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No.Document TitleIDUpdatedHits
1 Do the Safer Badgers building access requirements apply to research participants?
1085202021-01-2277
2 Remote Study Activities Guidance
1025802020-10-211475
3 How do I obtain informed consent remotely?
1013892020-10-211939
4 Do I need to get consent for my exempt study?
550392020-09-168177
5 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?
1025692020-07-01660
6 What is required from an IRB standpoint before restarting face-to-face research activities?
1025712020-07-011063
7 What are the first steps for study teams to get approval to restart face-to-face visits for an IRB-approved study?
1025702020-06-081011
8 What if I’m planning a new research study that requires face-to-face human subjects research activities?
1025732020-05-28552
9 Will remote study visits no longer be required after the campus begins allowing face-to-face visits to occur?
1025742020-05-28473
10 Are protocol and consent form changes required by the IRB for all studies prior to restarting face-to-face interactions?
1025722020-05-28561
11 What if my new COVID-19 study involves collecting and/or analyzing biospecimens?
997682020-05-13845
12 Does my research with coded information or specimens require IRB review?
222262020-04-166282
13 What if researchers have an Initial Review application for a non-COVID-19 study currently under review?
993302020-04-14773
14 Obtaining Informed Consent from COVID-19 Positive Patients
999642020-04-021017
15 Updating Name and Contact Information in ARROW
686212020-03-112618
16 Personnel Update FAQ
982462020-02-26777
17 Requirements for Registering with Clinicaltrials.gov
333032020-02-186279
18 I have samples/images/data that I want to use in a research study. When do I need IRB review?
216142020-02-054679
19 FAQs
223122020-01-0218971
20 Health Sciences IRBs Certificate of Confidentiality Guidance
228002019-11-1511767

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