U.S. Department of Health and Human Services

• Compilation of Guidances on the EU General Data Protection Directive (GDPR)
• DHHS Regulations
• DHHS Policy and Guidance
• ORI (Office of Research Integrity)
• Belmont Report  
• Investigator Manual (Appendix A-1: Additional Requirements, DHHS-Regulated Research) 

U.S. Food and Drug Administration

• FDA Regulations
• Clinical Trials Guidance Documents 
• Investigator Manual (Appendix A-2: Additional Requirements, FDA-Regulated Research) 

International Conference on Harmonisation - Good Clinical Practice

• ICH-GCP Website
• Good Clinical Practice standards 
• Investigator Manual (Appendix A-3: Additional Requirements, Clinical Trials (ICHGCP)

Veterans Administration

• VAMHCS Collaborative Studies Checklist
• VA — Maryland Research and Development
• VA — Current ORD Policy Documents
• VA Regulations - Human Subjects Protections
• Office of Research Oversight (ORO) - Veterans Health Administration 
• Investigator Manual (Appendix A7: Additional Requirements, VA Research) 

Department of Defense (DoD)

• DoD Directive (DoDD) 3216.02 — Protection of Human Subjects and Adherence to Ethical Standards in DoD-Supported Research
• Department of the Navy (DON) — Human Research Protection Program

Other Resources

• NIH (National Institutes of Health)
• NIH Certificates of Confidentiality (CoC)
• AAHRPP — Association for the Accreditation of Human Research Protections Programs
• ACRP — Association of Clinical Research Professionals
• AAMC Research Compliance Resources
• Barnett Educational Services
• PRIM&R
• The Hastings Center
• SOCRA — Society of Clinical Research Associates
• Center for Clinical Trials
• General Clinical Research Center
• Certificates of Confidentiality
• Bioethics Resources