The following policies, guidance, and supporting documents ensure that research conducted at Georgia Tech protects the rights and welfare of human research subjects and complies with all applicable laws and regulations.
- Georgia Tech IRB Policies and Procedures Manual
This document sets forth the policies required of all Georgia Tech faculty, staff, and students conducting research that involves human subjects.
- Investigator Agreement for a Clinical Investigation
This agreement is intended for use between Georgia Tech and a PI conducting a clinical trial. The clinical trial agreement sets forth the expectations of the Food and Drug Administration concerning the investigator’s responsibility to (1) supervise a clinical study in which some study tasks are delegated to employees or colleagues of the investigator or other third parties and (2) protect the rights, safety, and welfare of study subjects.
- Atlanta Clinical & Translational Science Institute (ACTSI) Data Use Agreement
As an ACTSI member, Georgia Tech executes data use agreements with other ACTSI partners to facilitate the sharing of de-identified data and limited data sets. GT researchers who are exchanging data with ACTSI partners, Children’s Healthcare of Atlanta, Emory University, or Morehouse School of Medicine, should utilize this Data Use Agreement. Please complete Exhibit A (at the end of the agreement) and upload it to your IRBWISE protocol application.