Maximize research productivity with Jeeva's compliant remote electronic informed consent (eIC)
Clinical investigators, researchers, and coordinators are well aware of the logistical burdens of the in-person informed consent at clinics. The repetitive nature of explaining the study process, risks, benefits, sample or data use, paperwork, and answering frequently asked questions drain research productivity. We heard you. We designed a compliant solution that maximize productivity with minimized burden on patients and researchers.
We interviewed hundreds of researchers, coordinators, and patients
They all agreed proper informed consent is an important part of building trust between researchers and patients. They also complained about the burden of informed consent, lack of flexibility for in-person or remote electronic informed consent, or repetitive nature of the process. Many studies are terminated even before starting due to the number of investigator hours or patient travel burden required for in-person informed consent. Jeeva eClinical cloud saves you time, burden, and maximizes research productivity!
Reduces the logistical burden and time for clinical researchers by over 90 percent
Clinical investigators spend at least 30 minutes per patient for proper in-person informed consent. For a 1000 patient study, that's 500 hours of a MD/PhD physician investigator's time. Just not practical for many research studies and unnecessary in many scenarios, particularly when a new investigational drug is not involved. Jeeva remote electronic informed consent (eIC) solution empowers clinical researchers and coordinators with a compliant way of ensuring the same goal remotely without the associated repetitive tasks or burden.
The software subscription model that fits the budgets of academia and industry without compromising the required information exchange
Jeeva's cloud-based software as a service (SaaS) means flexibility to access the software as needed and pay per month or year and based on the number of patients in your study. We have packages that fit most budgets. Contact us to discuss your use case, study duration, and size. Our product team will work with you closely to quickly identify the right configuration and set you up. SaaS also means zero installation and works on all browser-enabled mobile devices.
Enables rapid patient enrollment from numerous channels
The software should enable rapid patient education of patients before the eligibility screening, during enrollment, and throughout the study. Some studies have a pre-identified list of patients while others will benefit from the ability to find, screen, and enroll patients from a variety of channels such as social media channels such as Facebook groups, email campaigns, WhatsApp, or web portals. Dynamic multi-media content management and drag and drop user-friendly interface for building enrollment workflow empower clinical researchers to execute informed consents remotely with minimal human resources.