Human Research Protections Office (HRPO) and Institutional Review Board (IRB)
Welcome to Carilion Clinic's Human Research Protections Office (HRPO) and Institutional Review Board (IRB).
Use the information on these pages to help you navigate your research study and the PRIS3M Submission System. We're also available for consultations. Please feel free to reach out to us at irb@carilionclinic.org for any inquiries you have or assistance you need. Your questions are important to us, and we're here to support you and your team in your research endeavors.
Getting Started
When considering submission of a research study to the Carilion's Human Research Protections Office (HRPO) and Institutional Review Board (IRB), understanding the initial requirements is essential. This guidance document for new investigators will optimize your submission and enhance efficiency. The HRPO team is committed to supporting investigators and research teams throughout the review process.
Principal Investigators and Research Teams
Use the resources for information on submitting a new research application and accessing resources for our PRIS3M online submission system, as well as helpful guidance and templates for your submission.
Researchers Support and Education Center
Learn more about support services, such as contact information for the HRPO staff, list of our standard operating guidelines and educational resources.
For Research Participants
Are you interested in learning more about being a research participant? This section will provide you with more information about the experience of being a research participant, FAQs about research and helpful links to learn more about clinical trials at Carilion and beyond.
Institutional Review Board Members
Find out more about our IRB members, for the IRB meeting schedule and for helpful resources for board members.
