Jeeva eClinical Cloud's answer

1. Jeeva is built based on insights derived from over 2000 stakeholder interviews. We have listened to patients, clinical operations leaders, biotech and pharma sponsors, clinical research organization (CRO) leaders, caregivers, and patients.
2. From what we heard, people say that, “every clinical trial feels like the first trial ever undertaken by mankind.”
3. That’s because each trial is different, even experienced clinical specialists run into the same issues trial after trial, year after year.
4. We reverse engineered clinical operations and designed an all-in-one solution with your day-to-day and long-term challenges in mind.
5. Jeeva’s agile platform for decentralized and remote clinical trials offers all the advantages of cloud computing: remote access, on-demand capacity, increased system reliability, scalability, and lower costs.

Jeeva eClinical Cloud's answer

After suffering the loss of a child to a rare congenital disorder and a brother to a chronic disease, Jeeva founder and CEO Dr. Harsha Rajasimha decided to apply his years of postdoctoral training at the National Institutes of Health and the U.S. Food and Drug Administration, as well as his work in the healthcare and life science industry, to accelerating access to treatments for rare & chronic diseases by eliminating bottlenecks in the clinical trials process.

Jeeva identified travel requirements for clinical trial patients as a major barrier for sponsors to achieve timely patient recruitment and retention. The location of the investigator sites and the frequency of travel are barriers for patients to access life-saving treatment options. In addition, the COVID-19 pandemic is accelerating the demand to decentralize the way clinical trials are conducted. Sponsors, investigators, regulators, and participants all embrace the potential of digital technologies to reduce cost, increase speed, and ease the burden on participants in these studies.

Jeeva eClinical Cloud's answer

We provide great features designed to save you time and resources: 1. Rapid study implementation – Ability to recruit the first patient on day 1 2. Therapeutic area-agnostic hybrid and decentralized trials 3. Tremendously flexibile, accessible, and easy to navigate 4. Simplified study management 5. Language support 6. Fast data entry 7. Real time data access and ability to extract data for reporting 8. Flexible trial data export to spreadsheets, text files, etc. 9. Storage and retrieval of SOPs 10. Access information easily and securely