Results: 21-40 of 53
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No.Document TitleIDUpdatedHits
21 Health Sciences IRBs Certificate of Confidentiality Guidance
228002019-11-1512619
22 Should my industry sponsored research study be submitted to a commercial IRB?
410282019-10-183599
23 What are Material Transfer Agreements (MTAs) and when do I need one?
502652019-05-163583
24 What elements should I consider in my risk and benefit analysis?
223002019-02-283645
25 How can I tell if my study is exempt, and what categories of exemption can I choose from?
213552019-02-138553
26 What are exemption renewals?
539542018-12-123000
27 How does the 5-year expiration date affect my exemption?
270542018-12-125154
28 Can changes of protocol be submitted for exemptions?
213542018-12-128858
29 What if my study team is not affiliated with a clinical department or unit but we need to recruit patients for our study?
268072018-07-205803
30 Implementing the Campus Revised Continuing Review Policy
769102018-05-153158
31 When does something qualify as a Health Care Records Review Only application?
208712018-03-165197
32 What is IRBManager and why would I need to use it?
286872018-02-063050
33 What is an NCI CIRB study?
286862018-02-063898
34 What things should I consider to protect subjects' privacy and confidentiality of data?
222992018-01-259316
35 Do I need anything more than IRB approval for my NIH-funded study that involves large-scale genomic data analyses?
507822018-01-233779
36 What documents related to IRB review should be maintained by the study team as part of the research record?
434832018-01-235717
37 I have a change of protocol and a continuing review coming up. Which should I submit first?
222552017-12-135607
38 WIC Transition to SMART IRB
746892017-07-212702
39 My study involves working with students, parents, or staff at K-12 schools. Are there any special requirements that I need to be aware of related to my IRB submission?
741262017-07-123053
40 What are the criteria to be engaged in human subjects research at UW-Madison?
222062017-05-227170

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