Skip to main content

Step 3:

eConsent & Enrollment

Smarter. Simpler. Fully Compliant.

ObvioHealth’s eConsent and enrollment tools set clinical trials on the path to success—right from the start. By combining in-house technology, participant-centric design, and seamless integration, we reduce site burden, improve regulatory compliance, and enhance participant understanding and retention.

Book a consultation

Built-In eConsent, Purpose-Built for Clinical Trials

With ObvioGo’s no-code builder and flexible configurations, sponsors can create and deploy consent flows across geographies—without IT support. This empowers study teams to stay agile and in control while adapting easily to evolving protocol or regulatory requirements.

Everything You Need—In One Platform.

ObvioHealth’s eConsent sets trials up for success with flexible sponsor controls, adaptable site workflows, and a patient-friendly experience that improves engagement from the very first interaction.

Empowered Participants

Participants review key study information in short, digestible sections with built-in quizzes to ensure understanding—improving engagement and data quality from the start.

Facilitated Reconsenting

Participants receive instant alerts when a consent form is updated, prompting them to reconsent before continuing—reducing drop-off risk and supporting compliance.

Transparent Version Control

All current and previous ICF versions are stored and accessible via the study app and platform—minimizing admin time and enabling clear documentation trails.

Confident Participants, Cleaner Data

ObvioHealth’s virtual support and in-app training empower participants from the start—driving higher retention and data accuracy by ensuring they’re confident, informed, and fully prepared to meet study expectations.

Real-Time Clinical Support

Study teams can interact with participants in near real-time to answer questions during the eConsent process, boosting confidence and retention.

Training videos for patients and caregivers

In-app tutorials guide participants through responsibilities such as eDiary usage, medication adherence, device setup, and AE reporting—ensuring clarity across diverse populations.

What You Gain with ObvioGo eConsent

ObvioGo eConsent accelerates enrollment with fewer dropouts, lower risk, and a better participant experience. With built-in eSignatures, real-time support, and in-app training, trials enroll faster, retain better, and deliver cleaner data.

Fully Integrated

Consent flows live inside the ObvioGo platform—designed to scale across decentralized and hybrid study models.

Improved Retention

Clear consent materials, human support, and tailored education reduce participant confusion and dropout.

End-to-End Compliance

From first consent to reconsent, every interaction is tracked, secure, and audit-ready.
Go back
Next Step:
Logistics & Device Management

Making Real Impact

eConsent and the FDA: Implications of New Draft Guidance

The FDA and OHRP have released new draft guidance providing recommendations for making the informed consent process as clear and comprehensive as possible for participants. Here's what you need to know.

› Read more