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Last Updated: Sep 11, 2026
No. of Questions: 127 Questions & Answers with Testing Engine
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ACRP ACRP-CP Exam Syllabus Topics:
| Section | Objectives |
|---|---|
| Topic 1: Participant Safety and Protection | - Informed consent process - Safety reporting and adverse events |
| Topic 2: Clinical Research Foundations | - Good Clinical Practice (GCP) principles - Ethical conduct in clinical trials |
| Topic 3: Data and Quality Management | - Clinical data management principles - Quality assurance and quality control |
| Topic 4: Study Operations | - Study planning and initiation - Study conduct and oversight |
| Topic 5: Regulatory Compliance | - Audit and inspection readiness - Regulatory documentation and submissions |
ACRP Certified Professional Sample Questions:
Which of the following reports should be retained in participant charts?
- A. DSMB/IDMC reports
- B. IRB/IEC progress reports
- C. Lab reports
- D. Safety reports
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AEs that occur between study visits of a clinical trial should be evaluated by the:
- A. Subject's primary care physician
- B. Principal Investigator
- C. Study pharmacovigilance physician
- D. Medical monitor
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A root cause analysis should be:
- A. Written by the investigator.
- B. Specific to a clinical trial.
- C. Focused on issues of non-compliance.
- D. Validated before use in a CAPA.
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Who is responsible for defining, establishing, and allocating all trial-related duties and functions prior to initiating a trial?
- A. IRB/IEC
- B. CRO
- C. Sponsor
- D. Investigator
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Who should vote during the IRB/IEC review and discussion process?
- A. All members who were involved in the review and discussion
- B. All IRB/IEC members and non-member experts
- C. All IRB/IEC members
- D. All members who were involved in the review and discussion and non-member experts
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