We listened to a couple thousand stakeholders of clinical research

Delays in patient recruitment and retention, ensuring diversity, equity, and inclusion, generating quality clinical evidence of safety and efficacy of treatments, tracking patients adherence to medication, and compliance with regulatory agencies such as Institutional Review Boards, FDA, EMA, GDPR, and other guidelines are critical factors.

Accelerate Patient Recruitment & Retention

85% of clinical trials are delayed due to the slow pace patient enrollment. 30% of clinical trials fail because they cannot meet their target enrollment. Every day delayed causes biopharmaceutical sponsors a loss of $600K to $8M. Patient recruitment involves identification of patients matching the inclusion & exclusion criteria for the specific clinical trial. Most patients screened do not match. Then, enrolling those small number of matching patients into the study. Only about 3% of matching patients are choosing to enroll in clinical trials. 1 out of 4 patients not enrolling cite logistical burden as the primary reason.

Maximize Diversity, Equity, and Inclusion

The randomized controlled clinical trials have been historically successful in enrolling Caucasian adult male participants from affluent backgrounds. Less than 10% of clinical trials include children. Women and minorities are less likely to participate in clinical trials as they have more logistical burdens and special needs such as childcare, transportation, and loss of pay. 

Generate Reliable Clinical Evidence

Clinical research involves generation of high quality reliable clinical evidence of patient safety and outcomes. The traditional model of generating evidence during patients’ in-person visits to brick-and-mortar sites can no longer be solely relied on. Researchers and patients are questioning traditional models and seeking increased flexibility in the post-pandemic world.   

Maximize Patient Adherence to Medication

Sponsors and regulators rely on the evidence generated by study volunteers’ use of Investigational new therapies as prescribed by their investigators in the approved clinical trial protocols. If patients miss medication routine or deviate from the protocol, that may deny the therapy its fair chance of demonstrating efficacy. Hence, ensuring that study participants adhere to clinical protocol is a critical factor.

Minimize Regulatory Risk and Maximize Compliance

Clinical trials are highly regulated at various levels including by institutional review boards (IRBs), human subjects protection guidelines, Good clinical practice (GCP) guidance by international code of harmonization (ICH) E6 R2, data protection guidelines guidelines such as GDPR, and other local or regional guidelines. The burden of ensuring regulatory compliance of technology solutions deployed in a clinical trial rests with the sponsors. Hence, adoption of newer innovative technologies introduces risks for sponsors. 

Walk the Talk of Patient-Centricity

Patients are the center of clinical research. They are critical partners and not “subjects”. Yet, many clinical trials fail to incorporate patient voices early during clinical trial protocol development or logistical planning. Educating and informing patients about the goals of the trial and gathering their inputs are critical success factors.  

Modular Software as a Service (SaaS) Subscription 

Helps clinical researchers manage study budget on a simple per study participant subscription basis.

Automated Enrollment Workflow

Remote eConsent

Patient-Reported Outcomes (ePRO/vPRO)

Clinical Outcomes Assessments (eCOA/vCOA)

Video, Audio, SMS, & Email Communications

Telemedicine or Video-calling

Upload Lab Reports

Adverse Event Reporting

Testimonials

4th

Still curious if Jeeva eClinical Cloud is a good fit for your study?

Jeeva is designed to be disease-agnostic, device-agnostic, flexible, and modular to support patient preferred hybrid trial operations. Schedule a 30 minute call today to efficiently determine the fit. We will help you make an informed decision.

November 15, 2021
    

Jeeva software is much needed to reduce the logistical burden on patients and families who depend on clinical trials for life saving treatments.

November 15, 2021
    

There is an urgent need for validated tools to help ensure continuity and integrity of clinical trial operations during and beyond the pandemic.

November 15, 2021
    

Jeeva is a best in class solution for gathering clinical information.

November 15, 2021
    

Jeeva represents the next generation of software platforms for flexible clinical research including for pediatrics.

November 15, 2021
    

Jeeva's remote electronic informed consent module is of immediate need for numerous projects at our rare disease institute.

November 15, 2021
    

#NoGoingBack to preserve the progress in clinical trials

November 15, 2021

Jeeva will enhance the clinical trial experience for both the participants and research teams, improve clinical trial performance and success, reduce trial costs and reduce the travel burden on participants who will be enrolled in long term safety follow up studies for cell and gene therapy trials for up to 15 years.

November 15, 2021

We are proud that Jeeva went on to emerge #1 on the leaderboard of the National Science Foundation (NSF) Innovation-Corps Program.

November 15, 2021

Having graduated with MD degree from Vanderbilt University 20 years ago and user of RedCap, I find Jeeva refreshingly easy to use. It's going to be a game changer.

November 15, 2021

Jeeva is about making Clinical Trials simpler, more reachable and at the end help us make our world a better place by getting people access to medicines sooner.

November 15, 2021

We evaluated other competing products and they are either too expensive to fit within the budgets of academic investigator-initiated studies, or they have partial only coverage of needed features, thus requiring my staff to juggle between multiple tools, causing process breakdowns.

November 15, 2021

Jeeva will allow for the easy collection of additional data, which in turn may lead to more robust measures of both safety and efficacy.

November 15, 2021

The Indo US Organization for Rare Diseases has been working with Jeeva's versatile platform to standup a patient concierge services.

November 15, 2021

Jeeva is a leader in the clinical trials recruitment industry with a focus on global patient engagement.

November 15, 2021

The Jeeva eClinical Cloud offers a novel way forward.

November 15, 2021

Jeeva is solving an important problem (travel burden, optimization of clinical research operations) specific to rare disease communities with your innovative hybrid decentralized clinical trials SaaS technology platform.

November 15, 2021

Jeeva is solving important problems that are unique to rare diseases communities with their innovative hybrid decentralized clinical trials SaaS technology platform.

November 15, 2021

Platforms like Jeeva are much needed to help ensure continuity and integrity of trials even during a pandemic.

November 15, 2021

I had already reviewed and rejected other traditional clinical trial proposals and was pleasantly gratified to see the Jeeva platform essentially addressed/solved all my major concerns.

November 15, 2021

They also have best in class customer service. Two thumbs up.

November 15, 2021

We are switching our 5-year longitudinal study to Jeeva's single login from 3 different tools.

November 15, 2021

It is my opinion that the execution of a decentralized clinical trial as proposed and implemented by Jeeva Informatics would be a very attractive and costeffective solution for us.

November 15, 2021

Very happy with the easy-to-use  interface and the detailed user manual which are supported by a highly responsive
team!

November 15, 2021

Our research team believes that Jeeva's unique vision to make clinical research simple by incorporating research into the lifestyle of consumers via mobile apps that run on their own devices, is the way forward.

November 15, 2021

We expect that adopting the Jeeva platform will reduce the time demand on our research team for recruitment and
meeting coordination by at least 25%, enabling us to focus on the participants and the data.

November 15, 2021

Jeeva can deliver dramatic cost and efficiency improvements in recruitment, retention and management of research
trial participation, free of geographic and demographic limitations.

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