The Human Research Protection Office is pleased to announce a new consultation program to provide researchers and their team members in-depth protocol-specific guidance about the IRB review process.
Upon request for a consultation, you will be matched with an individual within HRPO who has the appropriate expertise specific to your area of research. HRPO can provide guidance on regulatory requirements, institutional policies, and ethical considerations as it relates to the IRB review of human subject research.
This program will complement the existing HRPO support services. To request an IRB consultation, visit the HRPO Help Services page.