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.

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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.

Selección y validación de instrumentos

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.

Seleccione los instrumentos óptimos

Identificamos los instrumentos, dispositivos y dispositivos portátiles que son más apropiados para la población, la afección y el tratamiento en estudio.

Evalúe las ventajas y desventajas

Arbitramos entre la reducción de la carga de los pacientes y la calidad de los resultados, teniendo en cuenta la fatiga, la usabilidad y la granularidad de los datos.

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.