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Creating and Responding to Clinical RFPs Using Citeline and the new Study Feasibility module- Thursday 15th July 2PM UK (9AM EST)
In this 45 minute session you will learn how to identify countries where clinical trials could be run, view patients/site/month data for trials, benchmark enrollment and timing durations and identify investigators with experience relevant to trials you are looking to run. This session will focus on Citeline's Trialtrove, Trial Timing and Sitetrove service. We will also show the new Study Feasibility module. If you would like to set up additional training sessions for you and your colleagues, please contact us at training@pharma.informa.com.

Jul 15, 2021 09:00 AM in Eastern Time (US and Canada)

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