Technology to Streamline Your Research Program
Oversee and execute global studies, ensure compliance through study-specific training and schedules, monitor site progress, and expedite IRB submission and review with our integrated and secure technology solutions for sponsors and CROs.
Our Solutions Empower Clinical Research Leaders
Technology Solutions Proven to Reach Your Milestones Quickly and Compliantly
When managing a large research program that spans continents and cultures, ensuring efficient and compliant research is critical to success. Advarra’s technology solutions for sponsors and CROs streamline key processes to keep your study teams, site staff, and participants compliant, connected, and moving forward.
Unite Site Staff, Participants, and Study Teams
Ensure compliant and confident execution of the protocol, empower and inform study participants, and efficiently manage and monitor complex studies within one intuitive platform.
Centralize and Simplify IRB Management
Enable real-time status reporting and direct communications with the IRB for more transparent access and oversight of your clinical research programs with the Advarra Center for IRB Intelligence (CIRBI) Platform.
Automate and Streamline Document Management
Securely transfer your IRB documents and data directly into your electronic trial master file (eTMF) via Advarra Connect, powered by the Advarra CIRBI Platform.
Simplify Study Startup and Ensure Site Performance
SiteIQ, formerly Performance Data Quicklist (PDQ), is a powerful asset for study planning, helping sponsors and CROs simplify study startup and gain unparalleled insights into site performance. SiteIQ also enables sites and institutions to highlight their expertise and increase visibility with sponsors and CROs.
Accelerate Study Startup
Condense the time it takes to obtain IRB review for numerous sites and enable rapid onboarding for sites with Advarra’s IRB-Ready capabilities.