IRB Overview

Our IRB Services were founded with the goal of transforming the IRB industry by placing a strong focus on customer service, ethics, and innovation.

At Sitero, we uphold a culture that places a high value on maintaining the integrity of science and conducting research in an efficient and ethical manner. We take pride in our ability to deliver exceptional service through a single point of contact, responsive boards, and fast turnaround times that are competitive in the industry. This approach has earned us a solid reputation for outstanding performance, enabling us to establish partnerships with renowned experts across various therapeutic areas.

Regardless if you’re an CRO/Sponsor who needs to have ethical, efficient review services, an investigator who has a question, or an institution who wants to develop synergies in their IRB operations, we can help. Our IRB comprises recognized experts in their respective fields. Our team boasts over 50 years of collective IRB experience, and our IRB Board possesses expertise in safeguarding the well-being of human subjects.

Accreditation and Compliance

Sitero IRB is organized and operates in compliance with the US federal regulations (including, but not limited to 21 CFR Parts 50 and 56, and 45 CFR Part 46), various guidelines as applicable (including but not limited to OHRP, FDA, EPA, ICH GCP as specific to IRB review, and the ethical principles underlying the involvement of human subjects in research (including The Belmont Report, Nuremberg Code, Declaration of Helsinki).

Sitero IRB is registered with FDA and OHRP

  • IRB Organization (IORG) Number: 011484

  • IRB Registration Number: 00013619
    (expiration date: 09/16/2025)

  • Federalwide Assurance (FWA) Number: 00032739
    (expiration date: 09/28/2027)

Please note that the IRB registration number applies for both FDA and OHRP registrations.