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 - Clinical Trial Management Software (CTMS) gives enhanced visibility into all aspects of the clinical trial process - from study plan, Remote monitoring, and Clinical data management
Accelerate Trials Clinion CTMS is an Integrated Clinical Trial Management Software that allows users real-time visibility across the study spectrum, allowing for real-time interventions and course correction, leading to accelerated study timelines
Reduced Trial Costs Customized workflows, pre-set processes, real-time status reports, automated alerts, real-time monitoring, holistic visibility – result in immediate and sustained efficiencies to reduce trial costs significantly.
Enhanced Visibility Real-time Integration gives enhanced visibility into all aspects of the clinical trial process - from study plan, design, site selection, subject recruitment, data capture, monitoring, remote monitoring, drug allotment, Inventory management and data management.
Feature-rich and Versatile Clinion CTMS Software manages a large part of clinical trial operations. Moreover, it is constantly evolving, adding new features and modules almost daily, making it more versatile and user-friendly for its users.
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 eCOA - Clinion eCOA enables you to run decentralised clinical trials with patients participating remotely, using eConsent and patient diary for higher compliance
eReconciliation - eReconciliation is a software that allows users to compare records of data from any clinical and safety database and informs users if there is any change.
IQVIA - IMS Health and Quintiles are now IQVIA.
Protocol Manager (CTMS) - Protocol Manager (CTMS) is a clinical trial management system that helps users to manage clinical operations and trials of drugs and vaccines in all the phases.
Medrio ePRO - Improve compliance and stay better attuned to patient experience with Medrio’s innovative web-based ePRO platform.
EtQ Reliance - QMS integrates data to reduce risk and ensure compliance.