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Reconsidering Trial Design To Ensure Data Capture in the COVID-19 ERA

Reconsidering Trial Design To Ensure Data Capture in the COVID-19 ERA

Wednesday, June 10, 2020 (1:00 PM - 2:00 PM) (EDT)

Description

COVID-19 has forced a reckoning in how we conduct all aspects of our lives, and clinical trials are no exception. Patient safety is the foundational principle of any trial, and suddenly we have a situation where having patients come into clinical sites for their scheduled visits poses a significant risk to their health and well-being. 

Trials are having to rapidly adjust how they are structured and how data is being captured, sometimes in the middle of ongoing studies. This is accelerating conversations that have been ongoing in the industry for years, with the power of shifting study tasks into the safety of the patient’s own home becoming starkly evident. 

This webinar will share Medidata’s perspective on how clinical trials will be affected in the short term, as the industry rapidly attempts to manage the crisis caused by Covid-19, but also the long term view of how the landscape will be changed by the increased use of technology in trials and the move to trial virtualization.

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