A Dedicated IRB That’s Dedicated to You

Get the Expert Guidance You Need Across the Board

Sterling IRB employees sitting on chairs with a color overlay. Sterling IRB employees sitting on chairs with a color overlay. Sterling IRB employees sitting on chairs with a color overlay. Sterling IRB employees sitting on chairs with a color overlay. Sterling IRB employees sitting on chairs with a color overlay. Sterling IRB employees sitting on chairs with a color overlay.

Personalized Institutional Review Board Services

With a sole focus on delivering efficient, high-quality institutional review board services, Sterling IRB equips you with the expertise and support needed to accelerate your research to market. For 30 years, we have helped lead the way in protecting the rights and welfare of clinical research participants and providing the regulatory compliance consulting needed for quality reviews.

Our Services

Start a Study

Submit a New Study for Review

To submit a new study to Sterling IRB, please log into or request access to our secure web portal, SilverLink.

What Types of Clinical Research Does Sterling IRB Review?

For 30 years, Sterling IRB has served as the institutional review board for studies in every phase and therapeutic area, from Phase I through post-market research. Our board brings scientific and nonscientific expertise to the questions that newer study designs raise, including:

  • AI in clinical research: We look at how AI-powered tools affect informed consent, data privacy, and model transparency, guided by the same established principles we apply to every innovation
    Decentralized clinical trials: We review hybrid and fully decentralized designs, including eConsent and remote identity verification and safety oversight for participants outside traditional sites
  • Nutraceutical and dietary supplement clinical trials: We provide thorough ethical review for products that fall outside traditional drug pathways
  • In vitro diagnostics and medical devices: We support diagnostic, device, biologic, and gene therapy studies, with regulatory consultation to help keep device timelines on schedule
  • Vulnerable populations: We review research involving prisoners, cognitively impaired persons, pregnant women, and children

Whether your study runs at one site or many sites across the U.S. and Canada, you’ll have a dedicated account manager and a board that meets daily, so complex designs get timely, thorough review.

Our Dedication Speaks for Itself

5 Day Protocol Review

24 Hour Site Review

100+ Years Combined Experience

24/7 Expert Support

1 Focus On IRB Services


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