Advanced Clinical Trials and Clinical Research

eConsent & Retention Tools

eConsent solutions are revolutionizing the informed consent process by offering participants digital, interactive, and accessible formats. This session explores the design, deployment, and compliance requirements of eConsent systems across diverse populations and trial phases. Attendees will learn about multimedia integration, identity verification, and real-time tracking to improve understanding and documentation. The session also delves into retention tools such as mobile apps, reminder systems, and gamification techniques to maintain long-term engagement. Regulatory considerations from FDA, EMA, and IRBs will be covered, alongside data security and multilingual accessibility. Case studies highlight improved comprehension, reduced dropout rates, and operational efficiency gains. Ideal for sponsors, sites, and technology providers, this session provides actionable insights into leveraging digital consent and retention innovations for more participant-friendly and compliant trials.