ACRP-CP exam dumps

ACRP ACRP-CP Value Package

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  • Exam Code: ACRP-CP
  • Exam Name: ACRP Certified Professional Exam
  • No. of Questions: 127 Questions and Answers
  • Updated: Sep 20, 2026

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ACRP ACRP-CP Exam Syllabus Topics:

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

ACRP Certified Professional Sample Questions:

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

Correct Answer: A  🗳️

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A deferred consent can take place in which of the following situations?

  • A. Only when the PI approves such a consent process immediately prior to patient enrollment, regardless of the situation being classed as emergency.
  • B. In an emergency situation only, when this process is described in the protocol and has received permission from the ethics committee.
  • C. Only when the PI approves such a consent process, regardless of the emergency situation described in the protocol.
  • D. In an emergency situation only, even when this process is not described in the protocol, but the sponsor approves the consent process.
Reveal Solution  Discussion  0

Correct Answer: B  🗳️

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The coding system for a double-blind clinical trial is accessible by the:

  • A. Sponsor
  • B. Regulatory authority
  • C. PI
  • D. IRB/IEC
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Correct Answer: A  🗳️

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One key attribute for good study documentation is that the data are contemporaneous, which refers to the practice of:

  • A. Recording the date and time each data element is entered onto the source document.
  • B. Allowing real-time access for data review in the eCRF.
  • C. Recording data on source documents at the time the data are collected during the conduct of the study.
  • D. Comparing source document data to other data recorded in the same study time period.
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Correct Answer: C  🗳️

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A clinical trial is conducted to test the effect of an investigational drug on cholesterol levels. Statistical analysis will be performed to:

  • A. Reject the null hypothesis that the drug has no effect on cholesterol levels.
  • B. Fail to reject the alternative hypothesis that the drug has an effect on cholesterol levels.
  • C. Fail to reject the null hypothesis that the drug has an effect on cholesterol levels.
  • D. Reject the alternative hypothesis that the drug has no effect on cholesterol levels.
Reveal Solution  Discussion  0

Correct Answer: A  🗳️

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