Ebook

eConsent for Modern Clinical Trials

eConsent for Modern Clinical Trials

Pages 10 Pages

This brief explores the growing adoption of remote and electronic consent (eConsent) in clinical trials. It outlines benefits such as improved patient convenience, reduced site burden, better version control, and fewer consent-related deviations. The document also addresses key considerations, including privacy, accessibility, regulatory compliance, and integration with site workflows. IQVIA emphasizes that well-designed eConsent solutions support decentralized and hybrid trials while enhancing patient centricity and operational efficiency.

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