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Centralize and Execute your Clinical Research Faster with AI Assistants!

Patient-Centric

Unified

AI-Assisted

Cost-Effective

Centralize patient recruitment, retention, and clinical data management, study completion

Streamline and automate manual tasks, activities, scheduling

Real-time collaboration between sponsors, CROs, sites, and patients

Maximize success with the metrics driven user-friendly clinical trial management software

Clinical Research Works Better When Everything Runs on One Unified Platform

Manage Connected Clinical Trial Workflows in One Place

Connect sponsors, CROs, sites, participants, workflows, and clinical data through one interconnected platform built for modern clinical trial execution.

Keep Patients Connected in 100+ Languages

Support connected communication between patients, coordinators, and research teams through multilingual engagement workflows.

Configure Workflows Around Your Study Requirements

Start with the workflows and platform modules you need and expand operational capabilities as your clinical trials evolve.

Solutions

Jeeva eClinical Cloud Streamlines the End-to-End Trial Workflows

Solutions

Everything You Need in One InterConnected Clinical Platform

Electronic Data Capture (EDC) + Randomization (IRT)

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

Electronic Data Capture (EDC) + Randomization (IRT)

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

eCOA / ePRO / eDiaries

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

eCOA / ePRO / eDiaries

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

Unified CTMS

Manage study operations, workflows, scheduling, and execution from one platform.

Unified CTMS

Manage study operations, workflows, scheduling, and execution from one platform.

Patient Engagement Portal

Support patients through connected communication, reminders, and engagement workflows.

Patient Engagement Portal

Support patients through connected communication, reminders, and engagement workflows.

TrialMagnet

Accelerate recruitment and participant engagement through connected enrollment workflows.

TrialMagnet

Accelerate recruitment and participant engagement through connected enrollment workflows.

Centralized Study Scheduler

Coordinate and automate patient visit scheduling across clinical workflows.

Centralized Study Scheduler

Coordinate and automate patient visit scheduling across clinical workflows.

eConsent

Enable remote, compliant, and patient-friendly digital consent workflows.

eConsent

Enable remote, compliant, and patient-friendly digital consent workflows.

eVisits

Support remote participation through integrated virtual trial experiences.

eVisits

Support remote participation through integrated virtual trial experiences.

Benefits

Designed for Modern Clinical Trial Execution

Reduce manual errors and improve operational consistency through centralized workflows and automated validation logic

Support secure and compliant clinical trial operations through HIPAA- and SOC2-aligned infrastructure

Reduce inefficiencies caused by fragmented systems and disconnected operational workflows

Accelerate study startup and reduce delays across trial activation workflows

Support multilingual participant engagement across 100+ languages

Improve coordination across sponsors, CROs, sites, and participant workflows

Support connected trial participation across decentralized and hybrid environments

Configure workflows around evolving study requirements through flexible operational infrastructure

Access ongoing operational support across modern clinical trial operations

Discover A Pricing Plan That Fits Your Clinical Trial Management Needs

We understand that your clinical trial is unique. Our standardized infrastructure is built to scale.

Our flexible pricing options are designed to accommodate your project sizes and budgets. From small-scale studies to large-scale, multi-center trials, we have the flexible solution for you!

Get your queries answered during our demo session together!

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Clients Love Jeeva Solutions

Compliance Programs Supported 

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.

We already have a system in place. How will your CTMS integrate with our existing systems?

Jeeva Clinical Trials is designed to seamlessly integrate with other systems and platforms, such as electronic health records (EHR), laboratory information management systems (LIMS), and third-party data sources. Our team can assist with integrations to ensure smooth data exchange and interoperability.

Can you demonstrate how Jeeva can improve efficiency and reduce errors compared to our current solution?

Yes, we are happy to schedule a demo. Please book a demo on this page.

How long is the typical implementation timeline? Will it be too complex and time-consuming?

Our team configures most clinical trial protocols in two to four weeks. We can work with you based on your study schedule and timelines.

What kind of support do you offer during the implementation process?

Jeeva Clinical Trials offers comprehensive support services, including implementation assistance, training programs, ongoing technical support, and dedicated account management. Our team is committed to ensuring the success of our clients with our platform.

Can you explain your pricing model? Is the software cost too high?

Jeeva’s implementation can be completed within weeks, depending on your chosen modules or full platform subscription. We provide comprehensive onboarding and training for your team, including hands-on workshops, user manuals, and ongoing support to ensure a smooth transition and rapid adoption.

How does the Jeeva software platform's return on investment (ROI) compare to the costs of our current software and CRO service provider(s)?

Depending on the modular vs. full CRO platform subscription, the ROI can be measured both in tangible and intangible terms. In tangible terms, Jeeva’s centralized cloud-hosted solution could deliver 30% to 70% direct cost savings. An average of 30% time saved in clinical trial execution. Indirect cost savings of personnel time, avoided lost revenues due to minimal configuration, amendments, and support delays. In intangible terms, The benefit of maximizing the study’s chances of success. Improved user and patient experience enabling you to walk the talk of patient-centricity. In the long term, the savings can be more significant for enterprises with multiple studies.

