CONSISTENT, CORRECT & COMPLIANT

Are your recruitment materials presented in a manner that is consistent with maximum patient recruitment and approval by your IRB?

iCONSENT standardizes the delivery of Informed Consent Documents in multilingual text as well as an optional video. Electronic signatures, audit trails, and version control ensure regulatory compliance.

REAL-TIME METRICS

Do you have a real-time measure of the number of patients who are in the consent process, accepted or declined consent?

iCONSENT gives you instant insights into each of these measures at each of your research sites. Determine which sites are effective at following up on pending consents as well as derive trends about effective enrollment strategies across all your sites.

ANSWER PATIENT QUESTIONS ON THE FLY

Eliminate concerns that your research coordinators are not answering protocol questions accurately. Patients can ask a question of the central research management team via interactive response system.
Additionally, you can create a custom glossary for word definitions found inside the consent document.