SECTION 310:2-31-6. Authority of IRB  


Latest version.
  • (a)   All human subject research will be reviewed, prospectively approved, and subject to continuing oversight by the OSDH IRB.
    (b)   The OSDH IRB will have authority to approve, require modifications in, or disapprove the covered human subject research.
    (c)   Any suspension or termination of approval shall include a statement of the reasons for the IRB's actions and shall be reported promptly to the investigator, appropriate OSDH officials, and the Commissioner.
    (d)   The OSDH IRB will maintain IRB registration under the Office of Human Research Protections to permit the review of federally funded research.
[Source: Added at 36 Ok Reg 1649, eff 9-13-19]