CIRBI Submissions

The Center for IRB Intelligence (CIRBI™)

Chesapeake IRB launched a one of a kind web-based management system (CIRBI) that allows sponsors, CROs and investigators to electronically submit and track all IRB-related study documents from initial submission to study close-out.

CIRBI has been independently audited and determined to be compliant with applicable FDA requirements, including 21 CFR Part 11.

Submission and delivery of all study documents is via secure encrypted closed web site.  Available 24 hrs/day, 7 days/week.

To register for CIRBI access, go to www.cirbi.net and select “Sign Up.”

If you would like to participate in a CIRBI Webinar, please contact us at (410) 884-2900.