Free ACRP-CP Questions for ACRP Certified Professional ACRP-CP Exam as PDF & Practice Test Engine

Exam Code/Number: ACRP-CP
Exam Name/Title: ACRP Certified Professional Exam
Certification Provider: ACRP
Corresponding Certification: ACRP Certified Professional

Exam Questions: 127
Updated On: Oct 07, 2026

Question #1

Who is responsible for outlining written procedures in a study to assure that changes or corrections in CRFs are documented, are necessary, and are endorsed by the investigator?

A. Data Manager

B. CRO

C. CRA

D. Sponsor

Discussion 0

Correct Answer: D Vote an answer

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Question #2

The sponsor calls the site and informs the research team that they have decided to temporarily suspend the study. What step should the research team take FIRST?

A. Schedule participant for early termination visit.

B. Inform participant and assure proper care is provided.

C. Inform the monitor of the termination of the study.

D. Inform the IRB/IEC of the study closure.

Discussion 0

Correct Answer: B Vote an answer

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Question #3

The investigator/institution should permit:

A. Monitoring and inspection by the sponsor, and auditing by the appropriate regulatory authority(ies).

B. Monitoring and auditing by the appropriate regulatory authority(ies), and inspection by the sponsor.

C. Monitoring and inspection by the appropriate regulatory authority(ies), and auditing by the sponsor.

D. Monitoring and auditing by the sponsor, and inspection by the appropriate regulatory authority(ies).

Discussion 0

Correct Answer: C Vote an answer

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Question #4

SAEs must be reported immediately by the site to the:

A. DSMB/IDMC.

B. IRB/IEC.

C. Regulatory agency.

D. Sponsor.

Discussion 0

Correct Answer: D Vote an answer

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Question #5

A study to determine the effective dose and regimen of a new IP for the treatment of hypothyroidism is considered to be:

A. Phase III

B. Phase II

C. Phase IV

D. Phase I

Discussion 0

Correct Answer: B Vote an answer

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Question #6

The PI did not record the relationship to IP in the medical chart when assessing an adverse event. The CRC noticed the omission and brought it to the PI's attention. How should this be addressed?

A. The PI should amend the medical chart.

B. The CRC should amend the medical chart.

C. The PI should notify the monitor.

D. The CRC should write a note to file.

Discussion 0

Correct Answer: A Vote an answer

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Question #7

A clinical trial is conducted to test the effect of an investigational drug on cholesterol levels. Statistical analysis will be performed to:

A. Reject the null hypothesis that the drug has no effect on cholesterol levels.

B. Fail to reject the alternative hypothesis that the drug has an effect on cholesterol levels.

C. Fail to reject the null hypothesis that the drug has an effect on cholesterol levels.

D. Reject the alternative hypothesis that the drug has no effect on cholesterol levels.

Discussion 0

Correct Answer: A Vote an answer

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Question #8

In addition to members who collectively have the qualifications and experience to review and evaluate the science, medical aspects, and ethics of the proposed trial, it is recommended that the IRB/IEC should include:

A. A total of five members.

B. One member of the site's QA group.

C. One member whose primary area of interest is in the same scientific area.

D. One member who is independent of the institution/trial site.

Discussion 0

Correct Answer: D Vote an answer

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Free ACRP-CP Questions for ACRP Certified Professional ACRP-CP Exam as PDF & Practice Test Engine

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