1|Page
C839 Knowledge Check Questions Only (Sample
Questions from Chapters 1 6)/ WGU C839
Introduction to Cryptography Practice Quiz
Which of these people would be classified as a vulnerable
subject?
A. Study coordinators studying for a CCRP exam
B. Employee under direct supervision of the PI
C. A 72 y/o woman
D. A 23 y/o man with chronic constipation -
...ANSWER...✓✓ B. Employee under direct supervision of
the PI
Which is one of the four components needed for a
consent process using a short form?
A. A witness must be present during the oral
presentation.
B. A legally authorized representative present (LAR).
C. A family member to act as the interpreter.
,2|Page
D. Exempt veterinary‐use‐only devices from IDE
regulations. - ...ANSWER...✓✓ A. A witness must be
present during the oral presentation.
What was the purpose of the Belmont Report?
A. Establish basic principles that physicians would abide
by.
B. Provide ethical principles developed by the World
Medical Association
C. Provide basic ethical principals and boundaries
between practice and research.
D. Exempt veterinary‐use‐only devices from IDE
regulations. - ...ANSWER...✓✓ C. Provide basic ethical
principals and boundaries between practice and research.
What is true of the Nuremberg Code?
A. Provide basic ethical principals and boundaries
between practice and research.
B. Provide ethical principals developed by the World
Medical Association
C. Exempt veterinary‐use‐only devices from IDE
, 3|Page
D. First set of principles outlining professional ethics for
clinical research - ...ANSWER...✓✓ D. First set of
principles outlining professional ethics for clinical
research
Which is a basic element of informed consent, under 21
CFR 50.25?
A. Disclosure of conflicts of interest
B. Description of foreseeable risks/discomforts
C. Consequences of early withdrawal
D. Statement about ClinicalTrials.gov - ...ANSWER...✓✓ B.
Description of foreseeable risks/discomforts
Who has the final authority to approve or reject a consent
form to be used in a clinical trial?
A. FDA
B. Sponsor
C. PI
D. IRB - ...ANSWER...✓✓ D. IRB
C839 Knowledge Check Questions Only (Sample
Questions from Chapters 1 6)/ WGU C839
Introduction to Cryptography Practice Quiz
Which of these people would be classified as a vulnerable
subject?
A. Study coordinators studying for a CCRP exam
B. Employee under direct supervision of the PI
C. A 72 y/o woman
D. A 23 y/o man with chronic constipation -
...ANSWER...✓✓ B. Employee under direct supervision of
the PI
Which is one of the four components needed for a
consent process using a short form?
A. A witness must be present during the oral
presentation.
B. A legally authorized representative present (LAR).
C. A family member to act as the interpreter.
,2|Page
D. Exempt veterinary‐use‐only devices from IDE
regulations. - ...ANSWER...✓✓ A. A witness must be
present during the oral presentation.
What was the purpose of the Belmont Report?
A. Establish basic principles that physicians would abide
by.
B. Provide ethical principles developed by the World
Medical Association
C. Provide basic ethical principals and boundaries
between practice and research.
D. Exempt veterinary‐use‐only devices from IDE
regulations. - ...ANSWER...✓✓ C. Provide basic ethical
principals and boundaries between practice and research.
What is true of the Nuremberg Code?
A. Provide basic ethical principals and boundaries
between practice and research.
B. Provide ethical principals developed by the World
Medical Association
C. Exempt veterinary‐use‐only devices from IDE
, 3|Page
D. First set of principles outlining professional ethics for
clinical research - ...ANSWER...✓✓ D. First set of
principles outlining professional ethics for clinical
research
Which is a basic element of informed consent, under 21
CFR 50.25?
A. Disclosure of conflicts of interest
B. Description of foreseeable risks/discomforts
C. Consequences of early withdrawal
D. Statement about ClinicalTrials.gov - ...ANSWER...✓✓ B.
Description of foreseeable risks/discomforts
Who has the final authority to approve or reject a consent
form to be used in a clinical trial?
A. FDA
B. Sponsor
C. PI
D. IRB - ...ANSWER...✓✓ D. IRB
