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