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#1 InterConnected Platform for Clinical Trial Execution

Boost Efficiency

Reduce Operational Burden

Configure Modular Workflows

Support Decentralized & Hybrid Trials

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Why Teams Choose Jeeva

01

Flexible Trial Configuration

Configure decentralized, hybrid, and site-based trial workflows through one connected platform.

02

Faster Study Launches & Amendments

Rapidly configure studies, manage amendments, and support evolving protocol requirements.

03

Real-Time Operational Visibility

Monitor trial activity, workflows, and operational insights through centralized dashboards.

04

Modular & Transparent Pricing

Deploy only the workflows and modules needed across your clinical operations.

05

Reduced Operational Burden

Minimize manual coordination and logistical overhead across study execution workflows.

06

Improved Retention & Compliance

Support patient engagement, protocol adherence, and operational consistency across study execution.

Unified Workflows Across Clinical Trials

Jeeva helps sponsors, CROs, and research teams manage decentralized, hybrid, and site-based clinical trials through one connected operational platform.

The platform supports connected workflows across patient engagement, study management, scheduling, communication, monitoring, and AI-assisted operational coordination while reducing manual burden across trial execution.

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Compliance Programs Supported

Flexible Workflows for Decentralized, Hybrid, and Site-Based Trials

Jeeva’s modular InterConnected platform supports configurable workflows across decentralized, hybrid, and site-based clinical trials.

Configure informed consent, screening, assessments, patient-reported outcomes, eVisits, follow-ups, and participant engagement workflows through one connected clinical trial environment.

Benefits

Features of the Jeeva eClinical Platform

eConsent

Enable compliant remote and site-based digital consent workflows.

eCOA / ePRO / eDiaries

Collect patient-reported outcomes digitally across decentralized and hybrid trials.

TrialMagnet

Support participant recruitment, screening, and connected enrollment workflows.

eVisits

Support remote participation through integrated teleVisit and virtual trial workflows.

EDC + IWRS

Capture, manage, and organize clinical trial data through one centralized system.

Patient Engagement Portal

Coordinate patient communication, reminders, and engagement workflows across trials.

Adverse Events & Medication Tracking

Manage adverse event reporting and concomitant medication workflows centrally.

Study Scheduler + CTMS

Coordinate visits, scheduling, protocol workflows, and study operations through one centralized environment.

Benefits

Designed for Modern Clinical Trial Operations

Centralize study operations and clinical workflows through one interconnected platform

Support decentralized, hybrid, and site-based clinical trial execution

Enable remote and in-clinic informed consent experiences

Improve participant comprehension through videos, FAQs, and guided interactions

Configure patient-centric workflows across diverse study requirements

Reduce accessibility and geographic barriers across distributed participant populations

FAQ

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

Ask our chat Agent in the bottom right-hand corner anything about us or our solutions.

What modules are included in Jeeva’s eClinical platform?

Jeeva’s eClinical platform offers a comprehensive suite of modules, including Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), ePRO/eCOA for patient-reported outcomes, electronic informed consent (eConsent), visit scheduler, tele-visit capabilities, recruitment CRM, and advanced analytics. All modules are accessible via open APIs for seamless integration with your existing tools and workflows.

How is data quality enforced in eClinical software?

Jeeva ensures data quality through configurable edit checks, automated query workflows, role-based permissions, and end-to-end audit trails. Our platform enables real-time data validation and traceability, helping you maintain high integrity and compliance throughout your clinical trials.

Can we start with one eClinical module and scale later?

Yes, Jeeva’s eClinical platform is fully modular. You can start with a single module that fits your immediate needs, such as EDC or CTMS, and add more modules or unified solutions as your study portfolio grows, ensuring a flexible and scalable approach.

Does the eClinical platform integrate with EMR/EHR systems?

Absolutely. Jeeva supports standards-based interoperability using HL7/FHIR and robust APIs, enabling secure exchange of patient demographics, lab results, and clinical outcomes with your EMR/EHR systems for a seamless data flow.

How fast can we go live with your eClinical software?

Jeeva offers rapid, cloud-based deployment, allowing most studies to go live within weeks. Actual timelines depend on your study protocol complexity, integrations, and any data migration requirements. Our dedicated onboarding team ensures a smooth and efficient launch process.

What security certifications do you follow in eClinical Cloud software?

Jeeva aligns with industry-leading security standards such as SOC 2 and ISO-style controls. Our platform uses strong encryption for data in transit and at rest, offers single sign-on (SSO) and multi-factor authentication (MFA), and enforces least-privilege access policies to keep your data safe and compliant.