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Last Updated: Oct 09, 2026
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ACRP ACRP-CP Exam Syllabus Topics:
| Section | Objectives |
|---|---|
| Topic 1: Clinical Trial Operations | - Study conduct
|
| Topic 2: Data Management and Documentation | - Clinical trial documentation
|
| Topic 3: Quality Management | - Audit and inspection readiness
|
| Topic 4: Professional Responsibilities | - Communication and collaboration
|
| Topic 5: Ethical and Participant Safety Considerations | - Human subject protection
|
ACRP Certified Professional Sample Questions:
AEs that occur between study visits of a clinical trial should be evaluated by the:
- A. Study pharmacovigilance physician
- B. Medical monitor
- C. Principal Investigator
- D. Subject's primary care physician
Correct Answer: C 🗳️
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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. CRF.
- C. PRO.
- D. Worksheet.
Correct Answer: B 🗳️
Explanation: Only visible for Actualtests4sure members. You can sign-up / login (it's free).
In a quality management system, in which category do risk reduction activities belong?
- A. Risk Communication
- B. Risk Control
- C. Risk Evaluation
- D. Risk Review
Correct Answer: B 🗳️
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Which document confirms the PI's agreement to permit auditing at the study site?
- A. Protocol
- B. Delegation Log
- C. IB
- D. ICF
Correct Answer: D 🗳️
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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. Conduct annual reviews of the protocol and accompanying study documents.
- C. Develop a plan that describes the monitoring approach for a clinical study.
- D. Ensure there is an accompanying written record that describes the consent process.
Correct Answer: C 🗳️
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