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No.Document TitleIDUpdatedHits
1 Should my industry sponsored research study be submitted to a commercial IRB?
410282018-01-171440
2 How to Remove Study Team Members
760022017-12-14341
3 FAQs
223122017-12-1313266
4 I have a change of protocol and a continuing review coming up. Which should I submit first?
222552017-12-133268
5 Implementing the Campus Revised Continuing Review Policy
769102017-09-26248
6 Requirements for Registering with Clinicaltrials.gov
333032017-09-183358
7 What if my study team is not affiliated with a clinical department or unit but we need to recruit patients for our study?
268072017-08-212820
8 WIC Transition to SMART IRB
746892017-07-21320
9 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?
741262017-07-12299
10 What are the criteria to be engaged in human subjects research at UW-Madison?
222062017-05-223991
11 What is IRBManager and why would I need to use it?
286872017-05-191532
12 Who can I contact if I have concerns about human research protections at UW-Madison?
223042017-05-182316
13 What is an NCI CIRB study?
286862017-02-132115
14 Why is the NCI CIRB emailing me?
286882017-02-131366
15 How do you change the responsible principal investigator (PI)?
252852017-02-0811982
16 Does research with existing datasets require IRB review?
222282017-01-304351
17 Does a pilot or feasibility study require IRB review and approval?
264312017-01-3018667
18 How can I tell if my study is exempt, and what categories of exemption can I choose from?
213552017-01-304900
19 When does something qualify as a Non-Exempt Medical Records review?
208712017-01-303181
20 I am a student researcher, what IRB approval do I need?
222222017-01-303607

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