Clear and Seamless eConsent
Set your clinical trial on a path to success—from the start.
Set your clinical trial on a path to success—from the start.
Traditional informed consent processes are burdensome for participants and sites, prone to errors, and lack flexibility when reconsent is necessary.
ObvioHealth’s eConsent is designed to remove friction and support users. With increased flexibility for sponsors, improved adaptability for sites, and an engaging experience for patients, our eConsent sets your clinical trial on the path to success from the start.
Intuitive UX and on demand support make the eConsent process more transparent and increase understanding of study roles, tasks, and responsibilities.
Seamless reconsenting and versioning control allow sponsors to pivot the protocol without having to worry about damaging delays or regulatory audit findings down the line.
Sites can edit and manage documentation virtually in a streamlined workflow—without increased burden or risk of errors and ambiguities.
Participants
We’ve designed our eConsent to encourage engagement from the start, delivering an interactive user experience that meets patients where they are.
Concise summaries of key information facilitate readability.
Sporadic quizzes boost understanding.
Support is accessible to participants with the click of a button on any app screen.
Sponsors
The process of amending a study protocol doesn’t have to be a nightmare. Our flexible eConsent allows sponsors to pivot with peace of mind—with remote editing, patient reconsenting, and document management processes all streamlined in our ObvioGo® platform.
Sites
Sites are busy. Our eConsent module helps to lighten their workload and smooth their workflows.
ICFs can be standardized across sites or individually edited to accommodate site-specific language.
Site staff can seamlessly view, update, and countersign consent documents whenever necessary.
See how our eConsent module has helped to speed enrollment across multiple TAs.
