IRB: Guidance

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What Types of Activities Require IRB Review
Levels of IRB Review
Ethical Issues in Research
Research Design Guidance
Student Investigators' Guide
Required and Additional Elements of Informed Consent (for non-exempt research)
Informed Consent Process for Exempt Research
IRB Authorization Agreements for Human Subjects Research
Single IRB (sIRB) Review for Multi-Site Cooperative Research 
Assessing Risk Level Using Magnitude of Harm
Human Subjects Research Engagement
Suggested Best Practices for Gender & Sexuality Demographic Questions - from the LU Pride Center for Sexual Orientation and Gender Diversity
International Research and Research with Non-English Speaking Populations - guidance and forms
Changes to NIH Policy for Issuing Certificates of Confidentiality (CoC)
Family Educational Rights and Privacy Act (FERPA)
Unaffiliated Investigators
Data Security and Privacy 
Readability and Comprehension
General Data Protection Regulation (GDPR)
Electronic Informed Consent
Data and Safety Monitoring of Clinical Trials Research
Conducting Research in Schools
Conducting Research Using Crowdsourcing Platforms: Best Practices
Audio and Video Conferencing in Human Subjects Research