Six Tips For The Successful Integration Of Econsent

Electronic informed consent (eConsent) represents a major improvement in the overall participant consenting process in clinical trials for investigation sites, sponsors and IRB/IECs. eConsent offers researchers numerous benefits, including the capability to mitigate regulatory risk, improve study participants’ comprehension, and provide a more efficient way of collecting consent, therefore saving time and money.

One of the major hurdles for sponsors when integrating an eConsent approach within a clinical trial is the ability to efficiently incorporate another technology into the clinical operations quality system. Here, Mika Lindroos from CRF Health, offers his tips for successful integration.