Clear and Seamless eConsent

Set your clinical trial on a path to success—from the start.

eConsent Designed for Success at Every Touchpoint

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.  

Participants are informed and empowered.

Intuitive UX and our on-demand COACH team make the eConsent process more transparent and increase understanding of study roles, tasks, and responsibilities.

Sponsors can pivot with peace of mind.

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 have greater oversight and control.

Sites can edit and manage documentation virtually in a streamlined workflow—without increased burden or risk of errors and ambiguities.


Informed participants are engaged participants.

We’ve designed our eConsent to encourage engagement from the start, delivering an interactive user experience that meets patients where they are.

Bite-Sized Summaries

Concise summaries of key information facilitate readability.


Sporadic quizzes boost understanding.

COACH (Clinical Oversight And Coordination Hub) Support

Support is accessible to participants with the click of a button on any app screen.


Protocol changes happen. Pivot with peace of mind.

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.

Facilitated Patient Reconsenting

Push notifications inform patients as soon as an updated consent form is ready to sign, avoiding delays.

Transparent and Traceable Version Control

All current and previous ICF documentation is easily accessible to patients, sites, and sponsors via the study app and ObvioGo platform.


Reduce sites’ administrative burden.

Sites are busy. Our eConsent module helps to lighten their workload and smooth their workflows.

Configurable eConsent Options

ICFs can be standardized across sites or individually edited to accommodate site-specific language.

Supports Multi-Party Management

Site staff can seamlessly view, update, and countersign consent documents whenever necessary.

eConsent Efficiency Across 3 Studies

See how our eConsent module has helped to speed enrollment across multiple TAs.

GI Study with a Fortune 500 Company


Participants consented across 48 states in 24 days.


Retention Rate

Dermatology Study


Participants consented in 56 days.


Medication Adherence Rate


Retention Rate

Women’s Health Medical Device Study


Participants consented in 14 weeks.


Retention Rate


ePRO Compliance Rate

ObvioHealth eConsent: A Linchpin for Trial Success

Increase patient engagement and retention with an interactive consenting experience.
Meet trial milestones with streamlined workflows for sites.
Eliminate regulatory findings with seamless document management.