Accelerate Your Research Operations

Trusted by tens of thousands of research sites, institutions, academic medical centers, cancer centers, and health systems, Advarra streamlines study activation while increasing compliance and operational efficiencies.  

Designed to optimize workflows across all types of sites, we provide services and solutions in: 

• Institutional review board (IRB)
• All major therapeutic areas and research phase, with specialized services for Phase I, oncology, and more
• Turnaround time: four business days for protocol reviews; one business day for site reviews
• Institutional biosafety committee (IBC)
• Data monitoring committee (DMC)
• Endpoint adjudication committee (EAC)
• Consulting 
• HRPP resource and project support
• HRPP health check
• Support with applications for accreditation
• Policy/standard operating procedure gap analysis and development
• Professional Services
• Streamline your study activation with budget negotiation, informed consent development, coverage analysis, custom eLearning, and more

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