We Serve All Stakeholders of Clinical Research 

At Jeeva, 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: 

We Serve All Stakeholders - Who We Serve

A Platform that Addresses ClinOps Stakeholder’s Concerns

Who We Serve

Jeeva empowers study teams to:

Jeeva ePowers Study

All while boosting engagement between researchers and patients by email, SMS, audio calling, and video calling with a single login for a study from any browser-enabled mobile device.

Rare Disease Registries - Who We Serve

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 - Who We Serve

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 - Who We Serve

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 - Who We Serve

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

Compliance & Quality Programs Supported  

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. 

Live Demonstration of Jeeva eClinical

Client Testimonials

Client Testimonials

Ready to Explore Jeeva eClinical Cloud for Your Study? 

Jeeva eClinical Cloud modules and packages are designed to be disease-agnostic, device-agnostic, flexible, and modular to support patient-preferred decentralized or hybrid trial operations. Schedule a 30-minute call today to determine the fit. We will help you identify technology or protocol complexity gaps to enable an informed decision.