1. Eloqua - Email settings when using Design Editor
  2. Completing the Subject Identification and Recruitment Section
  3. INTER-LS (Interdisciplinary Courses-L&S) Subject Listing
  4. Office 365 - Default subject naming behavior when inviting a resource calendar
  5. Guidance on Making Editorial Changes to Subject-Facing Study Materials
  6. How should investigators handle subject complaints?
  7. Subject Recruitment and Screening Procedures Guidance Index
  8. Subject Population
  9. Subject Recruitment: Continued
  10. Subject Population: Vulnerable Group Checklist
  11. Article: "You Don't Know Me, But...": Access to Patient Data and Subject Recruitment in Human Subjects Research
  12. Additional Requirements When Conducting Human Subjects Research with Department of Defense (DOD) Support
  13. Course Search & Enroll - Searching for Classes
  14. Issues in Human Subjects Research When State Law May Apply
  15. Documenting Consent Electronically or for Remote Subjects Guidance
  16. Re-Consenting Subjects Guidance
  17. SIS/Getting Started - Codes in SIS: Terms, Sessions and Subjects
  18. Guidance on Exemption: Not Human Subjects Research
  19. Changes to Human Subjects Regulations and Policies
  20. Changes to Eliminate Immediate Hazards to Subjects Guidance
  21. UW-Madison College-Level Examination Program (CLEP)
  22. Additional Requirements When Conducting Human Subjects Research with Department of Justice (DOJ) Support
  23. Upcoming Changes to Human Subjects Regulations and Policies
  24. Guidance Regarding Types of Supporting Materials that Require IRB Review and Approval
  25. SIS/Building Your Schedule of Classes - Creating a Topics Course
  26. Conflict of Interest Policy
  27. UW-Madison Custodian Fund Advances
  28. Brief Summary of Investigator Responsibilities Related to the Protection of Human Subjects for Exempt Research
  29. KB User's Guide - Home Tab - My Profile
  30. UW-Madison Cross-Listed and "Meets With" Course Information
  31. Additional Requirements When Conducting Human Subjects Research with Department of Education (ED) Support
  32. What things should I consider to protect subjects' privacy and confidentiality of data?
  33. Recruitment of Subjects with Status Relationship with the Research Team
  34. What are the criteria to be engaged in human subjects research at UW-Madison?
  35. HS-IRBs News June 2013
  36. SIS - Default Settings for Using SIS
  37. UW Digital ID (Personal Certificate) - Secondary Email Addresses
  38. Office 365 - Approve ClickDimensions to Send DMARC-Compliant Email from My Domain
  39. Office 365 - Approve Campaign Monitor to Send DMARC-Compliant Email from My Domain
  40. Office 365 - Approve iContact to Send DMARC-Compliant Email from My Domain
  41. Office 365 - Approve SendGrid to Send DMARC-Compliant Email from My Domain
  42. Office 365 - Approve Constant Contact to Send DMARC-Compliant Email from My Domain
  43. Office 365 - Approve Emma to Send DMARC-Compliant Email from My Domain
  44. Office 365 - Approve MailChimp to Send DMARC-Compliant Email from My Domain
  45. Office 365 - DMARC Compliance for Amazon Simple Email Service
  46. KB User's Guide - Users Tab - Adding a User
  47. SIS - Academic Structure at UW-Madison
  48. Eloqua - Email settings when using HTML Editor
  49. Office 365 - DMARC Info tool
  50. Office 365 - Steps to make UW-Madison email DMARC compliant
  51. Office 365 - Publishing a Custom DMARC Record for Your Email Domain in DNS
  52. COVID-19 Updates
  53. Review of FDA-Regulated Research Policy
  54. How do I modify my study so study visits can occur remotely?
  55. Can I still interact with my study subjects?
  56. What if I decide to temporarily halt study visits?
  57. What about effects on enrollment goals?
  58. What software platforms can I use to conduct remote visits or procedures?
  59. Training & Education
  60. Additional Requirements When Conducting Human Subjects Research with Environmental Protection Agency (EPA) Support
  61. Human Participants Research
  62. Post Approval Monitoring Program Services
  63. IRB Workshops & Outreach
  64. Clinical/Translational Research Proposal
  65. Bio-ARROW - SmartForm - Recombinant Synthetic DNA/RNA Materials
  66. HRPP Guidance, Forms and Resources
  67. Research Policy, Compliance, and Safety Training Courses
  68. Instructions for Completing CITI Refresher Training
  69. Who may serve as a principal investigator on a protocol?
  70. VA Research: Policy for IRB Review of Human Subjects Research that Falls Under VA Purview
  71. Human Subjects Research Protection Program (HRPP) Policy Index
  72. Unanticipated Problems
  73. IRB Review of Study Resources
  74. Reporting to Institutional and External Authorities
  75. Accessing ARROW for Administrative Personnel at UW-Madison Not Engaged in Human Subjects Research
  76. What if I’m planning a new research study that requires face-to-face human subjects research activities?
  77. Human Research Protection Program Newsletter
  78. Research
  79. Do all human subjects regulations apply as usual during this pandemic?
  80. Informed Consent: Illiterate Subjects
  81. Case Reports and Case Series Guidance
  82. Additional Requirements When Conducting Human Subjects Research with Department of Energy (DOE) Support
  83. Frequently Asked Questions about Collaborative Research Requirements
  84. Guidance Regarding Self-Experimentation of Researchers as Study Subjects
  85. How does the 5-year expiration date affect my exemption?
  86. Instructions for Completing CITI Human Participants Research Training
  87. De-Identified Publicly Available Datasets Guidance
  88. OHRP Guidance on Engagement of Institutions in Human Subjects Research
  89. List of Approved De-Identified Publicly Available Datasets
  90. Devices Implanted or Applied to Subjects Guidance
  91. Certify Not Human Subjects Research [Glossary item]
  92. HS-IRBs News July 2013
  93. HS-IRBs News February 2013
  94. HS-IRBs News May 2012
  95. HS-IRBs News March 2012