Finding and keeping participants in oncology trials is challenging due to the complexity and intensity of treatments. Jeeva’s platform enhances recruitment by reaching a wider patient pool and boosting retention with tailored support and communication tools that keep participants engaged and informed.
Oncology trials often involve large, complex datasets. Jeeva simplifies this with centralized data management, allowing researchers to efficiently organize, access, and analyze clinical data, reducing the risk of errors and improving decision-making.
Oncology protocols are stringent, and deviations can lead to unreliable data. Jeeva’s software provides automated reminders and an easy-to-use interface to ensure participants and sites adhere strictly to study protocols.
Timely data analysis is crucial for effective oncology treatments. Jeeva facilitates real-time monitoring and reporting, offering up-to-date insights into patient responses and trial progress for quicker, informed decision-making.
Maintaining high safety standards and ensuring regulatory compliance can be daunting. Jeeva provides built-in compliance features and rigorous data security measures, ensuring adherence to regulatory requirements and prioritizing patient safety.
Coordinating between multiple research sites and teams can be cumbersome. Jeeva streamlines communication and data sharing, ensuring all stakeholders have access to the same information, which promotes collaboration and unity throughout the trial.
Jeeva offers real-time centralized dashboards that streamline the monitoring of oncology trials by providing researchers with instant access to critical data. This feature enables swift assessments and insights, ensuring you’re always informed and can respond promptly to evolving trial dynamics.
Jeeva's software simplifies managing the logistical complexities of oncology trials. It automates routine tasks, organizes schedules, and minimizes paperwork. This reduction in logistical stress allows research teams to focus more on patient care and study outcomes.
Expand your oncology research reach by conducting research in 100+ languages to facilitate virtual trials and remote participation. This enables you to effortlessly conduct multi-site research across various regions, providing access to a diverse pool of participants and data.
We provide premium 24/7 study support, ensuring that your research is continuously monitored and assistance is available whenever needed. Our round-the-clock support helps keep your trial running smoothly, addressing any issues promptly to maintain high study standards.
You may derive most value when your clinical operations infrastructure is not set up yet. However, even if some of your infrastructure is in place, Jeeva can complement what you have with modularity and automation.
There’s no upfront CapEx. Our pricing is usage-based, and partners see ROI by reducing site coordination and compliance overhead.
Jeeva is fully validated, GCP-aligned, 21 CFR Part 11 and GDPR compliant. We’re already used by academic medical centers and sponsors in regulated trials.
Jeeva provides centralized dashboards that display real-time data from all active sites, enabling researchers to monitor patient responses, track overall trial progress, and make informed decisions based on up-to-date information.
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.
Still Curious If Jeeva Human-Centric Clinical Research Software Is a Good Fit for Your Study?
Jeeva Clinical Trials Inc.