Jeeva’s patent pending eClinical cloud solution for rapid remote touch-less patient enrollment, electronic informed consent, and data collection to setup registries or natural history studies with bi-directional communication and frictionless user experience for coordinators and patients.
They all expressed dissatisfaction and complained about the poor experience with patient registries, lack of flexibility, or having made wrong choices early on in signing up with free registries but giving up control over their data.
Whether you are setting up a registry or natural history study, a flexible user-friendly platform that enables long-term engagement and puts you on a solid foundation is critical.
Jeeva eClinical cloud can save you time, money, and most importantly, help ensure patient groups can drive collaborations among all stakeholders around the valuable data collected to accelerate therapies.
With a software that is designed in a human-centric approach by a visionary patient advocate, bi-directional communications between patients and central coordinators, scheduling, eligibility screening, and remote touch-less electronic informed consent, patient foundations can rapidly enroll patients into registry studies remotely from the convenience of their own homes & mobile devices. Jeeva eClinical cloud achieves this by combining email campaigns, drop and drop form builder, electronic consent with signatures, and workflow configurations for rapid omnichannel patient recruitment.
Commercial software platforms designed for high-quality clinical data collection were meant solely for biopharmaceutical companies or CROs for use in clinical trials. These remain unaffordable to most non-profit patient foundations or academic groups. The freely available academic registry platforms are not of high enough quality or do not offer the necessary technical support necessary to empower patient groups to use them. Those that do provide these features tend to cause concerns around data sharing, governance, or ownership.
Patient groups are solely motivated by accelerating the otherwise slow pace of progress in the therapy development process. This means the software should enable rapid patient education & enrollment about the registry studies, their data sharing policies, commitment expected, and other aspects of the study in multimedia formats. A drag and drop user-friendly interface can help patient groups develop standard operating procedures to develop high-quality registries advised by clinical researchers.
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.
Jeeva Clinical Trials Inc.
