Section 3701:1-58-04 - Provisions for the protection of human research subjects(A) A licensee may conduct research involving human research subjects only if it uses the radioactive materials specified on its license for the uses authorized on its license.(B) If the research is conducted, funded, supported, or regulated by a federal agency that has implemented the federal policy for the protection of human subjects as specified in 45 C.F.R. Part 46(as in effect on the effective date of this rule), the licensee shall, before conducting research:(1) Obtain review and approval of the research from an "institutional review board," as defined and described in the federal policy; and(2) Obtain "informed consent," as defined and described in the federal policy, from the human research subject.(C) If the research will not be conducted, funded, supported, or regulated by a federal agency that has implemented the federal policy, the licensee shall, before conducting research, apply for and receive a specific amendment to its medical use license. The amendment request must include a written commitment that the licensee will, before conducting research:(1) Obtain review and approval of the research from an "institutional review board," as defined and described in the federal policy, and approved by the office of human research protection; and(2) Obtain "informed consent," as defined and described in the federal policy, from the human research subject.(D) Nothing in this rule relieves licensees from complying with the other requirements in this chapter.Ohio Admin. Code 3701:1-58-04
Effective: 4/17/2022
Five Year Review (FYR) Dates: 1/31/2022 and 04/07/2027
Promulgated Under: 119.03
Statutory Authority: 3748.02, 3748.04
Rule Amplifies: 3748.04
Prior Effective Dates: 08/15/2005, 10/04/2010, 08/10/2015