Any systematic investigation (including pilot studies, program evaluations, and qualitative research), that is designed to develop or contribute to generalizable (scholarly) knowledge, and which uses living humans or identifiable private information about living humans qualifies as human subjects research.
Our regulatory affairs team provides centralized assistance for CCR’s clinical trials and will prepare and submit all Institutional Review Board (IRB) applications and will keep you up to date on the process.
For more details, please review the Protocol Preparation Checklist at the link below. It was created to help guide investigators on the IRB Application process for their protocol submissions.