IRB Services
Institutional Review Board (IRB)
Advarra’s IRB offers expert guidance, supporting more than 3,500 institutions, academic medical centers, and site networks. From federally-funded to industry-sponsored trials, Advarra provides a comprehensive review service that is flexible, reliable, and easy to integrate with local IRB operations.
Key Features
- Responsive support team
- Dedicated point of contact
- New study review in 4-5 days
- Real-time reporting
- No submission deadlines
IRB Solutions to Empower Research
Comprehensive Review Services
Whether for minimal risk or multisite studies, Advarra’s IRB offers a streamlined process with rapid review timelines and dedicated support for institutions.
Advanced IRB Technology
The Advarra Center for IRB Intelligence (CIRBI) platform enhances communication and offers real-time status updates, enabling faster site activation and efficient decision-making.
Integrated Operations
Advarra’s solutions allow seamless integration between our CIRBI platform and local IRB offices, providing real-time notifications and document tracking.
Dedicated Support
Each client receives a knowledgeable single point of contact at no additional charge to help ensure compliance and timely project execution across all studies.
Therapeutic Expertise
With specialized teams in oncology, neurology, and other therapeutic areas, Advarra’s IRB is equipped to handle diverse, complex studies.
Flexible Options
Rely on experienced institutional research professionals to ensure local context requirements, deferral relationships, and other custom needs are appropriately addressed.
Turnaround Times
days
New protocol and consent (full board review)
days
New protocol and consent (minimal risk review)
days
New site for a multisite study
Turnaround time is dependent on the complete and accurate submission of study documents. Any required follow-ups may extend this timeline.
