Results: 21-40 of 53
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No.Document TitleIDUpdatedHits
21 Implementing the Campus Revised Continuing Review Policy
769102018-05-153503
22 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?
741262017-07-123422
23 Obtaining Informed Consent from COVID-19 Positive Patients
999642020-04-022231
24 Personnel Update FAQ
982462020-02-261768
25 Remote Study Activities Guidance
1025802020-10-212557
26 Requirements for Registering with Clinicaltrials.gov
333032020-02-187390
27 Should my industry sponsored research study be submitted to a commercial IRB?
410282019-10-183866
28 Updating Name and Contact Information in ARROW
686212020-03-113516
29 What are exemption renewals?
539542018-12-123332
30 What are Material Transfer Agreements (MTAs) and when do I need one?
502652019-05-163897
31 What are the criteria to be engaged in human subjects research at UW-Madison?
222062017-05-227645
32 What are the first steps for study teams to get approval to restart face-to-face visits for an IRB-approved study?
1025702020-06-081804
33 What documents related to IRB review should be maintained by the study team as part of the research record?
434832018-01-236570
34 What elements should I consider in my risk and benefit analysis?
223002019-02-284132
35 What if I’m planning a new research study that requires face-to-face human subjects research activities?
1025732020-05-281306
36 What if my new COVID-19 study involves collecting and/or analyzing biospecimens?
997682020-05-131556
37 What if my research involves the use of fetal tissue?
222292017-01-034833
38 What if my study team is not affiliated with a clinical department or unit but we need to recruit patients for our study?
268072018-07-206244
39 What if researchers have an Initial Review application for a non-COVID-19 study currently under review?
993302020-04-141526
40 What if samples/images/data are coming from an outside source?
216172017-01-054813

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