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"Breaking the Bottleneck: Why Paper Consent Slows Digital Trials"

Join this live webinar to learn more.

Every clinical journey starts with informed consent — yet many digital studies still rely on paper, creating delays, compliance risks, and frustration for patients and sites.

Join us to explore how unifying eConsent and eCOA eliminates these barriers and delivers a seamless, patient-first experience from day one.

Through real-world examples in complex re-consenting and pediatric studies, you’ll see how a single, connected workflow improves compliance, reduces site burden, and accelerates study timelines.

Walk away with practical strategies to modernize enrollment, meet evolving regulatory expectations, and maximize the ROI of your digital trial investments.

Discover how one unified platform transforms consent into confidence — and enrollment into momentum.

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