Any and all problems that occur during the study, must be immediately reported to the IRB committee.
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Q4: A study that tested the efficiacy of
Q5: For a study to be categorized as
Q6: A study that uses medical chart reviews
Q7: In healthcare research, studies that have significant
Q8: If informed consent cannot be documented (e.g.,
Q10: Noncompliance is an action by the investigator,
Q11: It is the responsibility of the primary
Q12: The principle investigator (PI) typically inactivates the
Q13: An example of FDA-Regulated research would include
Q14: The Common Rule requires IRB approval of
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