CRF Health

The Essential Guide to Electronic Informed Consent_FINAL

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Current Informed Consent Landscape eConsent Explained Global Support for eConsent Features and Benefits Supporting Regulatory Compliance Stakeholder Benefits • Sponsors • CROs • Investigators • Ethics Committees • Participants Counting the Cost Integration with eCOA Making the Move 1 4 5 6 13 16 17 18 19 20 21 22 23 25 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. CONTENTS © CRF HEALTH. ALL RIGHTS RESERVED. WWW.CRFHEALTH.COM

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