- Exam Code: ACRP-CP
- Exam Name: ACRP Certified Professional Exam
- Updated: Sep 19, 2026
- Q & A: 127 Questions and Answers
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| Section | Objectives |
|---|---|
| Topic 1: Study Operations | - Study conduct and oversight - Study planning and initiation |
| Topic 2: Data and Quality Management | - Quality assurance and quality control - Clinical data management principles |
| Topic 3: Participant Safety and Protection | - Informed consent process - Safety reporting and adverse events |
| Topic 4: Regulatory Compliance | - Regulatory documentation and submissions - Audit and inspection readiness |
| Topic 5: Clinical Research Foundations | - Good Clinical Practice (GCP) principles - Ethical conduct in clinical trials |
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?
Correct Answer: B 🗳️
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Centralized monitoring can:
Correct Answer: D 🗳️
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Which of the following should be reviewed and evaluated by qualified experts to assess implications for the safety of the trial subjects?
Correct Answer: B 🗳️
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The objective of a randomized clinical trial is to look at whether an IP is effective in preventing recurrence of a disease. What would be a possible primary endpoint of the trial?
Correct Answer: D 🗳️
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Who should vote during the IRB/IEC review and discussion process?
Correct Answer: D 🗳️
Explanation: Only visible for Actual4Dumps members. You can sign-up / login (it's free).
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