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.

Expertise

The Advarra advantage begins with something essential: experience. 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 biosafety.

We have the resources and experience to help you navigate the ethical, legal, and regulatory risks associated with complex, far-reaching studies, paired with the agility required to meet your study’s unique needs.

One-Touch Collaboration

With Advarra’s One-Touch Collaboration, your research team benefits from an outstanding service experience, a single point of contact, and consistent reviews from our integrated, single IRB. It is our goal to proactively facilitate your study experience and deliver unmatched support. Benefits include:

  • One central point of contact who knows you and your study(ies)
  • One stream of clear, coordinated communications
  • One study startup process for all sites, whether an institution or an independent research site
  • One set of forms, processes, and document templates for clear document management

Unlike other IRBs, Advarra offers a truly single IRB review and delivers white-glove service to our clients. We also guarantee an outstanding, streamlined process from submission to final documentation.

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.

Regardless of project size or scope, you’ll experience collaboration without complexity to guide your research to the highest ethical standards.

The Advarra Advantage

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review without roadblocks
compliance without complication
compliance without complication
technology without turmoil