{"id":117494,"date":"2023-08-28T21:32:30","date_gmt":"2023-08-28T21:32:30","guid":{"rendered":"https:\/\/learnexams.com\/blog\/?p=117494"},"modified":"2023-08-28T21:32:33","modified_gmt":"2023-08-28T21:32:33","slug":"citi-exams-questions-and-answers-latest-update-solution-pack","status":"publish","type":"post","link":"https:\/\/www.learnexams.com\/blog\/2023\/08\/28\/citi-exams-questions-and-answers-latest-update-solution-pack\/","title":{"rendered":"CITI Exams Questions And Answers Latest Update Solution Pack"},"content":{"rendered":"\n

Citi Exams Questions And Answers
Which of the following is included in the Nuremberg Code: – voluntary consent
The National Research Act of 1974 – Established the National Commission.
Informed consent is considered an application of which Belmont principle? – Respect for
Persons
Issued in 1974, 45 CFR 46 raised to regulatory status: – US Public Health Service Policy
Which of the following brought increased public attention to the problems with the IRB
system? – Death of Jesse Gelsinger
The use of prisoners in research is a concern under the Belmont principle of Justice
because: – Prisoners may be used to conduct research that only benefits the larger society
Which of the following was the result of the Beecher article? – 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? – 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.
How long is an investigator required to keep consent documents, IRB correspondence, and
research records? – For a minimum of three years after completion of the study
According to federal regulations, which of the following best describes when expedited
review of a new, proposed study may be used by the IRB? – The study involves no more
than minimal risk and meets one of the allowable categories of expedited review specified
in federal regulations
Amendments involving changes to IRB approved protocols do NOT need prior IRB approval
if: – The changes must be immediately implemented for the health and well being of the
subject.
IRB continuing review of an approved protocol must: – Occur at least annually.
An investigator is confronted with a life-threatening situation that necessitates using a test
article in a human subject who is unable to provide informed consent and there is no time
to obtain consent from the individual’s legal representative and no alternative method or
recognized therapy is available. Under the FDA regulations for using test articles, which of
the following describes the best course of action for the investigator: – The investigator and<\/p>\n\n\n\n

CITI Training Human Subjects Protection
Basic Course
persons with diminished autonomy are entitled to protection – The Belmont Report’s
principle of respect for persons incorporates at least two ethical convictions: first, that
individuals should be treated as autonomous agents, and second, that:
Determining that the study has a maximization of benefits and a minimization of risks. –
Which of the following is an example of how the principle of beneficence can be applied to a
study employing human subjects?
Respect for Persons, Beneficence, Justice – Which of the following are the three principles
discussed in the Belmont Report?
The Public Health Service Tuskegee Study of Untreated Syphilis in the Negro Male. – Which
of the following studies is linked most directly to the establishment of the National
Research Act in 1974 and ultimately to the Belmont Report and Federal regulations for
human subject protection?
Respect for persons. – Humphreys collecting data for the Tearoom Trade study under the
pretense that he was a lookout is an example of a violation of the principle of:
Harvard “Tastes, Ties, and Time (T3)” study (2006-2009)” study – The researcher’s failure
to protect research subjects from deductive disclosure is the primary ethical violation in
which of the following studies?
Justice – According to the Belmont Report, the moral requirement that there be fair
outcomes in the selection of research subjects, expresses the principle of:
Potential benefits justify the risks of harm. – The Belmont principle of beneficence requires
that:<\/p>\n\n\n\n