specifications, and more must be identified and addressed.
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Essential Up-Front Planning For Your Clinical Trial
Early planning mitigates risk by avoiding stock outs and study delays, minimizing waste with optimized inventory, and forecasting demand to facilitate robust supply planning.
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Clinical Supply Chain Strategies For Building Resilience
Achieving supply chain resilience is crucial, and flexible distribution strategies and ready-to-use depot and logistics networks are instrumental in establishing limitless flexibility and expertise capable of identifying possible risks.
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Cell & Gene Therapy Supply Chain Challenges: Global, Integrated Solutions
Industry experts share insights to help you mitigate supply chain risk and accelerate access to novel cell and gene therapies.
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Commercial Drug Sourcing For Clinical Trials
Learn how the right partner can leverage years of experience, market knowledge, industry relationships, and clinical packaging expertise to develop a sourcing strategy tailored to the needs of each study.
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Impact Of Supplier Choice On APAC Clinical Trial Execution
Choosing the right clinical packaging and supply chain partner to support APAC studies can vary significantly based upon which countries are involved and the types of services required.
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Improving Supply Chain: Accountability, Sustainability, Optimization
Watch as industry experts explore the advancements in drug accountability facilitated through IRT, encompassing innovative methods for managing site variations and sustainable supply chains.
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Real-Time Track And Trace
Examine how data-driven decisions and a reduced burden for sites and participants can help ensure that clinical trial treatments will be delivered on time and in the condition required.