Study Lifecycle Management offers end-to-end solutions to streamline clinical research operations efficiently and securely. With Site, Study/Project, and Participant Management, every phase—from planning to post-study analysis—is optimized through real-time tracking, automated notifications, and seamless reporting, ensuring protocol compliance and transparency. The eConsent feature modernizes the informed consent process with secure, user-friendly digital workflows, enabling participants to review and sign forms remotely while adhering to global regulatory standards. Together, these tools enhance collaboration, compliance, and participant engagement across the entire research lifecycle.