Founded by a rare dad on a mission to make orphan drug clinical trials universally accessible, Jeeva’s software solutions are designed to empower rare disease research by engaging patients through the clinical trial journey.
Connecting patients with rare diseases to clinical trials can be daunting due to their scarcity. Jeeva simplifies this through global virtual recruitment tools, reaching patients from diverse locations to maximize participation in your trials.
Rare disease populations are often spread across wide areas. Jeeva facilitates participation through a remote patient engagement portal and omnichannel communications, reducing travel burdens, and enhancing inclusivity.
Rare diseases may have simple genetics (e.g., single-gene disorders) but complex phenotypes. Jeeva streamlines complex data collection with user-friendly interfaces for capturing genetics, laboratory test data, photos or videos, and much more.
Navigating diverse regulatory landscapes for rare diseases is challenging. Jeeva provides built-in compliance features and documentation tools that help ensure your trials seamlessly adhere to varying global regulatory standards.
Keeping patients engaged over the long duration typical of rare disease trials is difficult. Jeeva addresses this with personalized communication and support tools that keep participants informed and motivated throughout the study.
Bringing together specialized experts and resources is often a barrier in rare disease research. Jeeva facilitates collaboration through virtual platforms, enabling instant access to a network of experts and shared resources, fostering efficient study execution.
Jeeva’s platform is highly adaptable, allowing researchers to tailor the software to meet the specific needs of each rare disease trial. This customization supports the unique protocols and methodologies required for these specialized studies, ensuring a perfect fit for your research objectives.
Get your rare disease trial up and running swiftly with Jeeva's streamlined setup process. Our software minimizes the time spent on administrative tasks, enabling you to launch studies faster and focus on what truly matters—advancing treatment options for rare conditions.
Jeeva reduces the risk of data errors by automating data entry and management processes. This automation ensures accurate and reliable data capture, freeing your team from manual errors and allowing for more consistent and dependable study results.
Our platform supports on-the-go data collection, enabling participants to report information conveniently from their own devices, no matter where they are. This flexibility is crucial for reaching dispersed populations and capturing real-time data efficiently and accurately in rare disease research.
An enterprise access to all clinical trials under the organization in a single login.
Rapid configuration of a complex protocol and the ability to make mid-study amendments with little or no delays.
Jeeva Clinical Trials follows industry best practices for data security and compliance, including encryption, access controls, audit trails, and regular security assessments. Our platform is designed to meet regulatory requirements such as HIPAA, GDPR, and 21 CFR Part 11.
Founded by a rare dad on a mission to make orphan drug clinical trials universally accessible, Jeeva’s software solutions are designed to empower rare disease research by engaging patients through the clinical trial journey.
Jeeva Clinical Trials Inc.