Our data is sensitive. Can you guarantee security?

Jeeva Clinical Trials follows industry best practices for data security and compliance, including encryption, access controls, audit trails, and regular security assessments.

What security measures do you have in place to protect our data?

Our platform is designed to meet regulatory requirements such as HIPAA, GDPR, and 21 CFR Part 11.

Are you compliant with industry regulations like HIPAA and GDPR?

Yes. Refer to our privacy policies and terms of service in the footer.

We already have a system in place. How will your CTMS integrate with our existing systems?

Can you demonstrate how Jeeva can improve efficiency and reduce errors compared to our current solution?

Yes, we are happy to schedule a demo. Please book a demo on this page.

How long is the typical implementation timeline? Will it be too complex and time-consuming?

Our team configures most clinical trial protocols in two to four weeks. We can work with you based on your study schedule and timelines.

What kind of support do you offer during the implementation process?

Can you explain your pricing model? Is the software cost too high?

How does the Jeeva software platform's return on investment (ROI) compare to the costs of our current software and CRO service provider(s)?

Our data is sensitive. Can you guarantee security?

Jeeva Clinical Trials follows industry best practices for data security and compliance, including encryption, access controls, audit trails, and regular security assessments.

What security measures do you have in place to protect our data?

Our platform is designed to meet regulatory requirements such as HIPAA, GDPR, and 21 CFR Part 11.

Are you compliant with industry regulations like HIPAA and GDPR?

Yes. Refer to our privacy policies and terms of service in the footer.

Centralize and Execute your Clinical Research Faster with AI Assistants!

Patient-Centric

Unified

AI-Assisted

Cost-Effective

Clinical Research Works Better When Everything Runs on One Unified Platform

Manage Connected Clinical Trial Workflows in One Place

Keep Patients Connected in 100+ Languages

Configure Workflows Around Your Study Requirements

Jeeva eClinical Cloud Streamlines the End-to-End Trial Workflows

Everything You Need in One InterConnected Clinical Platform

Electronic Data Capture (EDC) + Randomization (IRT)

Electronic Data Capture (EDC) + Randomization (IRT)

eCOA / ePRO / eDiaries

eCOA / ePRO / eDiaries

Unified CTMS

Unified CTMS

Patient Engagement Portal

Patient Engagement Portal

TrialMagnet

TrialMagnet

Centralized Study Scheduler

Centralized Study Scheduler

eConsent

eConsent

eVisits

eVisits

Designed for Modern Clinical Trial Execution

Reduce manual errors and improve operational consistency through centralized workflows and automated validation logic

Support secure and compliant clinical trial operations through HIPAA- and SOC2-aligned infrastructure

Reduce inefficiencies caused by fragmented systems and disconnected operational workflows

Accelerate study startup and reduce delays across trial activation workflows

Support multilingual participant engagement across 100+ languages

Improve coordination across sponsors, CROs, sites, and participant workflows

Support connected trial participation across decentralized and hybrid environments

Configure workflows around evolving study requirements through flexible operational infrastructure

Access ongoing operational support across modern clinical trial operations

Discover A Pricing Plan That Fits Your Clinical Trial Management Needs

Clients Love Jeeva Solutions

Compliance Programs Supported

Client Testimonials

Dr. Emmanuel Gorospe

Marshall Summar, MD, Ph.D

Dr. Terry Jo Bichell

Rahul Purwar

Mihaela Plesa, BA, CCRP

Dr. Emmanuel Gorospe

Marshall Summar, MD, Ph.D

Dr. Terry Jo Bichell

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

We already have a system in place. How will your CTMS integrate with our existing systems?

Can you demonstrate how Jeeva can improve efficiency and reduce errors compared to our current solution?

How long is the typical implementation timeline? Will it be too complex and time-consuming?

What kind of support do you offer during the implementation process?

Can you explain your pricing model? Is the software cost too high?

How does the Jeeva software platform's return on investment (ROI) compare to the costs of our current software and CRO service provider(s)?

Our data is sensitive. Can you guarantee security?

What security measures do you have in place to protect our data?

Are you compliant with industry regulations like HIPAA and GDPR?

We already have a system in place. How will your CTMS integrate with our existing systems?

Can you demonstrate how Jeeva can improve efficiency and reduce errors compared to our current solution?

How long is the typical implementation timeline? Will it be too complex and time-consuming?

What kind of support do you offer during the implementation process?

Can you explain your pricing model? Is the software cost too high?

How does the Jeeva software platform's return on investment (ROI) compare to the costs of our current software and CRO service provider(s)?

Our data is sensitive. Can you guarantee security?

What security measures do you have in place to protect our data?

Are you compliant with industry regulations like HIPAA and GDPR?

Compliance Programs Supported 