Track Your Protocols with ProIRB®

Imagine the ability to track every piece of paper that crosses your desk! Your Agenda and Meeting Minutes are built for you, according to the regulations and your policies!

Some Additional Features

Track Consent Form revisions, create Reviewer Checklists, Obtain reports as to the number of studies within risk/ benefit/ vulnerable population/ child and other categories.

Adverse Events: Easily track internal/ external Adverse Events, IND and Medwatch #ís! Determine what protocols are using the same drug or combination of drugs.

Custom Continuing Review, IRB Action and many other letters created, merged, sent and tracked with ProIRB®! Our Follow-Up Manager is your own tickler-system reminding you of outstanding issues!

Track the education/ certification of your PI's, Board Members and Study Coordinators.