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Clinical Supply Symposium
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
A Study of Global Clinical Supply Practices among Investigative Sites
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)
Mary Jo Lamberti, PHD, MA
Director of Sponsored Research, Research Associate Professor, Tufts Center for the Study of Drug Development, United States
A Study of Global Clinical Supply Practices among Investigative Sites
John Burns
Manager, Solutions Engineering, BioClinica, Inc., United States
Drug Shortages in Clinical Trials
Vladimir Shnaydman, PHD, MSC
President, ORBee Consulting, United States
Optimal Planning for Global Clinical Trial Supply
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