VDC™ eConsent is an innovative, regulatory-compliant, patient-friendly, remote consent system for clinical trials. VDC™ eConsent automates the patient enrollment process and onboard patients directly into Captivate™ EDC, improving overall consent tracking management, reducing informed consent errors, and easing the administrative burden for sites and study teams. It also enhances the patient experience with easy-to-understand clinical trial information while improving participant compliance and boosting patient engagement.
Speeds Start-up and Studies
- Integrates with Captivate™ EDC, Captivate™ Randomization, and VDC™ eCOA/ePRO for a single-site experience.
- Facilitates guaranteed signature compliance, remote consent monitoring, and site screening metrics.
- Provides global localization capabilities, enabling configuration for multiple languages and regulatory environments.
- Shortens the VDC™ eConsent study and site set-up timeline from months to weeks.