ACRP ACRP-CP Questions & Answers - in .pdf
- Total Q&A: 127
- Update: Aug 15, 2026
- Price: $59.99
- Vendor: ACRP
- Exam Code: ACRP-CP
- Exam Name: ACRP Certified Professional Exam
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ACRP ACRP-CP Exam Syllabus Topics:
| Section | Objectives |
|---|
| Quality Management | - Audit and inspection readiness
- 1. Compliance monitoring
- 2. Inspection preparation
- Risk management
- 1. Quality assurance
- 2. Corrective and preventive actions
|
| Clinical Trial Operations | - Study conduct
- 1. Participant management
- 2. Safety reporting
- Study start-up activities
- 1. Protocol implementation
- 2. Site preparation
|
| Professional Responsibilities | - Communication and collaboration
- 1. Stakeholder communication
- 2. Cross-functional teamwork
- Leadership and professionalism
- 1. Decision making
- 2. Professional ethics
|
| Ethical and Participant Safety Considerations | - Human subject protection
- 1. Informed consent
- 2. Participant rights
- Regulatory compliance
- 1. ICH GCP adherence
- 2. IRB and ethics requirements
|
| Data Management and Documentation | - Data integrity
- 1. Query resolution
- 2. Data collection
- Clinical trial documentation
- 1. Source documentation
- 2. Essential documents
|
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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