Adults Lacking Capacity to Consent 
Appealing IRB Decisions
Assent of Children and Parental Permission
Assuring Research Involving Test Articles (Drugs, Biologics, Nutritional Supplements or Devices) Complies with FDA Requirements 
Case Reports
Changes/Amendments to Approved Research
Clinician/Investigator-Held IDEs
Compensation for Identifying and Enrolling Subjects
Continuing Review
Convened IRB Meetings: Preparation, Conduct and Follow-up
Criteria for IRB Approval
Data and Safety Monitoring Plans
Deferring Review of Marshfield Clinic Studies to an External IRB
Determining Engagement in Research
Determining Which Projects Require Review More Often than Annually
Employees, Staff and Students as Research Subjects
Ending IRB Oversight
Enhancing Understanding and Responding to Human Research Questions, Concern & Input
Exempt Projects, Review of
Expanded Access to Investigational Drugs, Biologics or Devices
Expedited Review
Guests at IRB Meetings
Guidance on Returning Research Results to Subjects
Guidance on the Approvability of HIPAA Authorization Waivers and Alterations
Human Participants in Research & the Human Participation Protection Program
Human Subject Protection Training
Humanitarian Use Devices
Identification, Recruitment and Compensation of Research Participants
Informed Consent for Research
Informed Consent of Illiterate or Legally Blind Research Subjects
Informed Consent of Non-English Speaking Subjects
International Conference on Harmonisation (ICH) Good Clinical Practice (GCP) Guidelines and IRB Review
IRB Approvals with Conditions
IRB Chair, IRB Member and IRB Staff Evaluation Process
IRB Consideration of Conflict of Interest: Member, Guest Reviewer and Investigator
IRB Membership
IRB Review of Databases, Registries, and Bio-Banks
IRB Review of Protocols in Long Term Follow Up (LTFU)
IRB Review of Transnational Research
Marshfield Clinic Research Foundation IRB (MCRF IRB) as IRB of Record
MCRF Investigators and Multi-Site Research
Phase IV Drug Studies, IRB Review
Prisoners In Research
Program Evaluation (including Quality Assurance and Quality Improvement): Determining the Need for IRB Review
Projects Needing Verification from Sources other than the Investigator
Public Health Research vs. Non-Research
Record Keeping and Retention
Reporting IRB Actions and Findings to the Investigator and Institution
Reporting of New Findings to the IRB
Reporting to IRB, Institutional Officials, and Regulatory Bodies
Research Data Protection
Review of Investigational Device Research
Scientific or Scholarly Validity Review Requirements
Signatory Authority
Suspension and Termination of Research
Unanticipated Problems, Reporting and Review of
Vulnerable Populations
Withdrawal of Subjects from Research