Simplify Patient-Reported Outcomes Collection Across Clinical Trials
Patient Engagement
Connected Workflows
Decentralized Trial Support
Collect patient-reported outcomes through multilingual and patient-friendly workflows designed for decentralized, hybrid, and site-based clinical trials.
Connected eCOA Workflows for Modern Clinical Trials
Support remote participation through secure assessments, multimedia questionnaires, and BYOD-enabled workflows across decentralized and hybrid studies.
Enable participants, caregivers, and observers to complete multilingual outcome assessments while improving operational visibility and reducing manual coordination across study execution.
Clients Love Jeeva Solutions
Compliance Programs Supported
Solutions
How our eCOA Platform Works
Accelerate Clinical Trials Through Connected eCOA Workflows
Real-Time Data: The Future of Informed Decision-Making
Driving Success with Seamless Participant Engagement
Minimizing Delays
Strengthening Patient Security
Maintaining Accuracy and Compliance
Real-Time Data: The Future of Informed Decision-Making
Researchers gather and examine patient-reported outcomes instantaneously, enabling quick modifications to the trial protocol in response to protocol amendments.
Accelerate Clinical Trials Through Connected eCOA Workflows
Real-Time Data: The Future of Informed Decision-Making
Researchers gather and examine patient-reported outcomes instantaneously, enabling quick modifications to the trial protocol in response to protocol amendments.
Driving Success with Seamless Participant Engagement
Minimizing Delays
Strengthening Patient Security
Maintaining Accuracy and Compliance
Accelerate Clinical Trials Through Connected eCOA Workflows
Real-Time Data: The Future of Informed Decision-Making
Researchers gather and examine patient-reported outcomes instantaneously, enabling quick modifications to the trial protocol in response to protocol amendments.
Driving Success with Seamless Participant Engagement
Minimizing Delays
Strengthening Patient Security
Maintaining Accuracy and Compliance
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.
Is it BYOD for patients to use eCOA and ePRO Software?
Yes. Jeeva’s eCOA/ePRO platform fully supports “Bring Your Own Device” (BYOD) deployment, allowing participants to use their own smartphones or tablets for reporting outcomes. We also offer provisioned devices for participants who need them, ensuring maximum accessibility and flexibility across diverse patient populations.
Do you support validated eCOA instruments and licensing?
Absolutely. Jeeva seamlessly integrates licensed and validated Clinical Outcome Assessments (COAs), manages all necessary permissions, and ensures each instrument version is properly controlled. This facilitates compliance and reliability in both global and local studies.
What if a patient is offline? Does your eCOA software support offline data capture?
Our platform supports offline data capture, so patients can complete assessments even without internet access. Responses are securely stored on the device and automatically synced with the study database once the device reconnects, minimizing data loss risk and maintaining study continuity.
How does your eCOA/ePRO software handle patient reminders?
Jeeva employs adaptive reminders, delivered via SMS, email, and in-app notifications, that are intelligently timed to patients’ visit windows and local time zones. This personalized approach reduces the likelihood of missed entries and improves data completeness.
Are diaries and clinician‑reported outcomes supported?
Yes. Jeeva’s software supports comprehensive electronic diaries, clinician-reported outcomes (ClinRO), and caregiver workflows. Each role is enabled with tailored, role-based access to streamline workflow, ensure data privacy, and enhance study flexibility.
Can we monitor compliance in real time?
Yes. Jeeva’s real-time compliance dashboards give study teams instant visibility into data completion rates, timeliness of responses, and identification of outlier data, enabling proactive follow-up and rapid intervention when needed.
Is it BYOD for patients to use eCOA and ePRO Software?
Yes. Jeeva’s eCOA/ePRO platform fully supports “Bring Your Own Device” (BYOD) deployment, allowing participants to use their own smartphones or tablets for reporting outcomes. We also offer provisioned devices for participants who need them, ensuring maximum accessibility and flexibility across diverse patient populations.
Do you support validated eCOA instruments and licensing?
Absolutely. Jeeva seamlessly integrates licensed and validated Clinical Outcome Assessments (COAs), manages all necessary permissions, and ensures each instrument version is properly controlled. This facilitates compliance and reliability in both global and local studies.
What if a patient is offline? Does your eCOA software support offline data capture?
Our platform supports offline data capture, so patients can complete assessments even without internet access. Responses are securely stored on the device and automatically synced with the study database once the device reconnects, minimizing data loss risk and maintaining study continuity.
How does your eCOA/ePRO software handle patient reminders?
Jeeva employs adaptive reminders, delivered via SMS, email, and in-app notifications, that are intelligently timed to patients’ visit windows and local time zones. This personalized approach reduces the likelihood of missed entries and improves data completeness.
Are diaries and clinician‑reported outcomes supported?
Yes. Jeeva’s software supports comprehensive electronic diaries, clinician-reported outcomes (ClinRO), and caregiver workflows. Each role is enabled with tailored, role-based access to streamline workflow, ensure data privacy, and enhance study flexibility.
Can we monitor compliance in real time?
Yes. Jeeva’s real-time compliance dashboards give study teams instant visibility into data completion rates, timeliness of responses, and identification of outlier data, enabling proactive follow-up and rapid intervention when needed.