Try ACRP : ACRP-CP valid & accurate questions and answers

Last Updated: Sep 18, 2026

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ACRP ACRP-CP Exam Syllabus Topics:

SectionObjectives
Professional Responsibilities- Communication and collaboration
  • 1. Cross-functional teamwork
  • 2. Stakeholder communication
- Leadership and professionalism
  • 1. Decision making
  • 2. Professional ethics
Quality Management- Audit and inspection readiness
  • 1. Compliance monitoring
  • 2. Inspection preparation
- Risk management
  • 1. Corrective and preventive actions
  • 2. Quality assurance
Data Management and Documentation- Data integrity
  • 1. Data collection
  • 2. Query resolution
- Clinical trial documentation
  • 1. Essential documents
  • 2. Source documentation
Ethical and Participant Safety Considerations- Human subject protection
  • 1. Participant rights
  • 2. Informed consent
- Regulatory compliance
  • 1. ICH GCP adherence
  • 2. IRB and ethics requirements
Clinical Trial Operations- Study conduct
  • 1. Participant management
  • 2. Safety reporting
- Study start-up activities
  • 1. Protocol implementation
  • 2. Site preparation

ACRP Certified Professional Sample Questions:

Question #1

Which of the following activities would be undertaken by the sponsor to BEST ensure overall quality of the study data?

  • A. Ensure submission of a data management plan to the regulatory authorities.
  • B. Develop a plan that describes the monitoring approach for a clinical study.
  • C. Ensure there is an accompanying written record that describes the consent process.
  • D. Conduct annual reviews of the protocol and accompanying study documents.
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Correct Answer: B  🗳️

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Question #2

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

  • A. Protocol, IB, and information about payments and compensation available to subjects
  • B. IB, site coordinator CVs, and information about payments and compensation available to subjects
  • C. Protocol, site coordinator CVs, and clinical trial agreement
  • D. Protocol, informed consent, and clinical trial agreement
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Correct Answer: A  🗳️

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Question #3

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

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Question #4

Which one of the following is a primary objective of a Phase III study of a new IP?

  • A. To establish the safety profile
  • B. To demonstrate or confirm therapeutic benefit
  • C. To establish dose information
  • D. To show superiority over another treatment
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Correct Answer: B  🗳️

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Question #5

Confidentiality and privacy rules for protection of human subjects at research sites are determined by the:

  • A. Applicable regulatory authorities
  • B. Sponsor
  • C. Applicable site SOPs
  • D. PI
Reveal Solution  Discussion  0

Correct Answer: A  🗳️

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