By unifying an extraordinary breadth and depth of IRB regulatory compliance and human subject protection expertise with a client-centric service model, Advarra® provides innovative solutions performed with exceptional quality. That’s why leading sponsors, CROs, academic medical centers and other institutions insist on partnering with Advarra to help advance better research.

Trust Advarra’s integrated solutions and collaborative approach to make your research altogether better.


The Advarra advantage begins with something essential: experience. IRB reviewers and operational staff include distinguished scientists and industry leaders with a deep understanding of and appreciation for the regulatory and scientific framework in which you work.

In addition to providing deep expertise across all major therapeutic areas, Advarra continues to pioneer highly specialized review services for areas such as oncology, neurology and commercial biosafety.


The experts at Advarra are also adept at reviewing studies with your greater research program in mind to support compliant studies now and in the future. Through proprietary technologies and dedicated client services teams, Advarra simplifies submission, tracking and review processes while keeping you aware of real-time progress.

One central point of contact is assigned to every project to help navigate the review approach process. Regardless of project size or scope, you’ll experience collaboration without complexity to guide your research to the highest ethical standards.

The Advarra Advantage

proof point graphic background
review without roadblocks
compliance without complication
compliance without complication
technology without turmoil