The future of study startup gives sites flexibility, while ensuring total visibility for study teams like yours. Optimize operations across each unique site, with guided configurations to ensure compliance and control.
Streamline participant payments with automated workflows that simplify stipends, reimbursements, and tracking for coordinators, participants, and finance teams.
Discover a research management system that unifies protocols, participant data, and financial processes while ensuring billing compliance.
Unlock actionable research analytics with Insights—turnkey dashboards offering clarity on accrual, timelines, and portfolio performance.
Demonstrate research ROI with EVAL, a tool designed for streamlined reporting and impactful insights for cancer centers and academic institutions.
Streamline regulatory workflows with eReg, a system for managing protocol documents, e-signatures, and seamless sponsor collaboration.
Simplify data management with eSource + EDC, featuring secure audit trails, calendar building, and seamless CTMS and EMR integration.
Enhance consenting with eConsent—streamlined workflows, remote signing, and compliance features to improve study oversight and participant engagement.
Streamline clinical trials with Clinical Conductor CTMS—boost enrollment, enhance communication, and optimize financial and operational efficiency.
Enhance recruitment and retention with CCText—CTMS-integrated two-way texting for streamlined outreach, appointment reminders, and consent scheduling.
Streamline participant reimbursements with instant, CTMS-integrated payment solutions designed for efficiency, accessibility, and participant satisfaction.
Improve Efficiency and Get the Most From Your Resources Designed to maximize resource utilization, the Biopoint Treatment Scheduler helps ensure
