38 CFR Part 16
23 sections.
- § 16.101To what does this policy apply?
- § 16.102Definitions for purposes of this policy
- § 16.103Assuring compliance with this policy—research conducted or supported by any Federal department or agency
- § 16.104Exempt research
- § 16.105-16.106[Reserved]
- § 16.107IRB membership
- § 16.108IRB functions and operations
- § 16.109IRB review of research
- § 16.110Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research
- § 16.111Criteria for IRB approval of research
- § 16.112Review by Institution
- § 16.113Suspension or Termination of IRB Approval of Research
- § 16.114Cooperative Research
- § 16.115IRB Records
- § 16.116General Requirements for Informed Consent
- § 16.117Documentation of informed consent
- § 16.118Applications and proposals lacking definite plans for involvement of human subjects
- § 16.119Research undertaken without the intention of involving human subjects
- § 16.120Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency
- § 16.121[Reserved]
- § 16.122Use of Federal funds
- § 16.123Early termination of research support: Evaluation of applications and proposals
- § 16.124Conditions
This is legal information, not legal advice. Laws vary by jurisdiction and change frequently. Always verify current law with official sources and consult a licensed attorney in your jurisdiction for advice on your specific situation.