Training Resources
- CITI Collaborative Institutional Training Initiative
- Human Participant Protections Education for Research Teams (free from NIH)
- Human Subjects Research program at the Department of Energy
- PRIM&R Educational Programs
- Clinical Device Group
- Office for Human Research Protections (OHRP) Education
- Responsible Conduct of Research Education Committee (RCREC)
- NIH's Bioethics Resources on the Web
- Ethical Issues in Research Involving Human Participants
Ethical Principles and Codes:
- President's Council on Bioethics
- National Bioethics Advisory Commission
- Belmont Report: Ethical Principles and Guidelines for the Protection of Human Subjects of Research
- Nuremberg Code
- World Medical Association Declaration of Helsinki
- International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH)
- Guidelines for Good Clinical Practice
- ICH Considerations for Clinical Trials
- Recommended Council Guidelines on Ethyl Alcohol Administration in Human Experimentation - NIAAA
Department of Health and Human Services
- Office for Human Research Protections (OHRP)
- Protection of Human Subjects 45 CFR 46
- Office of Human Research Protections - Assurances
- Office of Biotechnology Activities
- DHHS IRB Member Guidebook
- NIH Home Page
- International Laws, Regulations and Guidelines Related to Human Subject Research Protections
- Certificate of Confidentiality Information
Food and Drug Administration:
- FDA Information Sheets and Guidance for Institutional Review Boards and Clinical Investigators
- Protection of Human Subjects 21 CFR 50 - US FDA
- Institutional Review Boards 21 CFR 56 - US FDA
- Code of Federal Regulations
Veterans Administration:
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