IRB solutions to safeguard research participants

Regardless of your project’s scope, therapeutic niche or number of investigators, Advarra® is your partner in the conduct of efficient, responsible research. By giving you faster access to information, easier record management and secure communication tools, Advarra reinforces high-integrity study conduct and regulatory compliance, all while streamlining the way your team communicates.


For pharmaceutical, medical device and diagnostic product developers, Advarra provides expert guidance across all major therapeutic areas.

Institutions, AMCs and Research Consortia

Advarra has assisted more than 3,100 institutions, hospitals, and AMCs for everything from single investigational sites to multiple site research consortia and therapeutic networks.

Investigators and Site Networks

Dedicated coordinators, real-time reporting and web-enabled technologies support transparent and efficient review, simplifying collaboration.

Canadian Review

Advarra has boards in Ontario and Quebec that handle all your Canada-specific review needs.

Need more information on working with the IRB? Read our FAQ.

Ready for Solutions That Are Altogether Better?

Tell us what you’d like Advarra to do for your research program.