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