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IRB Submission

If you are not familiar with the IRB Process, please read the information below

 

IRBNet

Log in to the IRBNet Electronic Submission here

 

Beginning Your Research

 

CITI Training and Certification

Before beginning research at Tulane University, each investigator and coordinator should have completed the CITI Training Program.

Take your CITI Training here

 

IRB Review

Types of Review

Before you begin your research, you should be familiar with the types of IRB Reviews  that the HRPO conducts.  Here you will find information on the Initial, Ongoing and Post-Submission processes and what category your potential project may fall into.
 

HRPP Policies and Procedures

Policies and Procedures(pdf)
(html coming soon)

 

HIPAA

HIPAA Authorization Form

HIPAA FAQs for U-D in Research

HIPAA Researcher Certificate

HIPAA IRB Certificate


FWA Assurances

Food and Drug Administration (FDA)

The Belmont Report

Office of Human Research Protections (OHRP)

Code of Federal Regulations

WELCOME


The primary goals of Tulane University's Human Research Protection Office are to balance the protection of human subjects while promoting and facilitating the research enterprise, and to maintain an open and cooperative relationship with the research community. We are committed to assisting you with your various human research efforts.

In addition to the online CITI training course for all research personnel, we publish a newsletter on a quarterly basis. We will also host IRB workshops semi-annually to fulfill a key component of our educational mission. Please check our website regularly as we will be posting information regarding new updates on IRB processes, and timely topics in the news and scientific press regarding human research studies.

Our goal is to provide researchers with a clear view of the IRB submission process. We have created a number of tools including checklists and flowcharts to help you navigate through our processes. Additionally, we have revised our policies and procedures to provide a more succinct framework for the office as we move toward accreditation.

Finally, it is important to note that all IRB approvals must be obtained before beginning any research activity.

The Office will be receptive to your comments and feedback as we strive to make improvements to our policies and procedures. Our aim is to work with you in promoting research involving human subjects at Tulane University.

–The IRB Team

 

Welcome to IRBNet

 

Training Materials

IRBNet Login and Registration Tips

IRBNet Users Guide -
Step by Step Instructions for using IRBNet

IRBNet Electronic Signature Instructions -
Step by Step Instructions on how to Electronically Sign a Submission/Package

IRBNet Electronic Signature Policies
Policies regarding using Electronic Signatures within the IRBNet system

IRBNet Instructions - Researcher 1 (PDF) -
Visual Instructions in Powerpoint on how to submit an Initial Submission/New Project

IRBNet Instructions - Researcher 2 (PDF) -
Visual Instructions in Powerpoint on how to submit Seconday Submissions/Packages and other Advanced Topics

Video Training available here

 

Institutional Review Board, New Orleans, LA 70112 504-988-2665 irbmain@tulane.edu