WHITE PAPER
eConsent for Complex Clinical Trials
How to deliver highly engaging informed consent for better study outcomes
Feb 16, 2023

In this paper, IQVIA Technologies' experts, Karen Maduschke and Vinita Navadgi highlight how a feature-rich electronic consent platform can simplify complex trial designs by reducing the endless stream of consent forms that add time, costs, and risks to each study. Learn how an expertly designed eConsent platform can support master protocol and novel trial designs while improving patient engagement along the way.

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