Oklahoma Administrative Code
Title 310 - Oklahoma State Department of Health
Chapter 10 - Human Subjects Protection [REVOKED]
Subchapter 5 - Compliance With the Registration of the Oklahoma State Department of Health Institutional Review Board [REVOKED]
- Section 310:10-5-1 - FDA regulated research [REVOKED]
- Section 310:10-5-2 - Ethical principles [REVOKED]
- Section 310:10-5-3 - Compliance with 45 C.F.R. Part 46 [REVOKED]
- Section 310:10-5-4 - Authority of the OSDH IRB [REVOKED]
- Section 310:10-5-5 - Informed consent [REVOKED]
- Section 310:10-5-6 - IRB procedures [REVOKED]
- Section 310:10-5-7 - Compliance and knowledge of local context [REVOKED]
- Section 310:10-5-8 - IRB Training [REVOKED]
- Section 310:10-5-9 - Provision of investigator training [REVOKED]
- Section 310:10-5-10 - Institutional support of the IRB [REVOKED]
- Section 310:10-5-11 - Update of IRB Registration [REVOKED]
- Section 310:10-5-12 - IRB membership requirements [REVOKED]
Current through Vol. 42, No. 1, September 16, 2024
Disclaimer: These regulations may not be the most recent version. Oklahoma may have more current or accurate information. We make no warranties or guarantees about the accuracy, completeness, or adequacy of the information contained on this site or the information linked to on the state site. Please check official sources.
This site is protected by reCAPTCHA and the Google
Privacy Policy and
Terms of Service apply.
