Free Practice ACRP ACRP-CP Exam Questions 2025

Stay ahead with 100% Free ACRP Certified Professional ACRP-CP Dumps Practice Questions

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Total 127 Questions | Updated On: Jun 03, 2025

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Question 1

An interim analysis is conducted during a clinical trial. To review the results, the sponsor assigns:

A : Executive board members.

B : Independent qualified individuals.

C : Regulatory authority expert advisors.

D : Investigators participating in the trial.

Answer: B

Question 2

Prior to initiation of a clinical trial, review by an IRB/IEC is required for which of the following documents?

A : Protocol, informed consent, and clinical trial agreement

B : IB, site coordinator CVs, and information about payments and compensation available to subjects

C : Protocol, IB, and information about payments and compensation available to subjects

D : Protocol, site coordinator CVs, and clinical trial agreement

Answer: C

Question 3

Which of the following should be considered when implementing a risk-based monitoring plan?

A : 100% source document review is mandatory.

B : Centralized monitoring must be incorporated in any trials.

C : Monitoring schedule must be pre-defined in the monitoring plan.

D : On-site monitoring frequency may change depending on the quality of the data.

Answer: D

Question 4

Prior to initiation of a clinical trial, review by an IRB/IEC is required for which of the following documents?

A : Protocol, informed consent, and clinical trial agreement

B : IB, site coordinator CVs, and information about payments and compensation available to subjects

C : Protocol, IB, and information about payments and compensation available to subjects

D : Protocol, site coordinator CVs, and clinical trial agreement

Answer: C

Question 5

Which document confirms the PI’s agreement to permit auditing at the study site?

A : IB

B : ICF

C : Protocol

D : Delegation Log

Answer: B

Page: 1 / 26

Total 127 Questions | Updated On: Jun 03, 2025

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