Clinevo eConsent is a regulatory-compliant and patient-friendly electronic consent system for clinical trials. Clinevo eConsent is a mobile-friendly electronic consenting system that maintains participant engagement, improves their comprehension, simplifies compliance monitoring, and optimizes the overall quality of the consenting process.
Clinevo eConsent supports multimedia components (audio, video) that may be utilized to create an interactive and engaging informed consent experience, accommodating various learning styles.
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
Clinevo Safety is built on a simplified technology stack, ensuring cost-effectiveness, easy maintenance, and faster user adoption.
Regulatory Inspection Ready
Clinevo eConsent Complies with all current and emerging regulations including 21 CFR Part 11, ANNEX 11, GxP and GDPR.
Anytime, Anywhere & Any device
Clinevo eConsent is compatible with iOS or Android, iPad or laptop or any device.
System Integrations
Clinevo eConsent is built on JAVA technology which enables it to easily communicate with various other CTMS and EDC systems.
Clinevo Pharmacovigilance Software offers intelligent analytics and real-time compliance alerts while ensuring seamless access from anywhere.
Multimedia Training
Cost Effective & High Performing
Clinevo eConsent is built on a committed Infrastructure, hosting, training, business process and 24/7 application support.
