| Will you accept my CITI training from my previous institution? |
Training for Researchers and Research Team, I'm a new researcher... |
| Will you accept a different CITI module if it is not expired? |
Training for Researchers and Research Team |
| Will I be paid for participating in research? |
Participating in Research |
| Why won't my application submit? |
IRBOnline - Electronic Submission System |
| Why doesn't my study have an expiration date? |
Continuing Reviews, Annual HRPP Progress Updates |
| Why do problems/events need to be reported? |
Unanticipated Problems |
| Who is responsible for completing the application to transition to IRBOnline? |
IRBOnline - Electronic Submission System, Transitioning Old Projects to IRBOnline |
| Who can submit a Non Human Subject Research application? |
IRBOnline - Electronic Submission System, Non-Human Subject Research, Does my study need IRB approval? |
| Who can participate in research? |
Participating in Research |
| Who can build a Data or Biospecimen Repository? |
Building Data or Biospecimen Repositories for Future Use |
| Who can be a Principal Investigator (PI)? |
PI Responsibilities, IRBOnline - Electronic Submission System |
| Where is the Research Equipment Form? |
Forms |
| Where do I list the research team on a Non Human Subject Research form? |
IRBOnline - Electronic Submission System, Non-Human Subject Research |
| What qualifies as DoD research? |
Department of Defense Research |
| What is the timeline for transitioning a project to IRBOnline? |
Transitioning Old Projects to IRBOnline, IRBOnline - Electronic Submission System |
| What is the timeframe requirement for transition? |
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| What is the IRB Review Process for Transitioned Projects? |
Transitioning Old Projects to IRBOnline, IRBOnline - Electronic Submission System |
| What is the difference between consent and assent? |
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| What is meant by Active Projects in IRBOnline? |
Transitioning Old Projects to IRBOnline, IRBOnline - Electronic Submission System |
| What is ClinicalTrials.gov and do I have to do it? |
Clinical Trials |
| What does the IRB do with Report Forms after they are submitted? |
Report Forms |
| What are the possible consequences for deviating? |
Deviations |
| What are the DoD components? |
Department of Defense Research |
| What are the consequences for submitting possible non-compliance late? |
Deviations, Report Forms |
| What are the consequences for submitting a possible Unanticipated Problem late? |
Unanticipated Problems, Report Forms, Breaches of Confidentiality |
| Should I submit an Amendment or a Report Form? |
Report Forms, Amendments |
| Should I submit an Amendment or a New Study? |
Amendments |
| Once my project is determined exempt, do I need to do anything else with the application? |
Exempt Research, Final Project Reports, Report Forms, Unanticipated Problems, Deviations |
| My research will be done in another country. Do I have to obtain IRB review and approval from the University of Illinois IRB? |
International Research |
| Is IRB Approval Necessary to Build a Registry? |
Building Data or Biospecimen Repositories for Future Use |