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Exam Code: ACRP-CP
Exam Name: ACRP Certified Professional Exam
Updated: Aug 07, 2026
Q & A: 127 Questions and Answers
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| Section | Objectives |
|---|---|
| Study Operations | - Study conduct and oversight - Study planning and initiation |
| Clinical Research Foundations | - Good Clinical Practice (GCP) principles - Ethical conduct in clinical trials |
| Participant Safety and Protection | - Informed consent process - Safety reporting and adverse events |
| Regulatory Compliance | - Regulatory documentation and submissions - Audit and inspection readiness |
| Data and Quality Management | - Quality assurance and quality control - Clinical data management principles |
1. An impartial witness should be present during the entire informed consent discussion when:
A) An interpreter is translating the consent form for a subject.
B) A subject has been determined to be vulnerable.
C) A parent/guardian is consenting for a minor subject.
D) A legally acceptable representative is unable to read.
2. A PI is being considered for an industry-sponsored study. The PI sees approximately 20 patients per month who meet the study criteria. The PI does not have access to a Positron Emission Tomography (PET) scanner, which is required for the protocol. The PI is already taking part in three other studies. Should the Sponsor choose this PI?
A) No, the PI does not have the resources to perform all protocol-required procedures.
B) Yes, the PI has a sufficient patient population to take part in this study.
C) Yes, the PI can perform other imaging scans instead of the PET scans.
D) No, the PI is taking part in too many ongoing studies to participate in this study.
3. A study is using an EDC system. After the data is entered into EDC, who is the next to review and conduct SDV of this data?
A) QA Department
B) Data Manager
C) Monitor
D) Sponsor
4. IP is dispensed to all subjects who:
A) Consented for the trial.
B) Need IP for their medical condition.
C) Are eligible to receive it in the trial.
D) Screened for the trial.
5. A study to determine the effective dose and regimen of a new IP for the treatment of hypothyroidism is considered to be:
A) Phase IV
B) Phase III
C) Phase II
D) Phase I
Solutions:
| Question # 1 Answer: D | Question # 2 Answer: A | Question # 3 Answer: C | Question # 4 Answer: C | Question # 5 Answer: C |
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