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Instant Download ACRP : ACRP-CP Questions & Answers as PDF & Test Engine
- Exam Code: ACRP-CP
- Exam Name: ACRP Certified Professional Exam
- Updated: Sep 02, 2026
- No. of Questions: 127 Questions and Answers
- Download Limit: Unlimited
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ACRP ACRP-CP Exam Syllabus Topics:
| Section | Objectives |
|---|---|
| Ethical and Participant Safety Considerations | - Regulatory compliance
|
| Clinical Trial Operations | - Study start-up activities
|
| Professional Responsibilities | - Leadership and professionalism
|
| Quality Management | - Audit and inspection readiness
|
| Data Management and Documentation | - Clinical trial documentation
|
ACRP Certified Professional Sample Questions:
Question 1
In addition to members who collectively have the qualifications and experience to review and evaluate the science, medical aspects, and ethics of the proposed trial, it is recommended that the IRB/IEC should include:
A. One member who is independent of the institution/trial site.
B. A total of five members.
C. One member whose primary area of interest is in the same scientific area.
D. One member of the site's QA group.
Question 2
One key attribute for good study documentation is that the data are contemporaneous, which refers to the practice of:
A. Comparing source document data to other data recorded in the same study time period.
B. Allowing real-time access for data review in the eCRF.
C. Recording the date and time each data element is entered onto the source document.
D. Recording data on source documents at the time the data are collected during the conduct of the study.
Question 3
After enrolling and treating a few subjects on an investigator-initiated trial, the PI would like to include a subject diary for each trial subject to capture their activities and experiences on the trial regimen. After the PI has generated a diary, what should the PI do next?
A. No approval is necessary: give the diary to each subject.
B. Submit the diary to the regulatory authority for approval.
C. Submit the diary to the sponsor for approval.
D. Submit the diary to the IRB/IEC for approval.
Question 4
The PI may assign responsibility for IP accountability to the pharmacist provided they are:
A. Under the supervision of the PI.
B. An employee of the institution.
C. Approved by the IRB/IEC.
D. Licensed to practice medicine.
Question 5
Who determines what criteria and procedures should be followed if a subject discontinues/withdraws their consent?
A. CRO
B. Subject
C. PI
D. Sponsor
Solutions:
| Question 1 Answer: A | Question 2 Answer: D | Question 3 Answer: D | Question 4 Answer: A | Question 5 Answer: D |
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