With COVID-19 continuing to impact trials, a shift in temperature management processes is accelerating.
TORONTO (PRWEB) November 04, 2020
With COVID-19 continuing to impact trials, a shift in temperature management processes is accelerating. Sponsors are fostering new approaches that significantly benefit patient safety, audit readiness, and reduce drug wastage. For some, decreasing manual paper processes at sites and going digital has resulted in quicker process times. Other supply teams are easing into temperature management automation in shipments with the help of digital loggers.
The continuing decentralization of trials also has sponsors looking to integrate temperature management into direct to patient shipments. Drug supply managers who are early adopters in temperature management are learning better organize clinical studies around an increasingly digital cold chain.
Join Henk Dieteren, Clinical Supply Chain Solutions Consultant, Suvoda as he moderates a panel discussion with Mary Pat Walsh, Associate Director, Clinical Supplies, Endo Pharmaceuticals; Ayelet Weissbach, Clinical Supply Chain Manager, NeuroDerm; and Harald van Weeren, Segment Manager Clinical Trials, Berlinger & Co. AG in a live webinar on Wednesday, November 18, 2020 at 9am EST (2pm GMT/UK) where they will answer these questions and more.
For more information or to register for this event, visit Panel: The Future of Managing Cold Chain Supply in Clinical Trials.
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