ACRP ACRP-CP Questions & Answers - in .pdf
- Total Q&A: 127
- Update: Jul 04, 2026
- Price: $59.99
- Vendor: ACRP
- Exam Code: ACRP-CP
- Exam Name: ACRP Certified Professional Exam
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ACRP Certified Professional Sample Questions:
1. 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) Worksheet.
B) Source document.
C) CRF.
D) PRO.
2. After the site qualification visit report has been finalized, it must be:
A) Included in the PI's regulatory file.
B) Sent to the IRB/IEC for review and approval.
C) Stored in the sponsor's budgets and contracts file.
D) Kept in the CRO/sponsor's trial master file.
3. A study subject inadvertently disposed of IP medication bottles. The site should report this to the:
A) Sponsor.
B) Regulatory authority.
C) IRB/IEC.
D) Medical monitor.
4. Which of the following would the sponsor need to do FIRST to set up an effective clinical trial quality management system (QMS)?
A) Perform a periodic review to see if the quality methods are effective and relevant.
B) Identify critical processes and data during protocol development.
C) Determine the quality tolerance limits for data transcription errors.
D) Train the research coordinator on the required study assessments schedule.
5. A Phase I drug trial has been completed and preparations are being made to proceed to a Phase II trial. Who is responsible for revising the IB with this updated information?
A) Health authority
B) Sponsor
C) DSMB/IDMC
D) Investigator
Solutions:
Question # 1
Answer: C | Question # 2
Answer: D | Question # 3
Answer: A | Question # 4
Answer: B | Question # 5
Answer: B |
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