Skip to main content

Human Subjects Research

Research Integrity and Compliance serves as the University point of contact for the different IRBs that review human subjects research against federal regulations and ethical standards. For questions about which IRB to use, assistance with a unique case, or questions about accessing VUMC clinical resources, please contact ric@vanderbilt.edu.

 

VUMC IRB

The Vanderbilt University Medical Center (VUMC) Human Research Protections Program (including the IRB) reviews most VU studies. See the tip sheet for VU researchers (under ‘Guidance’) for the difference between informed consent and an information sheet; the definition of “engaged” in research; the difference between recruitment and screening; the difference between non-research and research projects, an overview of the single IRB process, information on conducting research in schools, and HRPP resources. Call the VUMC IRB with questions.

 

BRANY IRB for International Studies

BRANY is an independent IRB that reviews all VU research studies with an international component that do not include

  • VUMC Key Study Personnel (KSP)
  • resources owned or shared by VUMC
  • funding transferring through VUMC
  • data transferring to VUMC,
  • nor HIPAA protected data.

If your international study includes any of the above items, it will be reviewed by VUMC IRB. See more on the criteria and instructions for submitting studies to BRANY. 

 

VU Social, Behavioral, and Educational Research IRB

VU is in the early stages of establishing a Social, Behavioral, and Educational Research (SBER) IRB (see MyVU article). The effort is being led by a faculty committee and with support from VU stakeholders and our partners at VUMC.

 

Access to VUMC Clinical Resources

Vanderbilt University researchers may need access to VUMC clinical systems, facilities or patients to complete research projects. If you are faculty, staff, a postdoc or a graduate student, check eligibility and request access to VUMC Clinical Resources.