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
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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
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