If informed consent cannot be documented (e.g., telephone surveys), the researcher may request a waiver of documentation of informed consent, which must be approved by the IRB.
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Verified
Q3: The Belmont Princple led to the development
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
Q9: Any and all problems that occur during
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
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