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Session Chair(s)
Mary Jo Lamberti, PHD, MA
Director of Sponsored Research, Research Associate Professor
Tufts Center for the Study of Drug Development, United States
Learning Objective : Discuss some of the key challenges that investigative sites encounter in the management of clinical supplies; Describe different approaches to clinical supply planning including the application of developed technologies; Discuss effective drug supply strategies and ways to address drug shortages.
Speaker(s)
A Study of Global Clinical Supply Practices among Investigative Sites
Mary Jo Lamberti, PHD, MA
Tufts Center for the Study of Drug Development, United States
Director of Sponsored Research, Research Associate Professor
Drug Shortages in Clinical Trials
John Burns
BioClinica, Inc., United States
Manager, Solutions Engineering
Optimal Planning for Global Clinical Trial Supply
Vladimir Shnaydman, PHD, MSC
ORBee Consulting, United States
President
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