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ACRP ACRP-CP Exam Syllabus Topics:
| Section | Objectives |
|---|---|
| Data Management and Documentation | - Clinical trial documentation
|
| Quality Management | - Risk management
|
| Professional Responsibilities | - Communication and collaboration
|
| Ethical and Participant Safety Considerations | - Human subject protection
|
| Clinical Trial Operations | - Study start-up activities
|
ACRP Certified Professional Sample Questions:
When designing a clinical trial, why is it important to define the study population?
- A. To determine the study objectives
- B. To support the study objectives
- C. To support subject recruitment to the study
- D. To determine where to conduct the study
Correct Answer: B 🗳️
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A clinical trial where participants will be randomized to receive a sequence of two medications has which design configuration?
- A. Factorial
- B. Parallel Group
- C. Crossover
- D. Group sequential
Correct Answer: C 🗳️
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Who must be blinded in a double-blind study in order to prevent bias?
- A. IRB/IEC
- B. Data entry staff
- C. Subject
- D. Pharmacist
Correct Answer: C 🗳️
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The PI may assign responsibility for IP accountability to the pharmacist provided they are:
- A. Approved by the IRB/IEC.
- B. Licensed to practice medicine.
- C. An employee of the institution.
- D. Under the supervision of the PI.
Correct Answer: D 🗳️
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A clinical trial is conducted to measure the effectiveness of music therapy to reduce anxiety in intensive care unit patients. Patients are randomly assigned to receive headphones with music of their choice or headphones with white noise. The group receiving the white noise headphones is considered which type of control group?
- A. Placebo
- B. Active control
- C. No treatment
- D. Alternate dose
Correct Answer: A 🗳️
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