Institutional Review Board (IRB)
Who we are
Georgia State University’s Institutional Review Board will apply these tenants to all human subjects research, regardless of funding.
IRB Drop-in Help
When: Every Wednesday from 3:15 – 5:15 p.m., September 9 – December 2, 2015
NOTE: Drop-in for November 11th has been cancelled and will resume on November 18th
Where: Suite 217 Dahlberg Hall
Appointments: Faculty will be served on a first-come-first served basis during these times
The Office of Human Research Protection offers personalized, one-on-one guidance for investigators provided by the Georgia State University IRB. Help is provided with responses to revisions, formulating complicated human subject protection plans, and international research protocols.
Georgia State University works diligently to maintain compliance with all federal regulations impacting the rights and welfare of human subjects participating in research. The Family Educational Rights and Privacy Act (FERPA) is a federal law that gives parents certain rights with respect to their children’s educational records. These rights transfer to the student when he or she reaches the age of 18 or attends a school beyond the high school level.
To stay in compliance with FERPA, it is necessary for researchers at GSU to meet new requirements in their IRB applications. If you conduct human subjects research that will involve data from student educational records such as class work, grades, attendance records, communications, projects, classroom tests, standardized tests, journals, or SAT/ACT scores, even if this information is from your own classes or students, this correspondence is applicable to your research endeavors. Guidance on IRB requirements and how FERPA regulations impact your research can be found at: www.gsu.edu/irb/ferpa.
Implementation of FERPA guidelines is effective July 15, 2015.
Changes to Model Informed Consent Form
A new Compensation Section has been added to the model informed consent form. All new submissions must use the new version of the model informed consent. Please see the following link to access the model informed consent form: http://ursa.research.gsu.edu/repo/modelInformedConsent.docx
New Form in iRIS for Authorization Agreements
Authorization agreements are used when one institution relies on the review of another institution’s IRB. If you wish to have an authorization agreement in place, a new form is available in iRIS.
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- Application Assistance
- IRB Manual [PDF]
- Human Subjects Powerpoint Presentation [PPT]
- Model Consent Form [Word]
- Becoming a Research Volunteer: It’s Your Decision (from hhs.gov) [PDF]
- Ser Voluntario en Estudios Clinicos: Es Su Decision (de hhs.gov) [PDF]