Welcome to the Advarra IRB Training Portal

After you have created your submission in CIRBI, you can check its progress, review details, or provide clarifications if needed. This module walks you through how to locate your submissions, explore the information available in the submission workspace, and respond when action is needed. Read more

In this module, learn more about how to manage staff on protocols within CIRBI.  You will also learn more about managing notifications for your staff and yourself.    Note: This module reviews basic functionality. Details of forms, fields, or other features may differ in your instance of CIRBI. Read more

In CIRBI, it’s easy to keep your protocol contacts and notification preferences up to date, ensuring the right people have access to submissions and receive real-time updates. User access and targeted alerts help you manage submissions efficiently throughout the review process. Read more

In this module, learn more about submitting modifications and reporting safety events in CIRBI.   Note: This module reviews basic functionality. Details of forms, fields, or other features may differ in your instance of CIRBI. Read more

After a protocol or site submission is approved, additional submission options, such as modifications and safety event reports, become available. This module explores how to submit those two specific types of submissions for the approved protocol or site. Read more

Human Subjects Protection (HSP) training is essential for investigators and research staff. HSP training describes how investigators, sponsors, and IRBs work together to protect the rights, safety, and well-being of subjects on clinical trials.  HSP training aims to ensure that: the rights, safety, and well-being of human subjects are protected privacy and confidentiality of human subjects in research are maintained View each video to learn more about different topics in HSP.  To pass this course, you must complete the assessment with a score of 80% or greater.    Read more