eSource + EDC Demo Request
Simplify data management with eSource + EDC, featuring secure audit trails, calendar building, and seamless CTMS and EMR integration.
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eConsent Demo Request
Enhance consenting with eConsent—streamlined workflows, remote signing, and compliance features to improve study oversight and participant engagement.
Clinical Conductor CTMS Demo Request
Streamline clinical trials with Clinical Conductor CTMS—boost enrollment, enhance communication, and optimize financial and operational efficiency.
CCText Demo Request
Enhance recruitment and retention with CCText—CTMS-integrated two-way texting for streamlined outreach, appointment reminders, and consent scheduling.
Advarra CCPay Demo Request
Streamline participant reimbursements with instant, CTMS-integrated payment solutions designed for efficiency, accessibility, and participant satisfaction.
Biopoint Treatment Scheduler Demo Request
Improve Efficiency and Get the Most From Your Resources Designed to maximize resource utilization, the Biopoint Treatment Scheduler helps ensure
IRB Reliance Agreement Contact Us
Simplify study startup with an IRB reliance agreement that defines roles, ensures compliance, and prepares your institution for streamlined oversight.
Phase I Contact Us
Explore IRB review essentials for Phase I research, including protocol expectations and critical informed consent topics for successful approval.
NIH sIRB Docs Contact Us
Simplify your grant application with sIRB support documents tailored to meet requirements for NIH and other federally funded multisite research.
IRB Institutional Site List Contact Us
Explore Advarra’s extensive network of over 3,500 institutions, ensuring streamlined IRB partnerships for your clinical research needs.
IRB Roster Contact Us
Access the latest IRB roster with ease via CIRBI’s reference materials or request a copy to be sent directly to your email.
IRB Contact Us
Learn more about Advarra’s IRB services or log in to CIRBI for study-specific updates and streamlined information requests.