Who We Serve

Clinical Solution for Research Investigators

Maximize the probability of your clinical trial success by accelerating patient enrollment and flexible operations

Whether it is investigator-initiated study, observational study, phase 0, 1, 2, 3, or 4 post-market trials, real-world evidence generation to supplement your randomized controlled clinical trial, maximizing the speed of patient enrollment is the proven way to minimize your risk.

Maximize the probability of your clinical trial success by accelerating patient enrollment and flexible operations
Jeeva interviewed hundreds of stakeholders of clinical trials

We interviewed hundreds of stakeholders of clinical trials

They expressed dissatisfaction and complained about the poor experience with clinical trials.

“Every clinical trial feels like the first-ever trial undertaken by mankind” “Delays in patient recruitment put the entire clinical trial at risk” “If there is one thing I could fix, I would maximize the speed of clinical trial”

Compliance Programs Supported  
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Good Clinical Practice Logo
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EU General Data Protection Regulation Logo
AICPA SOC 2 Certified
AICPA SOC 2 Certified
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9001 ISO Certified Image
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AWS Partner Network Reviwed Image
Reduces the logistical burdens on sites and participants by 70 %

With bi-directional communications, scheduling, eligibility screening, and remote touch-less electronic informed consent, investigators can rapidly enroll participants in clinical studies with participants safely reviewing the study material at their own convenience remotely from their own mobile device.

Combine a la carte tools into a single modular unified platform

We understand technology is a means to an end. We strive to achieve the right balance between the use of technology and expert human intervention to optimize trial operations. Clinical study teams spend hundreds of hours coordinating participants' schedules to ensure quality and compliance.

Accelerate patient recruitment timelines by 3x

Jeeva SaaS streamlines the workflows for eligibility screening, bi-directional communications, and remote electronic informed consents with a focus on accelerating timelines while improving the user experience. We focus on optimizing the study operations so you can focus on research outcomes.

Features for Patient Groups

Pre-screening
eConsent
Patient reported outcomes
Cost-effective
Outcome Assessments
Adverse Events

Testimonials

Client Testimonials

FAQ

We Hear You Loud and Clear! Clearing Up Your Jeeva Concerns

Ask our chat Agent in the bottom right-hand corner anything about us or our solutions.

What are the key reasons sponsors select Jeeva Clinical Trials for their studies?
How does Jeeva Clinical Trials collaborate with our chosen CRO partner?
Is Jeeva equipped to support complex, multi-country, or global clinical trials?
What level of real-time oversight and visibility do sponsors have within Jeeva?
How does Jeeva ensure compliance with validation, audit, and regulatory requirements?
Can Jeeva facilitate a smooth migration from our legacy clinical trial systems?
What are the key reasons sponsors select Jeeva Clinical Trials for their studies?

Sponsors choose Jeeva for our unified and modular eClinical platform, which accelerates trial timelines, enhances real-time oversight, and minimizes vendor management complexity. Whether for single or multi-country studies, Jeeva’s integrated solutions support efficiency and scale while reducing operational risks.

How does Jeeva Clinical Trials collaborate with our chosen CRO partner?

Jeeva seamlessly integrates with your CRO, supplying the technology platform and targeted services to complement the CRO’s operational expertise. Our approach preserves your preferred governance model and allows sponsors to retain control and oversight throughout the clinical trial lifecycle.

Is Jeeva equipped to support complex, multi-country, or global clinical trials?

Yes, Jeeva is designed for global operations. Our platform features multi-site management, built-in localization for language and regulatory requirements, and standards-based integrations that ensure smooth execution of complex, multi-country studies.

What level of real-time oversight and visibility do sponsors have within Jeeva?

Sponsors benefit from comprehensive, role-based dashboards that deliver real-time insights into enrollment rates, data quality metrics, risk indicators, and financial KPIs. This centralized visibility empowers proactive management and timely decision-making across all your studies.

How does Jeeva ensure compliance with validation, audit, and regulatory requirements?

Jeeva maintains rigorous Computer System Validation (CSV) processes, robust Standard Operating Procedures (SOPs), and consistently prepares inspection-ready documentation. These measures support both routine sponsor audits and regulatory inspections, ensuring ongoing compliance and peace of mind.

Can Jeeva facilitate a smooth migration from our legacy clinical trial systems?

Absolutely. Jeeva supports structured migrations with detailed data mapping, parallel system runs for verification, and thorough change management protocols. Our approach minimizes risk and downtime—enabling a seamless transition to modern, unified clinical trial management.