Human-Centric Software Solutions for Clinical Trial Management, Data Management, and Patient-Engagement in One Subscription

Protocol Design and Writing

Jeeva provides personalized assistance and expert guidance for protocol design and writing to ensure top-quality protocols that meet your needs.

Site Qualification, Monitoring

Ensure compliance with the protocol, Good Clinical Practice, Federal and local regulations, and institutional policies.

Patient Screening/Recruitment

Assessing individuals for eligibility, conducting physical exams and lab tests, and obtaining informed consent before enrolling participants in the clinical trial.


Automated process of assigning participants to treatment and control groups, assuming that each participant has an equal chance of being assigned to any group.

Data Management

Improves data quality by collecting, cleaning, and managing subject data in compliance with regulatory standards.


Complete clinical trial management system to manage and track clinical research activities within an institution.

Patient Engagement Portal

Automated communication portal to send communication and trial updates to research patients.


Ensure the integrity and quality of clinical trial data, enabling researchers to draw valid conclusions and make evidence-based decisions.

Report and Publication

Customized research reporting to analyze the study findings and details for sharing and enhancing patient care.

Unified Software Platform for Human-Centric Modern Clinical Trials Management in One-Login With Patient Engagement in 100+ Languages

What Can You Do with Jeeva One Login? 

Advantages of Jeeva One Login Clinical Trial Solution

Streamlined Workflow

Eliminate the need for multiple logins and disparate systems, reducing administrative burden and improving workflow efficiency.

Improved Data Integrity

Centralize data management and monitoring processes to ensure data integrity, accuracy, and compliance with regulatory standards.

Enhanced Collaboration

Foster collaboration and communication among study stakeholders, promoting transparency, accountability, and teamwork.

Increased Participant Engagement

Provide participants with easy access to study information and tools, enhancing engagement, retention, and overall study success.

Cost Savings

Reduce costs associated with manual data entry, duplicate data entry, and system integration by consolidating all trial management activities into a single platform.

eClinical Platform Highlights - Jeeva eClinical Cloud

Simplify Your Clinical Trial Operations Management With Unified Software

Make your next clinical trial far more efficient with Jeeva’s modern clinical trial management solution, all in one login. Whether it is protocol design, site selection and monitoring, patient recruitment and retention, clinical data management, biostatistics, and reporting or publications, Jeeva has fully integrated all these functions in an all-in-one software platform.

By automating manual, repetitive tasks, Jeeva minimizes errors and maximizes the efficiency of clinical studies with a single login. By decentralizing low-risk activities and centralizing high-risk activities in one secure database, Jeeva delivers a more secure platform solution for all your clinical trial management needs with the flexibility and control you need.

By integrating all these functions, Jeeva can utilize the power of AI better to help optimize your next clinical trial further.

Compliance Programs Supported 

Client Testimonials

Client Testimonials

Still Curious If Jeeva eClinical Software is a Good Fit for Your Study?

Jeeva’s Human-Centric Software Solution is designed to manage multiple clinical studies from one login. It helps streamline modern clinical trials workflows and eliminate nagging industry problems. Schedule a 30-minute call today to determine the fit. We will help you design and assess feasibility of complex protocols to enable an informed decision.