About the IRB office and IRB staff


EVMS currently has two internal IRB's.  The "1st Thursday" IRB and the "3rd Tuesday" IRB both oversee Biomedical and Social Behavioral research.  Each IRB holds their convened meetings on their respective meeting dates (noted by the name of the Board) each month at 8:30 a.m.  Protocols requiring convened Board review are assigned to meetings on a first come, first served basis after the submission is verified as complete by the ORSP/IRB office.  

In addition to the convened meetings, the IRB's have sub-committee meetings that are held on the same meeting dates.  The sub-committee reviews exempt and expedited studies.  Requests for "Not Research" and "Not Human Subject Research" determinations are made by the ORSP/IRB staff who may consult with IRB members as needed.



Many of the EVMS ORSP staff are Certified IRB Professionals (CIP).  Certification is overseen by a national leader in research ethics, Public Responsibility in Medicine and Research (PRIMR).  Staff members also have varying backgrounds, including pharmaceutical regulatory management, post-graduate degree in science, graduate degree in public health, administration of a research unit in clinical practice, and over 40 years of direct IRB experience.

Oversight of the office is provided by the Assistant Dean for Human Subjects' Protections.


The Office of Research Subjects' Protections offers presentations on many topics to help investigators and research team members understand the IRB process and requirements.  If you are interested in having a presentation made to your department or group please contact:

Harry J. Tillman, RN, PhD, CIP
Educational Specialist, Protocol Development
TillmaHJ@evms.edu or 757.446.7073