CITI Training - Good Clinical Practice Exam | Verified Exam Questions and Answers | Latest Updated Study Material 2026

CITI Training - Good Clinical Practice Exam | Verified Exam Questions
and Answers | Latest Updated Study Material 2026

Question:

CITI Training - Good Clinical Practice Exam |Comprehensive
Good Clinical Practice Course for Clinical Trials with Investigational Drugs and Medical
Devices
Answer:


Question:

Which of the following are the three principles included in the Belmont Report?
Answer:

Respect for Persons, Beneficence, Justice.

Question:

Which of the following is an example of how the Principle of Beneficence can be applied to a
study employing human subjects?
Answer:

Determining that the study
has maximized benefits and minimized risks.

Question:

Which of the following best describes the principle of Respect for Persons as described in the
Belmont Report?
Answer:

Information, comprehension, voluntariness.

Question:

Investigator Obligations in FDA-Regulated Research
Answer:


Question:

When must the investigator update the IRB about the progress of a trial?

, Answer:

During the conduct of the study and at termination

Question:

Form FDA 1572, Statement of Investigator, is legally binding between the investigator and the:
Answer:

FDA

Question:

The investigator must report adverse events to the:
Answer:

Sponser

Question:

In completing Form FDA 1572, Statement of Investigator, the investigator agrees to
Answer:

Conduct or supervise the investigation personally

Question:

Which of the following is an investigator's commitment to the sponsor?
Answer:

Submit a new Form FDA 1572 to the sponsor as needed

Question:

Informed Consent in Clinical Trials of Drugs, Biologics, and Devices
Answer:


Question:

Which of the following statements in a consent form is an example of exculpatory language?
Answer:

I waive any possibility of compensation for injuries that I may
receive as a result of participation in this research.