ACRP ACRP-CP - ACRP Certified Professional Exam

ACRP ACRP-CP Actual PDF
  • Exam Code: ACRP-CP
  • Exam Name: ACRP Certified Professional Exam
  • Updated: Nov 08, 2026
  • Q & A: 127 Questions and Answers
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ACRP ACRP-CP Exam Syllabus Topics:

SectionObjectives
Topic 1: Data Management and Documentation- Data integrity
  • 1. Data collection
  • 2. Query resolution
- Clinical trial documentation
  • 1. Essential documents
  • 2. Source documentation
Topic 2: Clinical Trial Operations- Study start-up activities
  • 1. Site preparation
  • 2. Protocol implementation
- Study conduct
  • 1. Participant management
  • 2. Safety reporting
Topic 3: Quality Management- Risk management
  • 1. Quality assurance
  • 2. Corrective and preventive actions
- Audit and inspection readiness
  • 1. Compliance monitoring
  • 2. Inspection preparation
Topic 4: Professional Responsibilities- Leadership and professionalism
  • 1. Decision making
  • 2. Professional ethics
- Communication and collaboration
  • 1. Stakeholder communication
  • 2. Cross-functional teamwork
Topic 5: Ethical and Participant Safety Considerations- Human subject protection
  • 1. Informed consent
  • 2. Participant rights
- Regulatory compliance
  • 1. ICH GCP adherence
  • 2. IRB and ethics requirements

ACRP Certified Professional Sample Questions:

Question #1

Access to study documentation for auditors and inspectors during an audit or inspection at a clinical trial site is the responsibility of the:

  • A. CRA
  • B. Sponsor
  • C. CRC
  • D. PI
Reveal Solution  Discussion  0

Correct Answer: D  🗳️

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Question #2

A printed, optical, or electronic document designed to record all of the protocol-required information and is transmitted to the sponsor is called a:

  • A. Source document.
  • B. Worksheet.
  • C. CRF.
  • D. PRO.
Reveal Solution  Discussion  0

Correct Answer: C  🗳️

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Question #3

All of the following are steps to assure an effective risk management approach while conducting a clinical study EXCEPT:

  • A. Controlling risk by setting thresholds of risk acceptability.
  • B. Identifying potential study risks.
  • C. Documenting all possible risk scenarios.
  • D. Assessing risk based on study impact.
Reveal Solution  Discussion  0

Correct Answer: C  🗳️

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Question #4

The CRC is prepared to consent a cognitively impaired participant to an Alzheimer's clinical trial. The CRC is required to utilize which of the following in the consent process?

  • A. A witness
  • B. A legally acceptable representative
  • C. A family member
  • D. A member of the research team
Reveal Solution  Discussion  0

Correct Answer: B  🗳️

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Question #5

A protocol inclusion criterion requires the serum magnesium at screening to be within the normal range. After the subject received IP, the CRC discovers the subject's screening magnesium level was below the normal range and the sub-investigator marked the lab sheet as not clinically significant. Which of the following should be done FIRST?

  • A. Notify the regulatory authority.
  • B. Notify the subject.
  • C. Withdraw the subject.
  • D. Notify the sponsor.
Reveal Solution  Discussion  0

Correct Answer: D  🗳️

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