eConsent Demo Request
Enhance consenting with eConsent—streamlined workflows, remote signing, and compliance features to improve study oversight and participant engagement.
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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
Simplify study startup with an IRB reliance agreement that defines roles, ensures compliance, and prepares your institution for streamlined oversight.
Explore IRB review essentials for Phase I research, including protocol expectations and critical informed consent topics for successful approval.
Simplify your grant application with sIRB support documents tailored to meet requirements for NIH and other federally funded multisite research.
Explore Advarra’s extensive network of over 3,500 institutions, ensuring streamlined IRB partnerships for your clinical research needs.
Access the latest IRB roster with ease via CIRBI’s reference materials or request a copy to be sent directly to your email.
Learn more about Advarra’s IRB services or log in to CIRBI for study-specific updates and streamlined information requests.
Enhance resource efficiency and patient access with Biopoint Tracker, a versatile tracking solution for surgery, pharmacy, radiology, and more.