Frequently Asked Questions (FAQs)

Institutional Review Board (IRB) FAQs

• General
• IRB Review
• Consent
• Continuation/Annual Administrative Review/Closure

New Researcher FAQs
(includes select information for researchers new to the UK IRB)

Electronic Institutional Review Board (E-IRB) Submission System FAQs

Human Subject Protection (HSP) Training FAQs
(includes information on HSP training for UK and non-UK study personnel on an IRB protocol

FDA-Regulated Research
 

UK Human Research Protection Program

What Needs Institutional Review Board (IRB) Review?

IRB Submission & Review Types

Scientific Design & Minimizing Risk

Conflict of Interest (COI)

Monitoring & Reporting Requirements

Qualifications, Training, & Oversight

Data & Safety Monitoring

Recruitment & Study Population

Informed Consent Process & Documentation

Complaints, Concerns, Suggestions, Questions or Requests for Information

Food & Drug Administration (FDA) Regulated Research

Community Engaged Research (CER)/Community Based Participatory Research (CBPR)

Outreach & Education for the Public and Potential Research Participants

Feasibility & Resources
 

Responsible Conduct of Research & Scholarly Activity (RCR) Training FAQs: Getting Started

• CITI RCR Course Information
• CITI Account
• CITI RCR Basic Course
• CITI RCR Refresher Course

Responsible Conduct of Research & Scholarly Activity (RCR) General FAQs

• University Mandate
• RCR Grants Requirements
• Collaborative Institutional Training Initiative (CITI)
• Other CITI Courses

UK Electronic Research Notebook (ERN) FAQs

• About LabArchives
• Creating Your Account
• Using LabArchives
• Inventory
• Miscellaneous

Research Misconduct FAQs