Training Videos, Modules, and Courses
 

• Introduction to the Institutional Review Board (IRB) Process [HTML Video, 04:48 minutes]
• What Needs IRB Review? [HTML Video, 05:10 minutes]
• Working with the IRB/ORI: Processes and Best Practices, 2023 CCTS Session [HTML]
• Research Recruitment and Advertising in Human Research [HTML, ~15 minutes]
• NEW - UK ORI Informed Consent Process Interactive Course [HTML]
• Waiver of Consent vs. Waiver of Consent Signatures [HTML Video, 04:15 minutes]
• Faculty Advisor Responsibilities [HTML Video, 05:02 minutes]
• A Mentor’s Guide to the IRB: A Faculty Advisor Workshop [Video, 44:22 minutes]
• Submission Tips in Under 10 Minutes [HTML Video, 09:25 minutes]
• The Short Form Consent Process for Non-English-Speaking Participants Overview [HTML Video, Video 06:38 minutes]
• Use of Gender-Inclusive Language [HTML Video, 05:41 minutes]
• Remote Informed Consent [HTML Video, 08:51 minutes]
• Real World Data [HTML Video, 07:30]
• Don't Destroy Data [HTML Video, 03:11]
• HIPAA at UK [HTML Video, 04:27 minutes]
• Association for the Accreditation of Human Research Protection Programs (AAHRPP) Interactive Training [HTML]

Interactive Tools
 

• UK ORI Interactive FDA Flow Chart: Medical Device Trials [HTML Interactive Tool]
• UK ORI Interactive FDA Flow Chart: Drugs/Biologics Trials [HTML Interactive Tool]
• Primary Research & Future Use [HTML Interactive Tool]
• UK ORI Secondary Use Research Tool [HTML Interactive Tool]
• New to the UK Institutional Review Board (IRB) process? [HTML Interactive Tool]
• Short Form Consent Process Frequently Asked Questions (FAQs) [HTML Interactive Tool]

• UK ORI Dictionary of IRB and Human Research Terms [HTML Interactive Tool]

• Federal Regulation Tracker [D86.0000] [HTML Interactive Tool]
• HSP or RCR? [HTML Interactive Tool]
• Research vs. Quality Improvement [HTML Interactive Tool]
• Exempt Review Decision [HTML Interactive Tool]

Other Training Courses or Content
 

• Single IRB Reliance Training for Investigators [HTML]

• ORI Non-UK Human Subject Protection Course [HTML]

• K-12 Teacher & Support Staff Human Subject Protection Training [HTML]

• Good Clinical Practice Training for Sponsor-Investigators on FDA-regulated research [HTML]

ORI Frequently Asked Questions (includes IRB, RCR, etc.)

Outreach & Events

Webinars

• CITI Optional Courses [HTML]

OHRP Education Resources & Videos

• Videos by Topic [HTML]
• Revised Common Rule Materials & Videos [HTML]
• Mini-Tutorial Series [HTML]
• Educational Resources for IRB Members [PDF]
• Educational Resources for IRB Administrators and Staff [PDF]
• Educational Resources for Investigators [PDF]

Sample Applications and Protocol Development Resources

Human Research Q&A Guide

Human Research Training Materials