Save 70% of your time and maximize the probability of success of your clinical study

Avoid common pitfalls by starting your cohort study, patient registry, observational data collection, or clinical trial on Jeeva eClinical cloud platform. Save over 70% of the effort involved in toggling between numerous tools, coordination between multiple channels of engagement between study team and participants, participants use their own mobile device, and study specific data governance.

We interviewed hundreds of stakeholders of clinical research

They all expressed dissatisfaction and complained about the poor experience with clinical trials.

Whether you are working with a patient group that is setting up a registry or natural history study, or with biotech that is sponsoring a long-term follow-up study for gene therapy, Jeeva Clinical can save you time and money while improving recruitment and retention of trial participants.


  • Pre-screening & eConsent
  • Video/Telemedicine/SMS/Email Communications
  • Patient reported outcomes
  • Lab Reports Integration
  • Clinical Outcomes Assessments
  • Adverse Events
Reduces the logistical burden on study teams and participants by >70 percent

With bi-directional communications by video/audio/SMS/emails, scheduling, eligibility screening, and remote touch-less electronic informed consent, investigators can rapidly engage and enroll participants in clinical studies remotely from where they are on their own mobile devices.

Packages that fit the budgets of research investigators or quality needs of global multi-site studies

We understand technology is a means to an end. We strive to achieve the right balance between the use of technology and expert human intervention to maximize flexibility in clinical operations. Study teams can save hundreds of hours in coordinating participants' schedules to ensure quality and compliance.

Reduces the timelines for study startup and participants recruitment by >3x

Jeeva SaaS streamlines the workflows for eligibility screening, bi-directional communications, and remote electronic informed consents with a focus on accelerating timelines while improving the user experience. The software maximizes flexible study operations so you can focus on patient outcomes.

Patient Registries and 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.

Long-Term Follow Up Studies

Cell and 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 places 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 trials management or electronic data capture tools were designed for traditional brick and mortar clinical trials that usually span less than three years.  Our purpose-designed solution for five, 10, or 15-year follow up studies is the perfect solution for these studies.

man with wheelchair in van
patient in wheelchair with nurse

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.