Full cycle product for Research and Development teams in Pharmaceutical Industry. The product includes Electronic Trial Master File, Trial Management, Logistics and Inventory, Electronic Document Management with eSignature support. That is suitable for regulated areas as it is fully compliant with 21CFR Part 11 requirements.
It is a modular eClinical SaaS platform that works for decentralized, hybrid, or traditional trials using a centralized schedule of visits and module configuration. The modules include eConsent, ePRO/eCOA/EDC, TeleVisits/VideoVisits, Adverse event capture with MedDRA coding, and patient engagement portal with SMS/email/audio/video communications/reminders/notifications.
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Jeeva eClinical Cloud's answer:
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
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