Simplify Clinical Trial Data Capture and Management with Jeeva EDC

Unified Data Capture

Operational Visibility

Decentralized Trial Support

Capture, validate, and manage clinical trial data through connected workflows designed for decentralized, hybrid, and site-based studies.

Connected EDC + IWRS Workflows Across Clinical Trial Execution

Jeeva EDC helps research teams capture, validate, and manage clinical trial data through one connected operational platform. The platform supports real-time collaboration, standardized clinical data workflows, centralized audit trails, and operational visibility while reducing manual effort across study execution.

Jeeva supports compliant clinical trial execution aligned with GCP, FDA, EMA, and ICH guidelines.

Clients Love Jeeva Solutions

Compliance Programs Supported 

Features

Jeeva InterConnected Platform Simplifies End-to-End Trial Workflows

01

Standardized Clinical Data Capture

Apply standardized validation logic and workflows to improve data consistency and reduce manual reconciliation.

02

Real-Time Data Access & Visibility

Enable research teams to access clinical data, workflows, and operational insights in real time.

03

Improved Operational Efficiency

Reduce repetitive data management tasks through connected and centralized workflows.

04

Lower Operational Costs

Reduce operational burden and improve efficiency across clinical trial workflows.

05

Secure & Compliant Data Management

Support secure and compliant clinical trial operations aligned with regulatory requirements.

06

Audit Trails & Tracking

Maintain centralized audit trails and traceable workflow activity across study execution.

Electronic Data Capture Integrated with Randomization and Clinical Trial Management System

Configure electronic case report forms (eCRFs) in under two weeks

Implement protocol amendments in minutes or hours at no extra cost

A library of standardized eCRFs and study templates accelerates timelines

Monitor data quality and risks in real-time

Automate forms and procedures with centralized scheduling of visits

Adverse Events and Concomitant Medications (ConMeds)

Capture adverse events or symptoms with MedDRA data coding or controlled vocabularies.

Capture ConMeds reported by patients or site staff using the standardized terms from WHODrugDB.

Controlled vocabulary helps avoid spelling, typos, manual errors, or incomplete names.

Benefits

Real-Time Collaboration Across Clinical Trial Operations

Improve clinical data consistency through standardized and centralized workflows

Reduce delays across study startup, activation, and operational management workflows

Reduce manual data management effort through connected and streamlined workflows

Support standardized and validated clinical data capture across study environments

Support flexible randomization workflows through integrated EDC, IWRS, and unified CTMS

Testimonials

Client Testimonials

In looking for a software partner, our research coordinators and investigators in the field could call the Jeeva team anytime, get reliable support, and have reassurance as we enroll patients on the go. You can count on Jeeva when time is of the essence in operationalizing a clinical trial.

Dr. Emmanuel Gorospe

Chief Medical Officer of KCRS

There is an urgent need for validated tools to help ensure the continuity and integrity of clinical trial operations during and beyond the pandemic.

Frank Sasinowski, JD, MPH

A Legendary Leader in Rare Diseases and Orphan Drugs Regulation

We are pleased to collaborate with Jeeva for the eCOA module for our investigator initiated observational study to understand toileting use by individuals with certain brain disorders

Dr. Terry Jo Bichell

CombinedBrain

We need to bring healthcare and product development costs down, especially in the developing world. Clinical trial costs are a significant part of product development costs. We are confident that by partnering with Jeeva, we can find the correct value-for-money proposition without compromising quality.

Shirish Arya

Director of Strategy at ImmunoACT

We are pleased to provide financial support - both in the form of a grant and an equity investment - to Jeeva. Jeeva is an excellent example of the kind of startup we look to support and pursuing an enormous market opportunity. We wish Dr. Rajasimha and his team the best of luck as they continue to build this company.

Sean Mallon

Vice President, Virginia Innovation Partnership Corporation (VIPC)

Jeeva is a best-in-class solution for gathering clinical information with best-in-class customer service—two thumbs up.

David Hirsch

Founder, Special Father's Network, 21st Century Dads Foundation

We are proud that Jeeva emerged as #1 on the National Science Foundation (NSF) Innovation-Corps Program leaderboard.

Josh Green, PMP

Director ICAP, Small Business Development Center, George Mason University

Jeeva is a leader in the clinical trials software industry, with faster patient recruitment, focusing on global patient engagement.

Christiaan Engstrom

Founder, Bullpen Club

Jeeva's easy-to-use software interfaces and detailed user manual are backed by outstanding support team! Jeeva's technology platform enables us to serve patients globally in their native language.

Nisha Venugopal, Ph.D

Associate Director, Patient Focused Research Programs, Indo US Organization for Rare Diseases

Jeeva is a game-changer for our rare diseases site/CRO. It is unfair to expect patients or healthy volunteers to visit a hospital or clinic when it is not necessary when a task can be effectively completed safely, remotely, and from the comfort of where they live.