ACRP ACRP-CP - ACRP Certified Professional Exam
- Exam Code: ACRP-CP
- Exam Name: ACRP Certified Professional Exam
- Updated: Nov 08, 2026
- Q & A: 127 Questions and Answers
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| Section | Objectives |
|---|---|
| Topic 1: Data Management and Documentation | - Data integrity
|
| Topic 2: Clinical Trial Operations | - Study start-up activities
|
| Topic 3: Quality Management | - Risk management
|
| Topic 4: Professional Responsibilities | - Leadership and professionalism
|
| Topic 5: Ethical and Participant Safety Considerations | - Human subject protection
|
Access to study documentation for auditors and inspectors during an audit or inspection at a clinical trial site is the responsibility of the:
Correct Answer: D 🗳️
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A printed, optical, or electronic document designed to record all of the protocol-required information and is transmitted to the sponsor is called a:
Correct Answer: C 🗳️
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All of the following are steps to assure an effective risk management approach while conducting a clinical study EXCEPT:
Correct Answer: C 🗳️
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The CRC is prepared to consent a cognitively impaired participant to an Alzheimer's clinical trial. The CRC is required to utilize which of the following in the consent process?
Correct Answer: B 🗳️
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A protocol inclusion criterion requires the serum magnesium at screening to be within the normal range. After the subject received IP, the CRC discovers the subject's screening magnesium level was below the normal range and the sub-investigator marked the lab sheet as not clinically significant. Which of the following should be done FIRST?
Correct Answer: D 🗳️
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