Solutions
Clinical Research Protocol to Publication Solutions for IITs
Streamlined Support for Academic Principal Investigators: From Protocol Proposal Preparation to Publication.
Jeeva is proud to offer an affordable and comprehensive solution for academic principal investigators, supporting them from the initial protocol proposal preparation phase to publication.
Our end-to-end turnkey solution ensures a smooth and efficient workflow for Investigator Initiated Trials (IITs) or Investigator Sponsored Trials (ISTs), assisting academic researchers conducting interventional and observational studies.
Advantages for IITs or ISTs
01
Study Design and Protocol Writing Assistance
With our chief medical officer leading the way, Jeeva’s team assists you with study design and protocol writing. We offer expert guidance and support to ensure a robust and well-structured study.
04
Data Support and Analysis
Jeeva’s trials team, led by Dr. Harsha Rajasimha, provides the biostatistical and data informatics support necessary during planning and downstream data analysis.
02
Seamless eClinical Solution
Jeeva's eClinical solution, managed by a dedicated team, facilitates quick protocol and eCRF configuration, patient screening and enrollment, engagement, EDC, and monitoring, using a variety of communication channels.
05
Overcoming Funding Challenges
We understand the unique challenges of IITs and ISTs, including limited funding, academic sponsors, government grants, or charitable donations. Sometimes industry may grant the intervention at no cost to support the study.
03
Enhanced Study Configuration Solution
If the protocol utilizes remote patient informed consent, TeleVisits, eCOA, or other decentralized tools, our team easily “adds” these features to the study configuration under the same login.
06
Supporting Other Studies
Additional studies that can be categorized under this model are observational, patient-funded studies, academic medical center research, patient foundation studies, non-profit organizations conducting approved clinical research, patient registries, natural history studies, and other cohort studies aiming for scientific publication.
01
Study Design and Protocol Writing Assistance
With our chief medical officer leading the way, Jeeva’s team assists you with study design and protocol writing. We offer expert guidance and support to ensure a robust and well-structured study.
03
Enhanced Study Configuration Solution
If the protocol utilizes remote patient informed consent, TeleVisits, eCOA, or other decentralized tools, our team easily “adds” these features to the study configuration under the same login.
05
Overcoming Funding Challenges
We understand the unique challenges of IITs and ISTs, including limited funding, academic sponsors, government grants, or charitable donations. Sometimes industry may grant the intervention at no cost to support the study.
02
Seamless eClinical Solution
Jeeva's eClinical solution, managed by a dedicated team, facilitates quick protocol and eCRF configuration, patient screening and enrollment, engagement, EDC, and monitoring, using a variety of communication channels.
04
Data Support and Analysis
Jeeva’s trials team, led by Dr. Harsha Rajasimha, provides the biostatistical and data informatics support necessary during planning and downstream data analysis.
06
Supporting Other Studies
Additional studies that can be categorized under this model are observational, patient-funded studies, academic medical center research, patient foundation studies, non-profit organizations conducting approved clinical research, patient registries, natural history studies, and other cohort studies aiming for scientific publication.
01
Study Design and Protocol Writing Assistance
With our chief medical officer leading the way, Jeeva’s team assists you with study design and protocol writing. We offer expert guidance and support to ensure a robust and well-structured study.
02
Seamless eClinical Solution
Jeeva's eClinical solution, managed by a dedicated team, facilitates quick protocol and eCRF configuration, patient screening and enrollment, engagement, EDC, and monitoring, using a variety of communication channels.
03
Enhanced Study Configuration Solution
If the protocol utilizes remote patient informed consent, TeleVisits, eCOA, or other decentralized tools, our team easily “adds” these features to the study configuration under the same login.
04
Data Support and Analysis
Jeeva’s trials team, led by Dr. Harsha Rajasimha, provides the biostatistical and data informatics support necessary during planning and downstream data analysis.
05
Overcoming Funding Challenges
We understand the unique challenges of IITs and ISTs, including limited funding, academic sponsors, government grants, or charitable donations. Sometimes industry may grant the intervention at no cost to support the study.
06
Supporting Other Studies
Additional studies that can be categorized under this model are observational, patient-funded studies, academic medical center research, patient foundation studies, non-profit organizations conducting approved clinical research, patient registries, natural history studies, and other cohort studies aiming for scientific publication.
