ACRP Certified Professional Exam: ACRP-CP Exam

"ACRP Certified Professional Exam", also known as ACRP-CP exam, is a ACRP Certification. With the complete collection of questions and answers, PrepPDF has assembled to take you through 127 Q&As to your ACRP-CP Exam preparation. In the ACRP-CP exam resources, you will cover every field and category in ACRP Certified Professional Certification helping to ready you for your successful ACRP Certification.

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  • Exam Code: ACRP-CP
  • Exam Name: ACRP Certified Professional Exam
  • Certification Provider: ACRP
  • Corresponding Certification: ACRP Certified Professional
  • Updated: Oct 02, 2026
  • No. of Questions: 127 Questions & Answers with Testing Engine
  • Download Limit: Unlimited

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ACRP ACRP-CP Exam Syllabus Topics:

SectionWeightObjectives
Ethical and Participant Safety Considerations19%- Ethical principles
  • 1. Clinical equipoise and therapeutic misconception
  • 2. Human subject protections and privacy
- Clinical care and management of research participants
  • 1. Standard of care vs protocol requirements
  • 2. Informed consent development and review
  • 3. Continuity of medical care
- Safety monitoring and reporting
  • 1. Adverse event identification and classification
  • 2. Safety information evaluation and communication
Data Management and Informatics17%- Data reporting
  • 1. Data integrity and security
  • 2. Database lock and data transfer
- Data collection
  • 1. Electronic data capture systems
  • 2. Case report form design and completion
- Data quality control
  • 1. Query management and resolution
  • 2. Data validation and cleaning
Regulatory and Compliance Requirements17%- International standards
  • 1. Declaration of Helsinki
- Compliance procedures
  • 1. Regulatory submissions and approvals
  • 2. Audits and inspections
- ICH Guidelines
  • 1. E11 Pediatric Trials
  • 2. E8 General Considerations for Clinical Trials
  • 3. E6(R2)/E6(R3) Good Clinical Practice
  • 4. E9 Statistical Principles
  • 5. E2A Expedited Reporting
Clinical Study Operations15%- Site management
  • 1. Site personnel training and delegation
  • 2. Study documentation and record keeping
- Project management
  • 1. Vendor and stakeholder management
  • 2. Timeline and budget management
Study Design and Conduct17%- Study implementation
  • 1. Investigational product management
  • 2. Site selection and activation
  • 3. Study monitoring and oversight
- Study planning
  • 1. Sample size and statistical considerations
  • 2. Protocol development and amendments
  • 3. Study population and eligibility criteria
Professionalism and Ethical Practice15%- Professional standards
  • 1. Role responsibilities and boundaries
  • 2. Confidentiality and conflict of interest
- Continuous improvement
  • 1. Quality assurance and process improvement
  • 2. Professional development and education

ACRP Certified Professional Sample Questions:

The PI may assign responsibility for IP accountability to the pharmacist provided they are:

  • A. Licensed to practice medicine.
  • B. Approved by the IRB/IEC.
  • C. Under the supervision of the PI.
  • D. An employee of the institution.
Reveal Solution  Discussion  0

Correct Answer: C  🗳️

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A sponsor wants to transfer duties to a CRO. Which of the following statements is the MOST correct?

  • A. The IRB/IEC must approve the transfer of duties to a CRO.
  • B. Any trial-related duties can be documented as transferred by verbal agreement.
  • C. All duties transferred to a CRO should be specified in writing.
  • D. Regulatory authorities must be notified promptly of the transfer of any duties to a CRO.
Reveal Solution  Discussion  0

Correct Answer: C  🗳️

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Who determines the age of assent for pediatric studies?

  • A. PI
  • B. IRB/IEC
  • C. Sponsor
  • D. Parent
Reveal Solution  Discussion  0

Correct Answer: B  🗳️

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Which document confirms the PI's agreement to permit auditing at the study site?

  • A. ICF
  • B. Delegation Log
  • C. IB
  • D. Protocol
Reveal Solution  Discussion  0

Correct Answer: A  🗳️

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The sponsor calls the site and informs the research team that they have decided to temporarily suspend the study. What step should the research team take FIRST?

  • A. Inform the IRB/IEC of the study closure.
  • B. Schedule participant for early termination visit.
  • C. Inform the monitor of the termination of the study.
  • D. Inform participant and assure proper care is provided.
Reveal Solution  Discussion  0

Correct Answer: D  🗳️

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