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No.Document TitleIDUpdatedHits
1 Does a pilot or feasibility study require IRB review and approval?
264312017-01-3037255
2 FAQs
223122020-01-0220231
3 Who may serve as a principal investigator on a protocol?
222212021-04-0819522
4 How do you change the responsible principal investigator (PI)?
252852017-02-0817929
5 What should I consider before conducting research with vulnerable populations?
222232016-12-2712866
6 Health Sciences IRBs Certificate of Confidentiality Guidance
228002019-11-1512589
7 Do I need to get consent for my exempt study?
550392020-09-169510
8 What things should I consider to protect subjects' privacy and confidentiality of data?
222992018-01-259303
9 Can changes of protocol be submitted for exemptions?
213542018-12-128841
10 How can I tell if my study is exempt, and what categories of exemption can I choose from?
213552019-02-138529
11 Does research with existing datasets require IRB review?
222282017-01-308323
12 I received an Action Letter/CAEPR or a revised IDB from the Sponsor. Does this need to be reported to the IRB?
217612017-01-097431
13 What are the criteria to be engaged in human subjects research at UW-Madison?
222062017-05-227137
14 Requirements for Registering with Clinicaltrials.gov
333032020-02-187002
15 Does my research with coded information or specimens require IRB review?
222262021-03-266940
16 I am a student researcher, what IRB approval do I need?
222222017-01-305904
17 What if my study team is not affiliated with a clinical department or unit but we need to recruit patients for our study?
268072018-07-205784
18 What documents related to IRB review should be maintained by the study team as part of the research record?
434832018-01-235684
19 I have a change of protocol and a continuing review coming up. Which should I submit first?
222552017-12-135589
20 I have samples/images/data that I want to use in a research study. When do I need IRB review?
216142020-02-055226

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