- Article: A Broken Contract
- Article: A Comprehensive Analysis of MRI Research Risks: In Support of Full Disclosure
- Article: Apple's New ResearchKit: 'Ethics Quagmire' or Medical Research Aid?
- Article: As Data Overflows Online, Researchers Grapple With Ethics
- Article: Balancing Risks and Benefits in Clinical Trials
- Article: Blood Samples Raise Questions of Privacy
- Article: Clinical Trials, Wrapped in Red Tape
- Article: Disclosure of Financial Relationships to Participants in Clinical Research
- Article: For Henrietta Lacks' Famous Cells, New and Unique Protection
- Article: How Variability in the Institutional Review Board Review Process Affects Minimal-Risk Multisite Health Services Research
- Article: Lessons from researcher rehab
- Article: Pediatric Magnetic Resonance Research and the Minimal-Risk Standard
- Article: Rx Risks Not Dislosed to Trial Participants
- Article: The Importance of Purpose: Moving Beyond Consent in the Societal Use of Personal Health Information
- Article: Updating Research Oversight for the 21st Century
- Belmont Report
- Brief Overview of Regulatory Basis of IRB Authority and Review Responsibilities
- Brief Responsibilities of an HS-IRB Member
- Brief Responsibilities of an MR-IRB Member
- Cheat Sheet (w/ screenshots) for Initial Reviews in ARROW
- Children as research participants: Regulations
- Continuing Review & Changes of Protocol
- Criteria for IRB Approval: 45 CFR 46.111 (DHHS), 21 CFR 56.111 (FDA), and 38 CFR 16.111 (VA)
- Drugs, Biologics, and Devices: Regulations
- Finding Study-Related Documents in ARROW
- For IRB Members
- Genetic Testing or Analysis
- Guidance for UW Madison Health Sciences IRB & Minimal Risk IRB Primary Reviewers for Summarizing Initial Review Applications
- How to Conduct a Deferral Response Review in ARROW
- How to Conduct a Modification Response Review in ARROW
- How to Conduct PRS Review
- IEP IRB Member FAQ
- Informed Consent Process, Elements, and Waivers
- Initial Review Tips for IRB Members
- IRB Member FAQs
- IRB Member Newsletter -- Volume 12 (Summer 2019)
- IRB Member Newsletter--Scheduling Special Edition
- IRB Member Newsletter--Volume 1 (Fall 2009)
- IRB Member Newsletter--Volume 10 (Fall 2017)
- IRB Member Newsletter--Volume 11 (Spring 2018)
- IRB Member Newsletter--Volume 2 (Winter 2010)
- IRB Member Newsletter--Volume 3 (Summer 2011)
- IRB Member Newsletter--Volume 4 (Winter 2011/2012)
- IRB Member Newsletter--Volume 5 (Spring/Summer 2012)
- IRB Member Newsletter--Volume 6 (Fall 2012)
- IRB Member Newsletter--Volume 7 (Spring 2013)
- IRB Member Newsletter--Volume 8 (Winter 2013)
- IRB Member Newsletter--Volume 9 (Summer 2015)
- IRB Member Workspace Navigation Guide for IRB Members
- Making a Motion at IRB Meetings
- Meeting Workspace Navigation Guide for IRB Members
- New IRB Members Guide
- Noncompliance, Protocol Exceptions and Deviations
- Overview of the Accreditation Process and UW-Madison's Human Research Protections Program
- Pregnant Women, Fetuses and Neonates: Regulations
- Primary Reviewer Guidance for Initial Reviews
- Prisoners: Regulations
- Privacy & Confidentiality
- Review Processes Other Than Full-Board
- Reviewing Initial Applications In ARROW
- Reviewing IRB Meeting Minutes in ARROW
- Scientist Screwed Up? Send 'em to Researcher Rehab (2017)
- Study Personnel Financial Conflicts of Interest and HS IRBs Review Guidance
- The Nuremberg Code 70 Years Later (2017)
- Unanticipated Problems and Serious Adverse Events