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Module 4 Objectives Continuing Review Unanticipated Developments Adverse Events Consent Document Revisions Quiz |
Quiz
Check your knowledge of the after approval requirements. Click on the correct answer to each question.
When you are finished, the Next button will take you to Test Your Understanding, or the Menu button will take you to the menu screen.
Question 1 of 5
Once a project has been initially reviewed and approved by the IRB, no further review is necessary.
The death of a study subject should be reported to the IRB if it is believed to be unrelated to the study.
Unexpected problems whose nature, severity, or frequency are not described in the information provided to the IRB or to participants are called:
adverse events
bad luck
side effects
mistakes
Question 4 of 5
Continuing review of a study by the IRB occurs at least:
weekly
monthly
annually
biannually
Question 5 of 5
The terms of a continuing review are outlined when original approval is granted.
