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

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

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

Jeeva platform & service is aligned with our vision to making CAR-T cell therapies affordable in emerging markets.
Rahul Purwar
Founder at ImmunoACT

Jeeva gave us exactly the configurations we needed for our Pivotal clinical trials. I appreciate the functionality of the system.
Mihaela Plesa, BA, CCRP
Director, Clinical Research Programs at Frantz Viral Therapeutics

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

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

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
