Kan. Admin. Regs. § 28-70-4, Confidential data for follow-up patient studies

Establishes standards and procedures for obtaining data for follow-up cancer studies. Requires researchers to submit research proposals to their institutional review board, the cancer registry data release board, the Department of Health and Environment’s institutional review board, and the university of Kansas medical center’s institutional review board. Requires the cancer registry director to obtain informed consent from individuals before releasing their information for research purposes.