eClinical Solutions

Therapeutic Areas

About Us

Resources

SSCCHHEEDDUULLEE AA DDEEMMOO

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
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.
Marshall Summar, MD, Ph.D
CEO, Uncommon Cures LLC
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
Jeeva platform & service is aligned with our vision to making CAR-T cell therapies affordable in emerging markets.
Rahul Purwar
Founder at ImmunoACT
Jeeva gave us exactly the configurations we needed for our Pivotal clinical trials. I appreciate the functionality of the system.
Mihaela Plesa, BA, CCRP
Director, Clinical Research Programs Frantz Viral Therapeutics

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

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.

Marshall Summar, MD, Ph.D

CEO, Uncommon Cures LLC

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

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 CDM services do you offer?

Jeeva provides end-to-end Clinical Data Management (CDM) services, including robust data management plan development, CRF (Case Report Form) design tailored to your protocol, custom edit-check programming, and reconciliation of serious adverse events (SAE), pharmacokinetics (PK), and central laboratory data. Our team also supports clean data lock and database closure for regulatory submissions.

Do you manage clinical data standards (CDASH/SDTM/ADaM)?

Yes, Jeeva maintains comprehensive data standards governance and delivers outputs compliant with industry-recognized standards such as CDASH, SDTM, and ADaM. This ensures your clinical data sets are submission-ready, facilitates biostatistics analysis, and streamlines regulatory submissions.

How do you handle mid‑study EDC changes?

Jeeva employs a controlled change management process, including thorough impact analysis, rigorous validation, and release of versioned updates. This allows you to efficiently implement protocol amendments with full traceability and minimal disruption to ongoing studies.

What’s your approach to clinical research data cleaning and queries?

Jeeva uses a risk-based data review strategy, central monitoring signals, and automated KPI-driven query cycles to accelerate data cleaning and minimize cycle times. Our EDC system supports proactive identification and resolution of data discrepancies, ensuring high-quality, reliable datasets.

Can you take over live clinical studies?

Yes, Jeeva offers expertise in mid-study transitions and rescue studies. We utilize structured migration playbooks, detailed data mapping processes, and dual-running approaches to seamlessly transfer ongoing studies to our EDC platform, mitigating risk and ensuring data continuity throughout the transition.

How do you ensure clinical trials inspection readiness?

Jeeva maintains complete, traceable audit trails, robust study documentation, and alignment with the Trial Master File (TMF/eTMF) requirements. Our approach keeps your clinical trials inspection-ready at all times, supporting successful regulatory audits and submissions.