Who We Serve
We Serve All Clinical Trial Stakeholders
At Jeeva, we have solution for all clinical trial stakeholders including CROs, Sponsors, Researchers, and Patients. We are passionate about making clinical research faster, more accessible, diverse, and least burdensome for researchers and patients. Validated, high-quality, compliant software systems are needed for remote patient education, enrollment, evidence generation, and retention in a variety of research programs involving human subjects. These include:
Biopharmaceutical sponsors for their phase 0, 1, 2, 3, or 4 clinical trials
A white-labeled solution for Contract Research Organizations (CROs) as partners
Patient advocacy groups for their patient registry or natural history studies
Academic researchers for their investigator-initiated trials and longitudinal cohort studies
Public health research programs involving population-scale surveillance, safe quarantine, or safety studies
Solutions
A Platform that Addresses Clinical Trial Stakeholders' ClinOps Concerns
Jeeva empowers study teams to:
Remotely screen, recruit and retain more participants faster
Elevate electronic patient-reported outcomes (ePRO) to a whole new level during a live video call (vPRO).
Directly capture electronic study data, lab reports, safety, medical history, and clinical outcomes assessments (eCOA) using the drag-and-drop form builder including during a live video call between investigator and patient.
Minimize investigator burden by capturing patient self-reported information at a time and place convenient for the patient.
Maximize patient satisfaction, by providing flexibility for them to complete study participation and follow-up visits remotely or in person.
Reduce operational costs by minimizing the need for in-person monitoring visits as all study staff will have real-time access to the central clinical database.
Rare Disease Registries or Natural History Studies
Longitudinal cohort studies collect clinical, behavioral, lifestyle, and environmental data from participants in real-world settings over extended periods of time. Our bring-your-own-device platform makes it easy for study investigators to onboard, engage, and retain participants. The FDA and NIH's National Center for Advanced Translational Sciences have encouraged patient groups to drive establishment of high-quality institutional review board-approved patient registries and natural history studies.
Chronic Diseases Clinical Studies
Patients suffering from chronic conditions such as Diabetes, Cardiovascular, or neurobehavioral disorders lack the high motivation to take on the significant burden of participating in a clinical trial. By utilizing a protocol design that minimizes patient burden by enabling the flexibility of remote enrollment, participation, and long-term engagement, you can maximize the probability of trial success. With a single integrated and modular software subscription service that can be flexibly configured to support complex study designs, you can win more global clinical trial opportunities with sponsors.
Investigator Initiated Trials
Our experienced coordinators provide the highest quality of video conferencing visits for patients and caregivers. Our goal is to help simplify and manage the trial operations to minimize burden, reduce dropouts, improve compliance, and accelerate the development of therapies. Investigator initiated single site studies suffer from lack of funding necessary to conduct certain large-scale, real-world evidence, observational, or drug repurposing studies of medicines already proven safe. Jeeva eClinical cloud platform offers a cost-effective solution to quickly setup and conduct clinical studies of any scale or duration, with or without patient travel involved.
Long-Term Follow Up Studies
Gene therapy trials typically involve one-time therapy administration with long-term follow-up with patients for safety monitoring. Physical site visit requirements over a long period of time, place an undue burden on trial participants. Jeeva simplifies this process by fitting the trial into the lifestyle of patients. Cell and gene therapies are the most advanced form of one-and-done treatments for patients with rare genetic diseases including cancer. FDA guidelines in January 2020 require sponsors of such therapy trials to monitor patients over extended periods of time to better understand the durability of these treatments. Most of the existing clinical trial management or electronic data capture tools were designed for traditional brick and Read More
Recognition and Membership
Get Live Demonstration of Jeeva eClinical Cloud on Your Study Protocol
We interviewed a couple of thousand stakeholders of medical research including patients, researchers, sponsors, CROs, regulators, and key opinion leaders. They all expressed dissatisfaction and complained about the poor experience with conducting or participating in clinical trials, lack of flexibility, or having made wrong choices early on in trial design resulting in protocol amendments or patient reconsenting, logistical burdens of patient recruitment, and retention. Our collective response is the Jeeva eClinical Cloud software as a service (SaaS) platform that addresses all stakeholder concerns and provides a flexible user experience on any browser-enabled mobile device. Accelerating timelines, minimizing cost, enabling collaborations among all stakeholders on a single platform, and bi-directional communications between study users and patients by email, SMS, audio, and video calling.
Testimonials
