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ACRP ACRP-CP Exam Syllabus Topics:
| Section | Objectives |
|---|---|
| Topic 1: Clinical Trial Operations | - Study conduct
|
| Topic 2: Quality Management | - Audit and inspection readiness
|
| Topic 3: Ethical and Participant Safety Considerations | - Human subject protection
|
| Topic 4: Data Management and Documentation | - Clinical trial documentation
|
| Topic 5: Professional Responsibilities | - Communication and collaboration
|
ACRP Certified Professional Sample Questions:
Question 1
Centralized monitoring can:
A. Indicate the need to send monitors to perform onsite visits.
B. Enable appropriate stratification of subject enrollment.
C. Confirm why sites are deviating from the protocol.
D. Identify IP accountability and storage issues.
Question 2
The primary purpose for IRB/IEC approval of posters, fliers, social media posts, and promotional items is to:
A. Confirm subjects receive the appropriate reimbursement.
B. Assure the ads do not impinge on confidentiality agreements.
C. Review the content for ethically or morally sensitive issues.
D. Safeguard the rights, safety, and well-being of all potential subjects.
Question 3
Which document confirms the PI's agreement to permit auditing at the study site?
A. Delegation Log
B. IB
C. Protocol
D. ICF
Question 4
The IRB/IEC has decided to not approve a clinical trial. Who must they notify in writing?
A. Sponsor
B. Regulatory Agency
C. PI
D. CRC
Question 5
In order to conduct open-label, parallel group clinical trials according to sound scientific principles, which of the following design elements should be included?
A. Privacy controls
B. Blinding
C. Placebo-controlled
D. Randomization
Solutions:
| Question 1 Answer: A | Question 2 Answer: D | Question 3 Answer: D | Question 4 Answer: C | Question 5 Answer: D |






