The Collaborative Institutional Training Initiative (CITI) was founded in March 2000 to develop a web based training program in human research subjects protections. It has grown to include several hundred participating institutions from around the world.

You will need to select a learner group.  See the table below for guidance on which learner groups you will need to select.
Group 1 FDA regulated research: investigational drugs, devices, and biologics.  This learner group must also complete the Good Clinical Practice module.
Group 2 Non-FDA regulated research: prevention/intervention studies, community-based studies, investigator-initiated studies that do not involve the use of investigational drugs, devices, or  biologics.  This learner group may also require completion of the Good Clinical Practice module.
Group 3 Human derived materials research: specimens, human tissue, genetic/reproductive material, medical records, databanks, and registries.  This learner group may also require completion of the Good Clinical Practice module.
Group 7 Social and behavioral research: surveys, questionnaires, interviews, photography, tape recordings.  This learner group may also require completion of the Good Clinical Practice module.
GCP Good Clinical Practice

 *For any questions regarding CITI, please contact our Training Coordinator at 706-721-9630.