Research Clinics
It is the policy of Atlanta VA Clinical Studies Center (CSC) that ALL research projects involving contact with human subjects must have a "Research Clinic" in the VISTA computer system. The guidelines and procedures described in this SOP must be followed to develop a "Research Clinic."
Read More

Human Studies Analyst
The HSA provides guidance and support with initial and ongoing research projects. Services include assistance with protocol submissions to Emory IRB and R&D Committee, HIPAA requirements, writing of VA Authorization form, Informed Consent Form writing and formatting, modifications, continuing review, and project queries.
Read More

Informed Consent Review
An Informed Consent Form (ICF) is required for all studies except those granted exempt status by the Emory IRB and must be prepared according to the VA/Emory IRB Consent sample. The Human Studies Analyst aids in the preparation of consent forms, helping reduce the number of revisions required before you obtain final approval.
Read More

Training & Education
The CSC provides ongoing training and education to Investigators and Research Coordinators. Training topics include conducting human research studies, VA policies and procedures, other institutional policies, audit preparation, Code of Federal Regulations, and monthly educational meetings for Research Coordinators.
Read More