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No.Document TitleIDUpdatedHits
1 FAQs
223122017-09-2812858
2 Implementing the Campus Revised Continuing Review Policy
769102017-09-26146
3 Requirements for Registering with Clinicaltrials.gov
333032017-09-183242
4 I have a change of protocol and a continuing review coming up. Which should I submit first?
222552017-09-073185
5 How to Remove Study Team Members
760022017-08-24209
6 What if my study team is not affiliated with a clinical department or unit but we need to recruit patients for our study?
268072017-08-212729
7 WIC Transition to SMART IRB
746892017-07-21224
8 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?
741262017-07-12234
9 What are the criteria to be engaged in human subjects research at UW-Madison?
222062017-05-223897
10 What is IRBManager and why would I need to use it?
286872017-05-191477
11 Who can I contact if I have concerns about human research protections at UW-Madison?
223042017-05-182260
12 How do I find a submission in ARROW and check its status?
199752017-05-102340
13 Where do I go to create a new change, personnel change, continuing review, or reportable event in ARROW?
199712017-03-224230
14 What is an NCI CIRB study?
286862017-02-132042
15 Why is the NCI CIRB emailing me?
286882017-02-131316
16 How do you change the responsible principal investigator (PI)?
252852017-02-0811866
17 Does research with existing datasets require IRB review?
222282017-01-304244
18 Does a pilot or feasibility study require IRB review and approval?
264312017-01-3017505
19 How can I tell if my study is exempt, and what categories of exemption can I choose from?
213552017-01-304794
20 When does something qualify as a Non-Exempt Medical Records review?
208712017-01-303106

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