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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.

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 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.

Biopoint Tracker Demo Request

Enhance resource efficiency and patient access with Biopoint Tracker, a versatile tracking solution for surgery, pharmacy, radiology, and more.

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