Results : 1-20 of 96
Search result for "subject": 1-20
No.Document TitleIDSiteUpdatedHits
1 Bio-ARROW - SmartForm - Recombinant Synthetic DNA/RNA Materials
43075ARROW - Institutional Biosafety Committee2022-11-035990
2 Clinical/Translational Research Proposal
65754Dermatology2022-04-042939
3 Informed Consent: Illiterate Subjects
21458ED/SBS IRB - ARROW Help2019-11-271388
4 IRB Workshops & Outreach
86940ED/SBS IRB Office2022-04-115902
5 Changes to Human Subjects Regulations and Policies
77658ED/SBS IRB Office2019-01-253791
6 **** Eloqua - Email settings when using Design Editor
104732Eloqua Marketing Automation2022-08-052613
7 Eloqua - Email settings when using HTML Editor
107720Eloqua Marketing Automation2022-08-051616
8 How should investigators handle subject complaints?
38417Health Sciences Institutional Review Boards2016-12-223944
9 Documenting Consent Electronically or for Remote Subjects Guidance
76726Health Sciences Institutional Review Boards2022-11-3053813
10 How does the 5-year expiration date affect my exemption?
27054Health Sciences Institutional Review Boards2018-12-125778
11 Subject Recruitment and Screening Procedures Guidance Index
18624Health Sciences Institutional Review Boards2020-03-0527367
12 HS-IRBs News May 2012
24399Health Sciences Institutional Review Boards2015-06-094820
13 What if I’m planning a new research study that requires face-to-face human subjects research activities?
102573Health Sciences Institutional Review Boards2020-05-281565
14 What are the criteria to be engaged in human subjects research at UW-Madison?
22206Health Sciences Institutional Review Boards2017-05-227925
15 Upcoming Changes to Human Subjects Regulations and Policies
77150Health Sciences Institutional Review Boards2019-01-238024
16 Training & Education
18334Health Sciences Institutional Review Boards2020-03-1839289
17 Certify Not Human Subjects Research [Glossary item]
17521Health Sciences Institutional Review Boards2015-10-134449
18 How do I modify my study so study visits can occur remotely?
98903Health Sciences Institutional Review Boards2020-07-082067
19 Guidance Regarding Types of Supporting Materials that Require IRB Review and Approval
27488Health Sciences Institutional Review Boards2017-10-0243207
20 Brief Summary of Investigator Responsibilities Related to the Protection of Human Subjects for Exempt Research
78821Health Sciences Institutional Review Boards2019-01-244156
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