Meet Sterling IRB
For 30 years, Sterling IRB has helped lead the way in protecting the rights and welfare of clinical research participants and providing the regulatory expertise needed for quality reviews. We serve pharmaceutical and biotechnology companies, CROs, federal agencies and individual investigators, as well as acting as the review board for studies conducted at hospitals or academic institutions.
With a top priority on responsiveness and a single point of contact readily available, Sterling IRB protects the integrity of your research while uncomplicating compliance. From early phase studies to Phase IV trials, Sterling’s experts work diligently with you to provide comprehensive IRB solutions, across the board.
The review boards are comprised of highly qualified individuals representing a variety of scientific and nonscientific disciplines.
Sterling is a proud member of the National Veteran Business Development Council (NVBDC).
Where Integrity Is Indispensable.
At Sterling IRB, we believe integrity is an essential component of a strong team. More importantly, it’s one of the characteristics that define our proven approach.
Where Experience Is Essential
At every touch point, you are supported by accomplished, experienced individuals who understand the issues that are most important to you.
Where Compliance Isn’t Complicated
We’re driven to provide personalized service to ensure accurate, timely results, and superior regulatory guidance.
It’s our mission to protect the integrity of clinical research in the U.S. and Canada. Sterling IRB gives you the attention to detail needed to safeguard your trial.
Find out why more companies choose Sterling as their IRB.