Features of Jeeva
Works on BYOD Approach (Bring Your Own Device)
Ease of Data Analysis
Customizable and Configurable
Accessible from Various Hardware Devices of Varying Screen Sizes.
Time Saving
Secure Data Storage
Video/Tele/SMS/Email Communications.
Offers Remote Patient Monitoring, Assessments, and Follow-Ups.
Real-Time Live Interactive Communication Options.
Compliance Programs Supported
Testimonials
Client Testimonials
In looking for a software partner, our research coordinators and investigators in the field could call the Jeeva team anytime, get reliable support, and have reassurance as we enroll patients on the go. You can count on Jeeva when time is of the essence in operationalizing a clinical trial.
Dr. Emmanuel Gorospe
Chief Medical Officer of KCRS
There is an urgent need for validated tools to help ensure the continuity and integrity of clinical trial operations during and beyond the pandemic.
Frank Sasinowski, JD, MPH
A Legendary Leader in Rare Diseases and Orphan Drugs Regulation
We are pleased to collaborate with Jeeva for the eCOA module for our investigator initiated observational study to understand toileting use by individuals with certain brain disorders
Dr. Terry Jo Bichell
CombinedBrain
We need to bring healthcare and product development costs down, especially in the developing world. Clinical trial costs are a significant part of product development costs. We are confident that by partnering with Jeeva, we can find the correct value-for-money proposition without compromising quality.
Shirish Arya
Director of Strategy at ImmunoACT
We are pleased to provide financial support - both in the form of a grant and an equity investment - to Jeeva. Jeeva is an excellent example of the kind of startup we look to support and pursuing an enormous market opportunity. We wish Dr. Rajasimha and his team the best of luck as they continue to build this company.
Sean Mallon
Vice President, Virginia Innovation Partnership Corporation (VIPC)
Jeeva is a best-in-class solution for gathering clinical information with best-in-class customer service—two thumbs up.
David Hirsch
Founder, Special Father's Network, 21st Century Dads Foundation
We are proud that Jeeva emerged as #1 on the National Science Foundation (NSF) Innovation-Corps Program leaderboard.
Josh Green, PMP
Director ICAP, Small Business Development Center, George Mason University
Jeeva is a leader in the clinical trials software industry, with faster patient recruitment, focusing on global patient engagement.
Christiaan Engstrom
Founder, Bullpen Club
Jeeva's easy-to-use software interfaces and detailed user manual are backed by outstanding support team! Jeeva's technology platform enables us to serve patients globally in their native language.
Nisha Venugopal, Ph.D
Associate Director, Patient Focused Research Programs, Indo US Organization for Rare Diseases
Jeeva is a game-changer for our rare diseases site/CRO. It is unfair to expect patients or healthy volunteers to visit a hospital or clinic when it is not necessary when a task can be effectively completed safely, remotely, and from the comfort of where they live.
Marshall Summar, MD, Ph.D
CEO, Uncommon Cures LLC
Jeeva is backed by excellent customer service. We are enjoying our seamless transition to this platform for our longitudinal cohort study. Flexibility in programming.
Dr. Lawrence Cheskin, MD
Professor and Chair, Nutrition and Food Studies, George Mason University
Jeeva platform & service is aligned with our vision to making CAR-T cell therapies affordable in emerging markets.
Rahul Purwar
Founder at ImmunoACT
Jeeva's simple and elegant video consenting solution saves me hundreds of hours of repetitive process of obtaining informed consent from study participants
Kimberly Chapman, MD, Ph.D.
Principal Investigator, Childrens National Medical Center
In looking for a software partner, our research coordinators and investigators in the field could call the Jeeva team anytime, get reliable support, and have reassurance as we enroll patients on the go. You can count on Jeeva when time is of the essence in operationalizing a clinical trial.
Dr. Emmanuel Gorospe
Chief Medical Officer of KCRS
There is an urgent need for validated tools to help ensure the continuity and integrity of clinical trial operations during and beyond the pandemic.
Frank Sasinowski, JD, MPH
A Legendary Leader in Rare Diseases and Orphan Drugs Regulation
We are pleased to collaborate with Jeeva for the eCOA module for our investigator initiated observational study to understand toileting use by individuals with certain brain disorders
Dr. Terry Jo Bichell
CombinedBrain
