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No.Document TitleIDUpdatedHits
1 Who may serve as a principal investigator on a protocol?
222212021-04-0820005
2 Does my research with coded information or specimens require IRB review?
222262021-03-267439
3 Do the Safer Badgers building access requirements apply to research participants?
1085202021-01-22942
4 Remote Study Activities Guidance
1025802020-10-212572
5 How do I obtain informed consent remotely?
1013892020-10-214476
6 Do I need to get consent for my exempt study?
550392020-09-1610409
7 What role can the IRB play for department chairs, center directors, and deans who are determining whether specific research studies can reopen face-to-face visits?
1025692020-07-011438
8 What is required from an IRB standpoint before restarting face-to-face research activities?
1025712020-07-011911
9 What are the first steps for study teams to get approval to restart face-to-face visits for an IRB-approved study?
1025702020-06-081820
10 What if I’m planning a new research study that requires face-to-face human subjects research activities?
1025732020-05-281315
11 Will remote study visits no longer be required after the campus begins allowing face-to-face visits to occur?
1025742020-05-281241
12 Are protocol and consent form changes required by the IRB for all studies prior to restarting face-to-face interactions?
1025722020-05-281311
13 What if my new COVID-19 study involves collecting and/or analyzing biospecimens?
997682020-05-131579
14 What if researchers have an Initial Review application for a non-COVID-19 study currently under review?
993302020-04-141542
15 Obtaining Informed Consent from COVID-19 Positive Patients
999642020-04-022243
16 Updating Name and Contact Information in ARROW
686212020-03-113529
17 Personnel Update FAQ
982462020-02-261778
18 Requirements for Registering with Clinicaltrials.gov
333032020-02-187407
19 I have samples/images/data that I want to use in a research study. When do I need IRB review?
216142020-02-055774
20 FAQs
223122020-01-0220902

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