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