Product Overview
Clinevo eConsent is a regulatory-compliant, patient-friendly electronic consent system for clinical trials. It works seamlessly on mobile devices, keeping participants engaged while helping them better understand the study. The system also simplifies compliance monitoring and improves the quality of the consent process.
Clinevo eConsent includes multimedia features like audio and video. These tools create a more interactive experience and support different learning styles.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
One Clinical Trial Platform: One interactive platform with EDC, IWRS, eCOA, CTMS, eTMF, and Remote Monitoring capabilities combined.
Decentralized & Hybrid Studies: Clinevo eConsent enables seamless support for decentralized and hybrid Clinical Trials.
Simple to Use: Clinevo eConsent has a simple design and user interface that makes it easy for participants to understand and use the application with little or no training.
Improved Compliance: Clinevo eConsent Alerts are delivered directly to participants' smartphones to remind them to complete the tasks, hence increasing compliance.
About the company
Founded in 2016, we are a Software Development Company specialized in developing and implementing robust technology solutions for Life Sciences R&D. We help Pharma, Biotech and CROs in reducing their time and cost in Clinical trials by implementing innovative technologies that involves Data warehousing, Analytics, Collaboration, Automation, and Artificial Intelligence.
With our unique combination of domain experience & technology expertise, we are committed towards delivering the most efficient and the best practical end-to-end software solutions with HIPAA, GXP, CSV, 21 CFR Part 11 and other applicable regulatory guidelines. Our unmatchable domain experience and technology expertise enables us to deliver the best software solutions.
