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.
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.
Global CRO Drives Study Startup Efficiency
PRA Health Sciences partnered with Advarra to increase the number of sites relying on central IRB review, streamlining startup, and increasing overall study efficiency.
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.
Delivering Efficiency with eTMF and Advarra IRB Integration
Teamwork and leadership from an industry-leading biopharmaceutical company and Advarra accomplish integration with their eTMF.
Simplify Study Startup and Ensure Site Performance
Augment existing site databases, identify high-performing sites, and find additional sites for studies already in progress with our Performance Data Quicklist (PDQ) custom performance analytics, dashboards, and curated site data.