Castor eConsent brings a new level of efficiency, compliance, and participant engagement to clinical research. Its user-friendly design helps sites easily manage both remote and on-site consent, ensuring clear communication of trial information while reducing administrative burden. By providing features like eSignatures, video calls, and a custom landing page, Castor eConsent empowers participants to make informed decisions and remain engaged throughout the study.
Sponsors gain real-time visibility into enrollment progress, enabling quicker oversight, seamless scaling, and faster decision-making. With Castor eConsent already trusted across more than 100 countries, researchers have consistently seen improved compliance, higher retention, and faster study deployment—some studies enrolled tens of thousands of participants within weeks.
Ready to elevate your clinical trials and streamline consent processes? Download the eConsent Fact Sheet now to see how Castor can help you transform participant onboarding.
