Hybrid eConsent: Remote And On-Site

Participants who use eConsent consistently demonstrate a better understanding of trial information, leading to higher engagement and a more positive overall experience. Studies show that when participants are more informed and comfortable with the consent process, they are more likely to comply with study protocols, remain enrolled in the trial, and contribute to faster study deployment.

Castor eConsent sets itself apart from competitors by prioritizing flexibility, compliance, and ease of use. Designed to empower clinical trial teams, it simplifies and streamlines the consent process without compromising ethical standards. By enhancing participant comprehension and engagement, Castor eConsent helps researchers optimize trial efficiency while maintaining the integrity of informed consent.