The Essential Guide To Electronic Informed Consent

By Sandra “SAM” Sather, Quality and Regulatory, TrialConsent, CRF Health

This eBook has been designed as an introduction to Electronic Informed Consent (eConsent) in clinical trials, for those researchers considering making the switch from traditional paper-based processes. It will provide an overview of the features and benefits of this technology and how, by integrating eConsent with existing technologies such as eCOA, researchers can reduce burden for sponsor, site and ethics committee study teams, increase participant compliance and retention, and improve overall study outcomes.