Clinevo eCOA
Clinevo eCOA is regulatory compliant and user-friendly platform that captures outcomes data from patients (ePRO), caregivers (ObsRO), and doctors (ClinRO) with ease and precision. Clinevo eCOA is compatible with iOS or Android, iPad or laptop, and facilitates the execution of Hybrid and Decentralized Clinical Trials.
The integrated Clinevo EDC platform eliminates the need to manage several standalone solutions and streamlines data capture. Participants' data can be collected via digital questionnaires, diaries, or remote devices, and reported and transferred to the centralized EDC system using Clinevo eCOA.


Comprehensive Data Management
Clinevo Pharmacovigilance Software is a powerful, AI-driven drug safety database designed to streamline case processing, ensure compliance, and provide advanced analytics for pharmaceutical companies, CROs, and regulatory teams.
One Clinical Trial Platform
Decentralized & Hybrid Studies
Simple to Use
Improved Compliance
Efficiency and Automation
Clinevo Safety is built on a simplified technology stack, ensuring cost-effectiveness, easy maintenance, and faster user adoption.
Regulatory Inspection Ready
Clinevo eCOA Complies with all current and emerging regulations including 21 CFR Part 11, ANNEX 11, GxP and GDPR.
Anytime, Anywhere & Any device
Clinevo eCOA is compatible with iOS or Android, iPad or laptop or any device.
Real time monitoring, Dashboards and Reporting
Real time monitoring, Dashboards and Reporting
Cost-Effective Solutions
Clinevo Pharmacovigilance Software offers intelligent analytics and real-time compliance alerts while ensuring seamless access from anywhere.
System Integrations
Multimedia Training
Clinevo eCOA is built on a committed Infrastructure, hosting, training, business process and 24/7 application support.
Cost Effective & High Performing
Clinevo eCOA is built on a committed Infrastructure, hosting, training, business process and 24/7 application support.