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No.Document TitleIDUpdatedHits
21 What if my new COVID-19 study involves collecting and/or analyzing biospecimens?
997682020-05-131639
22 Can I still interact with my study subjects?
989002020-04-142823
23 What if researchers have an Initial Review application for a non-COVID-19 study currently under review?
993302020-04-141605
24 What is the process for single patient emergency use and expanded access protocols?
989072020-04-071529
25 Obtaining Informed Consent from COVID-19 Positive Patients
999642020-04-022326
26 Should I submit a New Information report or a Change of Protocol for my COVID-19-related protocol updates?
994562020-03-251396
27 What information should I include in my COVID-19-related change of protocol?
994552020-03-251540
28 What if I decide to temporarily halt study visits?
989022020-03-251722
29 Do all human subjects regulations apply as usual during this pandemic?
988972020-03-251500
30 What about effects on enrollment goals?
989062020-03-251374
31 What software platforms can I use to conduct remote visits or procedures?
991162020-03-191575
32 What about studies for which the UW is serving as the reviewing IRB?
990302020-03-171325
33 What about studies reviewed by a non-UW-Madison IRB?
990312020-03-171459
34 Do I need to revise my consent documents to reflect the risks of COVID-19 if in-person study interaction will still occur?
989052020-03-161413
35 What about study enrollment?
989012020-03-161562
36 Are the IRBs prioritizing reviews of submissions?
988962020-03-161669
37 HS IRBs News January 2020
972222020-02-272192
38 Health Sciences IRBs Newsletter - Archive
183972020-01-215936
39 HS IRBs News December 2019
966242020-01-212049
40 HS IRBs News November 2019
959762019-12-191798

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