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Oklahoma Administrative Code (Last Updated: March 11, 2021) |
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TITLE 310. Oklahoma State Department of Health |
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Chapter 2. Procedures of the State Department of Health |
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Subchapter 31. Human Subjects Protection |
| SECTION 310:2-31-1. General purpose |
| SECTION 310:2-31-2. Scope |
| SECTION 310:2-31-3. Definitions |
| SECTION 310:2-31-4. Incorporations by reference |
| SECTION 310:2-31-5. Conditions of Federalwide Assurance |
| SECTION 310:2-31-6. Authority of IRB |
| SECTION 310:2-31-7. IRB procedures |
| SECTION 310:2-31-8. Training |
| SECTION 310:2-31-9. Compliance and knowledge of local context |
| SECTION 310:2-31-10. Institutional support of the IRB |
| SECTION 310:2-31-11. FDA regulated research |
| SECTION 310:2-31-12. Usage of procedures for allegation of possible misconduct in science |
| SECTION 310:2-31-13. Research Integrity Officer |
| SECTION 310:2-31-14. Whistleblower |
| SECTION 310:2-31-15. Respondent |
| SECTION 310:2-31-16. Deciding official |
| SECTION 310:2-31-17. Responsibility to report misconduct |
| SECTION 310:2-31-18. Protecting the whistleblower |
| SECTION 310:2-31-19. Protecting the respondent |
| SECTION 310:2-31-20. Cooperation with inquiries and investigations |
| SECTION 310:2-31-21. Preliminary assessment of allegations |
| SECTION 310:2-31-22. Conducting the inquiry |
| SECTION 310:2-31-23. The inquiry report |
| SECTION 310:2-31-24. Inquiry decision, notification, and confidentiality |
| SECTION 310:2-31-25. Time limit for completing the inquiry report |
| SECTION 310:2-31-26. Conducting the investigation |
| SECTION 310:2-31-27. The investigation report |
| SECTION 310:2-31-28. Requirements for reporting to ORI |
| SECTION 310:2-31-29. Institutional administrative actions |
| SECTION 310:2-31-30. Record retention |
Note
[Source: Codified 9-13-19]