ACRP ACRP-CP actual dump : ACRP Certified Professional Exam

ACRP-CP
  • Exam Code: ACRP-CP
  • Exam Name: ACRP Certified Professional Exam
  • Updated: Sep 19, 2026
  • Q & A: 127 Questions and Answers

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ACRP ACRP-CP Exam Syllabus Topics:

SectionObjectives
Topic 1: Study Operations- Study conduct and oversight
- Study planning and initiation
Topic 2: Data and Quality Management- Quality assurance and quality control
- Clinical data management principles
Topic 3: Participant Safety and Protection- Informed consent process
- Safety reporting and adverse events
Topic 4: Regulatory Compliance- Regulatory documentation and submissions
- Audit and inspection readiness
Topic 5: Clinical Research Foundations- Good Clinical Practice (GCP) principles
- Ethical conduct in clinical trials

ACRP Certified Professional Sample Questions:

Question #1

While reviewing reports of data completion, the sponsor notices low retention rates at many participating sites. What is an appropriate FIRST action for the sponsor to take?

  • A. Submit revised ICFs to the IRB/IEC with increased compensation for participants.
  • B. Meet with the site staff to understand their workflows and to review retention strategies.
  • C. Interview participants who have dropped out.
  • D. Require participants to provide documented reason for withdrawal.
Reveal Solution  Discussion  0

Correct Answer: B  🗳️

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Question #2

Centralized monitoring can:

  • A. Identify IP accountability and storage issues.
  • B. Confirm why sites are deviating from the protocol.
  • C. Enable appropriate stratification of subject enrollment.
  • D. Indicate the need to send monitors to perform onsite visits.
Reveal Solution  Discussion  0

Correct Answer: D  🗳️

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Question #3

Which of the following should be reviewed and evaluated by qualified experts to assess implications for the safety of the trial subjects?

  • A. Sample collection storage, disposal, and shipment requirements
  • B. Emerging animal toxicological and clinical data
  • C. Project feasibility considerations
  • D. PI roles and responsibilities
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Correct Answer: B  🗳️

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Question #4

The objective of a randomized clinical trial is to look at whether an IP is effective in preventing recurrence of a disease. What would be a possible primary endpoint of the trial?

  • A. Use of concomitant medications to treat the symptoms
  • B. Impact of an approved vaccine against the disease
  • C. Occurrence of known side effects of the IP
  • D. Time to occurrence of symptoms of the disease
Reveal Solution  Discussion  0

Correct Answer: D  🗳️

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Question #5

Who should vote during the IRB/IEC review and discussion process?

  • A. All IRB/IEC members
  • B. All members who were involved in the review and discussion and non-member experts
  • C. All IRB/IEC members and non-member experts
  • D. All members who were involved in the review and discussion
Reveal Solution  Discussion  0

Correct Answer: D  🗳️

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