Citi exam questions with 100% correct
answers4
Which of the following is included in the Nuremberg Code: - ANSWERS-voluntary consent
The National Research Act of 1974 - ANSWERS-Established the National Commission.
Informed consent is considered an application of which Belmont principle? - ANSWERS-Respect
for Persons
Issued in 1974, 45 CFR 46 raised to regulatory status: - ANSWERS-US Public Health Service Policy
Which of the following brought increased public attention to the problems with the IRB system?
- ANSWERS-Death of Jesse Gelsinger
The use of prisoners in research is a concern under the Belmont principle of Justice because: -
ANSWERS-Prisoners may be used to conduct research that only benefits the larger society
Which of the following was the result of the Beecher article? - ANSWERS-Realization that ethical
abuses are not limited to the Nazi regime
A subject in a clinical research trial experiences a serious, unanticipated adverse drug
experience. How should the investigator proceed, with respect to the IRB, after the discovery of
the adverse event occurrence? - ANSWERS-Report the adverse drug experience in a timely
manner, in keeping with the IRB's policies and procedures, using the forms or the mechanism
provided by the IRB.
answers4
Which of the following is included in the Nuremberg Code: - ANSWERS-voluntary consent
The National Research Act of 1974 - ANSWERS-Established the National Commission.
Informed consent is considered an application of which Belmont principle? - ANSWERS-Respect
for Persons
Issued in 1974, 45 CFR 46 raised to regulatory status: - ANSWERS-US Public Health Service Policy
Which of the following brought increased public attention to the problems with the IRB system?
- ANSWERS-Death of Jesse Gelsinger
The use of prisoners in research is a concern under the Belmont principle of Justice because: -
ANSWERS-Prisoners may be used to conduct research that only benefits the larger society
Which of the following was the result of the Beecher article? - ANSWERS-Realization that ethical
abuses are not limited to the Nazi regime
A subject in a clinical research trial experiences a serious, unanticipated adverse drug
experience. How should the investigator proceed, with respect to the IRB, after the discovery of
the adverse event occurrence? - ANSWERS-Report the adverse drug experience in a timely
manner, in keeping with the IRB's policies and procedures, using the forms or the mechanism
provided by the IRB.
