ACRP ACRP-CP Actual Free Exam Questions & Community Discussion

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: Jun 03, 2026

Question #29

A hospital site is being considered for a trial that requires the IP refrigerator to be continuously monitored using the sponsor-provided Wi-Fi-enabled thermometer. The hospital's Wi-Fi connectivity is inconsistent.
During site selection, how should the CRA proceed?

A. Before accepting this site, report the risk to the trial sponsor and await their decision.

B. Accept this site and plan to undertake routine safety evaluations of the IP.

C. Accept this site and implement and maintain QA and QC systems with written SOPs.

D. Before accepting this site, ensure the refrigerator is calibrated and functioning properly.

Discussion 0

Correct Answer: A Vote an answer

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Question #30

A Phase I drug trial has been completed and preparations are being made to proceed to a Phase II trial. Who is responsible for revising the IB with this updated information?

A. DSMB/IDMC

B. Sponsor

C. Investigator

D. Health authority

Discussion 0

Correct Answer: B Vote an answer

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Question #31

A sponsor wants a new clinical trial to be reviewed at regular intervals for progress, safety, and endpoint evaluation, and make recommendations to continue, modify, or stop the trial. How should they proceed?

A. Establish a DSMB/IDMC

B. Draft a CAPA plan

C. Develop a monitoring plan

D. Conduct routine investigators' meetings

Discussion 0

Correct Answer: A Vote an answer

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Question #32

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

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

C. A total of five members.

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

Discussion 0

Correct Answer: A Vote an answer

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Question #33

A study subject inadvertently disposed of IP medication bottles. The site should report this to the:

A. Sponsor.

B. IRB/IEC.

C. Medical monitor.

D. Regulatory authority.

Discussion 0

Correct Answer: A Vote an answer

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Question #34

Which of the following documents is maintained by a PI to ensure compliance with sponsor requirements?

A. A monitoring plan that is tailored to the specific human subject protection and data integrity risks of the trial.

B. Training records of site personnel on study protocol, and their study-related duties and functions.

C. Regulatory submission of protocol and accompanying documents to relevant regulatory authority.

D. A monitoring report that identifies deviation from the approved protocol.

Discussion 0

Correct Answer: B Vote an answer

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Question #35

In preparation for an upcoming site audit, whose responsibility is it to ensure study-related functions were conducted by qualified personnel?

A. CRC

B. CRA

C. Sponsor

D. Investigator

Discussion 0

Correct Answer: D Vote an answer

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