Jeeva - Version eClinical Cloud - Scalable Modular SaaS Software for Clinical Trials
Jeeva's patent-pending modular solution is designed from the ground up on the most powerful cloud platform with one login from any browser-enabled mobile device for remote patient screening, education, enrollment, electronic informed consent, bi-directional communications via video calling, telemedicine, SMS, email, and evidence generation including electronic patient-reported outcomes and clinical outcomes assessments, with a modern user experience.
- Remote pre-screening patients for eligibility from multi-channels
- Remote patient enrollment with eConsent
- 4-channel communications: email, SMS, audio, and video
- Patient reported outcomes (ePRO or vPRO)
- Clinical Outcomes Assessments (eCOA or vCOA)
- Telemedicine or live video follow ups
We interviewed a couple thousand stakeholders of clinical research
Delays in patient recruitment & retention are keeping them up at night. Generating enough evidence of safety and efficacy of investigational new medicines is critical to get timely approval from regulatory agencies. Whether you are a patient group setting up a registry or natural history study, or a biopharma sponsor of a clinical trial, or a long-term follow-up study for gene therapy, Jeeva can save you time, and money while improving user experience for study team and trial participants.
Reduces the logistical burden on study teams and participants by 70%
With bi-directional communications, scheduling, eligibility screening, and remote touch-less electronic informed consent, investigators can educate and enroll participants safely from their own mobile devices. Investigator teams can avoid repetitive tasks and save 70% of their time during enrollment.
Packages that fit the budgets of academic researchers or quality needs of industry sponsored global clinical trials
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 optimize trial operations. Clinical study teams spend hundreds of hours coordinating participants' schedules to ensure quality and compliance.
Accelerates clinical research timelines by over 3X
Jeeva eClinical platform 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. We focus on optimizing the study operations so you can focus on patient outcomes.