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.
Clinion EDC is the most Integrated Electronic Data Capture System in the Industry making your clinical trials faster and better. Our Electronic Data Capture Software accelerates the speed of your clinical trial by reducing deployment time, capturing data faster, timely study close-out and early data lock – all in a cost-effective manner providing the highest data quality, integrity and security. Clinion EDC integrates all the functionalities you need into one platform, from study setup to data management and reporting.
What can you expect? - Quick mid-study changes, no need to rely on tech support or take your study offline. - Accelerates data validation and processing by using form rules like edit checks and skip logic. - Support for complex, multi-center studies - Can be integrated with Clinion RTSM, Clinion ePRO and Clinion CTMS - Build studies in days with its easy to use interface and AI-enabled features. - AI-enabled Medical Coding Automation delivering highest data quality
Quick facts: • Over 90% of studies using Clinion EDC are deployed within 1-2 weeks (without the need for extensive training). • First EDC System to Integrate AI • Fastest growing EDC solution with a 150% growth rate in last 2 years
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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