The principle investigator (PI) typically inactivates the study by providing a final status report to the Institutional Review Board (IRB).
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Q7: In healthcare research, studies that have significant
Q8: If informed consent cannot be documented (e.g.,
Q9: Any and all problems that occur during
Q10: Noncompliance is an action by the investigator,
Q11: It is the responsibility of the primary
Q13: An example of FDA-Regulated research would include
Q14: The Common Rule requires IRB approval of
Q15: The convened IRB (i.e., the full committee)
Q16: To highlight the need for IRB regulations
Q17: The Nazi Human Experiments lead to the
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