Poorly managed temperature excursions can be detrimental to the success of a clinical trial. In the supply-chain, managing the process for temperature-sensitive products is extremely intricate and time-consuming.
This webinar will cover, in case study format, Grünenthal’s implementation of a new automated receipt process within Suvoda’s interactive response technology (IRT) system.
Learn about the challenges Grünenthal faced when trying to automate the temperature-controlled shipment receipt process. To automate this process, an integration across three systems was needed, which required close collaboration from Suvoda, Catalent, and Berlinger Group. Learn about the approach that Grünenthal and Suvoda took when first implementing this process within the IRT system and how the results of this pilot clinical trial compared studies not using an automated process.
This webinar will be important for sponsors using temperature-sensitive products because they will learn:
- The intricacies of an automated receipt process within the supply chain lifecycle
- How to overcome challenges faced in a multi-system integration
- How Suvoda’s IRT system turned Grünenthal’s 29-day excursion data evaluation into a same day automated process
- Why this process will have an impact on the future of drug development
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