IRB: Guidance

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Activities Requiring IRB Review
Assessing Risk Level Using Magnitude of Harm
Certificates of Confidentiality (CoC) - NIH Policy
Conducting Research in Schools
Crowdsourcing Platforms for Conducting Human Subjects Research: Best Practices
Data and Safety Monitoring of Clinical Trials Research
Data Security and Privacy 
Demographic Questions: Collecting Demographic Information from Human Subjects
Electronic Informed Consent
Engagement in Human Subjects Research
Ethical Issues in Research
FDA Regulations for Human Subjects Research
Family Educational Rights and Privacy Act (FERPA)
General Data Protection Regulation (GDPR)
Informed Consent Process for Exempt Research
Informed Consent: Required and Additional Elements (for non-exempt research)
International Research and Research with Non-English Speaking Populations - guidance and forms
IRB Authorization Agreements for Human Subjects Research
Levels of IRB Review
Payments to Research Participants
Readability and Comprehension
Research Design Guidance
ResearchMatch - Recruitment Tool for Clinical / Health-Related Research
Single IRB (sIRB) Review for Multi-Site Cooperative Research 
Student Investigators' Guide
Unaffiliated Investigators
Video Conferencing in Human Subjects Research