Informed Consent Document collection and monitoring in real-time.
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.
Eliminate concerns that your research coordinators are not answering protocol questions accurately. Patients can ask a question of the central research management team via an interactive response system.
Additionally, you can create a custom glossary for definitions of words found in the consent document.