SOP Design, Administration, and Compliance

Accelerate Research Operations with Advarra Services for Institutions

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

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

  • Independent Review Board (IRB)
    • Depend on expertise in every major therapeutic area and research phase, with specialized services for Phase I, oncology, and more
    • Simplify the relationship with a fellow SMART IRB reliance network partner
    • Turnaround time: 4 business days for protocol reviews; 1 business day for site reviews
    • Additional integrated review services available: institutional biosafety committee (IBC), data monitoring committee (DMC), endpoint adjudication committee (EAC)
  • Institutional Research Consulting 
    • HRPP resource and project support
    • HRPP Health Check
    • Support with applications for accreditation
    • Policy/SOP gap analysis and development
    • Training for investigators and other research staff
    • Audit prep and communications with federal authorities
  • Professional Services
    • Increase research productivity with breakthrough efficiencies
    • Streamline your study activation with services like budget negotiation, informed consent development, coverage analysis, custom eLearning, and more
    • Maximize your Advarra technology investments

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Who should watch?

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CEU Credits

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Certificate of Attendance

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Time: 1 p.m. ET, 12 p.m. CT, 10 a.m. PT
Duration: 1 hour

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