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No.Document TitleIDUpdatedHits
1 Are protocol and consent form changes required by the IRB for all studies prior to restarting face-to-face interactions?
1025722020-05-28996
2 Can changes of protocol be submitted for exemptions?
213542018-12-128858
3 Do I need anything more than IRB approval for my NIH-funded study that involves large-scale genomic data analyses?
507822018-01-233779
4 Do I need to get consent for my exempt study?
550392020-09-169532
5 Do the Safer Badgers building access requirements apply to research participants?
1085202021-01-22576
6 Does a pilot or feasibility study require IRB review and approval?
264312017-01-3037295
7 Does my research with coded information or specimens require IRB review?
222262021-03-266958
8 Does research with existing datasets require IRB review?
222282017-01-308348
9 Does the IRB require submission and review of Manuals for Procedures
268082016-12-195038
10 FAQs
223122020-01-0220254
11 Health Sciences IRBs Certificate of Confidentiality Guidance
228002019-11-1512619
12 How can I tell if my study is exempt, and what categories of exemption can I choose from?
213552019-02-138553
13 How do I obtain informed consent remotely?
1013892020-10-213506
14 How do you change the responsible principal investigator (PI)?
252852017-02-0817945
15 How does the 5-year expiration date affect my exemption?
270542018-12-125154
16 How should investigators handle subject complaints?
384172016-12-223389
17 I am a student researcher, what IRB approval do I need?
222222017-01-305919
18 I have a change of protocol and a continuing review coming up. Which should I submit first?
222552017-12-135606
19 I have samples/images/data that I want to use in a research study. When do I need IRB review?
216142020-02-055235
20 I received an Action Letter/CAEPR or a revised IDB from the Sponsor. Does this need to be reported to the IRB?
217612017-01-097447

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