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No.Document TitleIDUpdatedHits
1 What if my study team is not affiliated with a clinical department or unit but we need to recruit patients for our study?
268072018-07-203231
2 Implementing the Campus Revised Continuing Review Policy
769102018-05-15695
3 FAQs
223122018-04-0414572
4 Can changes of protocol be submitted for exemptions?
213542018-04-036002
5 When does something qualify as a Health Care Records Review Only application?
208712018-03-163496
6 How to Remove Study Team Members
760022018-03-14830
7 What is IRBManager and why would I need to use it?
286872018-02-061762
8 What is an NCI CIRB study?
286862018-02-062395
9 Do I need to get consent for my exempt study?
550392018-01-253012
10 What are the Human Subjects Research training (and other training) requirements?
225952018-01-2517333
11 What things should I consider to protect subjects' privacy and confidentiality of data?
222992018-01-255246
12 What are exemption renewals?
539542018-01-231130
13 Do I need anything more than IRB approval for my NIH-funded study that involves large-scale genomic data analyses?
507822018-01-231706
14 What are Material Transfer Agreements (MTAs) and when do I need one?
502652018-01-231578
15 How does the 5-year expiration date affect my exemption?
270542018-01-232888
16 What documents related to IRB review should be maintained by the study team as part of the research record?
434832018-01-232124
17 Should my industry sponsored research study be submitted to a commercial IRB?
410282018-01-231710
18 I have a change of protocol and a continuing review coming up. Which should I submit first?
222552017-12-133587
19 Requirements for Registering with Clinicaltrials.gov
333032017-09-183778
20 WIC Transition to SMART IRB
746892017-07-21652

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