Current Edition

In Pursuit of eConsent: Best Practice Recommendations for Successful Integration

Electronic informed consent (eConsent) solutions have been
introduced in recent years, representing a major advancement in
improving information delivery to study participants in clinical
research. Mika Lindroos, Director of Product Management at
CRF Health and Sandra “SAM” Sather, Regulatory & Quality,
TrialConsent, CRF Health, give details of how the introduction of
eConsent will represent a major process change for researchers,
and has the potential to have a significant positive impact on study