Assess Clinical Outcomes with Advanced Data-Driven Insights

Assess Clinical Outcomes with Advanced Data-Driven Insights

Jeeva’s eCOA software allows patient-centric data collection by removing distance and language barriers for clinical trial participants. The patients or observers can securely report multilingual outcomes from their devices remotely from their own device (BYOD).

Our eCOA solution enhances patient engagement and enables researchers with multimedia-enhanced assessments and integrating with controlled vocabularies such as MedDRA providing reliable real-time data directly from the source, thereby boosting compliance and minimizing data loss or inaccuracies.

Accelerate Your Trials with Advanced eCOA Solution

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How our eCOA Platform Works

How our eCOA Platform Works

Secure and Compliant: Experience Our eCOA Software Features

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Client Testimonials

Client Testimonials

We Hear You Loud and Clear! Clearing Up Your Jeeva Concerns

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Yes. Jeeva’s eCOA/ePRO platform fully supports “Bring Your Own Device” (BYOD) deployment, allowing participants to use their own smartphones or tablets for reporting outcomes. We also offer provisioned devices for participants who need them, ensuring maximum accessibility and flexibility across diverse patient populations.

Absolutely. Jeeva seamlessly integrates licensed and validated Clinical Outcome Assessments (COAs), manages all necessary permissions, and ensures each instrument version is properly controlled. This facilitates compliance and reliability in both global and local studies.

Our platform supports offline data capture, so patients can complete assessments even without internet access. Responses are securely stored on the device and automatically synced with the study database once the device reconnects, minimizing data loss risk and maintaining study continuity.

Jeeva employs adaptive reminders, delivered via SMS, email, and in-app notifications, that are intelligently timed to patients’ visit windows and local time zones. This personalized approach reduces the likelihood of missed entries and improves data completeness.

Yes. Jeeva’s software supports comprehensive electronic diaries, clinician-reported outcomes (ClinRO), and caregiver workflows. Each role is enabled with tailored, role-based access to streamline workflow, ensure data privacy, and enhance study flexibility.

Yes. Jeeva’s real-time compliance dashboards give study teams instant visibility into data completion rates, timeliness of responses, and identification of outlier data, enabling proactive follow-up and rapid intervention when needed.

Still Curious If Electronic Clinical Outcomes Assessment (eCOA) is a Good Fit for Your Study?

Jeeva eClinical Cloud is designed to be disease-agnostic, device-agnostic, flexible, and modular to support patient-preferred decentralized or hybrid trial operations. Schedule a 30-minute call today to determine the fit. We will help you identify gaps in technology or protocol complexity to enable an informed decision.