Jeeva eClinical Cloud
Clinion CTMS
Clinion eCOA
Medidata CTMS
IQVIA
OpenClinica
Medrio ePRO
Medidata Rave
ClinicalHawk EDC
Viedoc
Clinion EDC
RTMS
Veeva Vault
Medidata CTMS
Castor EDC
SCADA
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.
An Electronic Data Capture software streamlines the gathering of trial patient data for early to late-stage clinical research phases, as well as post-approval studies. An adaptable and scalable EDC system is used by Pharma, Biopharma, Medical Device Companies, across the clinical research industry. ClinicalHawk EDC is a complete Cloud-Based programme with a Flexible structure that allows the users for Easy Data Collection from trial subjects. Users will be able to Quickly and Accurately Record Quality Data with Integrated Online Editing Check and Query Management options. The system’s Robust Reporting features aid Research Team Researchers to perform Real Time Data Analysis.
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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
Clinion CTMS - Integrated Solution To Plan, Manage and Track All Your Studies
Viedoc - EDC, ePRO, eCRF, eTMF, CDMS, electronic data capture, clinical trial and PMS software
Clinion eCOA - Clinion eCOA enables you to run decentralised clinical trials with patients participating remotely, using eConsent and patient diary for higher compliance
Clinion EDC - AI-enabled and Integrated Electronic Data Capture(EDC) Software
Medidata CTMS - Medidata CTMS seamlessly integrates with Medidata Rave to provide real-time views into study progress without manual tracking.
RTMS - RTMS is an oilfield equipment and rental management solution that provides tools like invoice billing management, purchasing, fixed assets and more.