IRB management simplified

Let IRBANA help you stay on top of the complex and time-intensive efforts to ensure compliance with federal regulations for the protection of human subjects.


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Electronic submissions

easily enter IRB submissions for new study approval, continuing review, revisions/amendments, key personnel changes, etc. including document upload

facilitates communication between researchers and IRB staff

automatic email notifications for approval process status updates

Manage protocols

capture protocol details including status

track IRB review dates and actions including amendments and revisions 

document storage and access

key personnel tracking with license/training management



Agenda, Minutes and Approval Letters

create IRB meeting agenda automatically based on customizable design

easily separate submissions into appropriate sections based on type of submission, type of review, and other criteria

create meeting minutes, update actions and record voting in seconds

store approval letter templates and quickly generate letters in Word or PDF format


Comprehensive reports

protocol status, continuing review and expiring study dates

custom reports built at no additional cost

IRB Reviewers

email notification when protocols/documents ready for review

one-screen display of all protocols and documents for your review

record comments directly into IRBANA

notify IRB staff automatically when review has been completed


invoicing, payment tracking and allocation

easily separate fees by type of review (e.g. Full Board or Expedited)

track any funds paid out to third-parties

complete reporting


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