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Last Updated: Oct 30, 2026

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ACRP ACRP-CP Practice Q&A's

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Lifelong learning is no longer a slogan; it is a career strategy. PracticeMaterial furthers that strategy for ACRP Certified Professional candidates with 127 verified ACRP-CP practice questions, refined by professional expert teams.

ACRP ACRP-CP Exam Syllabus Topics:

SectionWeightObjectives
Topic 1: Clinical Study Operations15%- Site management
  • 1. Study documentation and record keeping
  • 2. Site personnel training and delegation
- Project management
  • 1. Timeline and budget management
  • 2. Vendor and stakeholder management
Topic 2: Ethical and Participant Safety Considerations19%- Ethical principles
  • 1. Clinical equipoise and therapeutic misconception
  • 2. Human subject protections and privacy
- Safety monitoring and reporting
  • 1. Safety information evaluation and communication
  • 2. Adverse event identification and classification
- Clinical care and management of research participants
  • 1. Informed consent development and review
  • 2. Continuity of medical care
  • 3. Standard of care vs protocol requirements
Topic 3: Study Design and Conduct17%- Study implementation
  • 1. Investigational product management
  • 2. Study monitoring and oversight
  • 3. Site selection and activation
- Study planning
  • 1. Sample size and statistical considerations
  • 2. Study population and eligibility criteria
  • 3. Protocol development and amendments
Topic 4: Professionalism and Ethical Practice15%- Continuous improvement
  • 1. Quality assurance and process improvement
  • 2. Professional development and education
- Professional standards
  • 1. Confidentiality and conflict of interest
  • 2. Role responsibilities and boundaries
Topic 5: Data Management and Informatics17%- Data collection
  • 1. Case report form design and completion
  • 2. Electronic data capture systems
- Data quality control
  • 1. Data validation and cleaning
  • 2. Query management and resolution
- Data reporting
  • 1. Database lock and data transfer
  • 2. Data integrity and security
Topic 6: 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. E2A Expedited Reporting
  • 3. E6(R2)/E6(R3) Good Clinical Practice
  • 4. E9 Statistical Principles
  • 5. E8 General Considerations for Clinical Trials

ACRP Certified Professional Questions, Answered by Experience

ACRP Certified Professional is an official Association of Clinical Research Professionals (ACRP) certification exam, listed under the code ACRP-CP. Passing it earns the ACRP Certified Professional certification at the Professional level. It also ties into ACRP Certified Clinical Research Associate (CCRA), ACRP Certified Clinical Research Coordinator (CCRC), ACRP Certified Principal Investigator (CPI). In an era of lifelong learning, this credential is one of the most efficient ways to prove your skills keep pace.

ACRP Certified Professional gives you 125 (100 scored, 25 pre-test) questions across 180 minutes. The efficient approach: one to two hours of daily timed practice in the PracticeMaterial engine builds both the knowledge and the pacing, so exam day feels like simply another well-run session.

Passing ACRP Certified Professional takes Scaled score of 600 or higher, and the official registration fee is $435 – $600. Retakes cost the full $435 – $600 again, so treat your PracticeMaterial practice scores as the decision-maker: book when the passing line sits below your everyday results, not your best ones.

The ACRP Certified Professional syllabus is organized into 6 domains, led by Data Management and Informatics (17%), Regulatory and Compliance Requirements (17%), and Study Design and Conduct (17%). The complete breakdown is above on this page; it is the fastest way to learn where your limited preparation hours belong.

3,000 hours verifiable clinical research work experience; or 1,500 hours plus clinical research degree

Vendor policies are revised periodically, so verify the current requirements before registering via the official exam page.

Registration for ACRP Certified Professional goes through the official channels below.

For planning: the exam is delivered Online remote proctored or in-person at PSI test centers.

Association of Clinical Research Professionals (ACRP) recommends the following training for ACRP Certified Professional candidates.

Follow any training with daily practice on the 127 questions in the PracticeMaterial ACRP-CP package; sorted by authorized expert groups, they turn course theory into exam-ready skill.

Yes on both counts. Download the free demo of the ACRP Certified Professional questions first, and browse the comments written by former customers for a second opinion. After purchase, new versions are sent to you as soon as they release, free for 365 days; after expiry, extending the update service costs 50% of the regular price.

Worry-free means a 100% money-back guarantee with stated conditions. Take the ACRP Certified Professional exam within 60 days of purchase; if you fail, you may claim a full refund, provided the exam matches your product. Attempts within 3 days of purchase are ineligible, as are downloaded-but-unused products, free materials, and expired orders; the candidate name must match the payer name. Submit a scanned enrollment slip and the official Score Report PDF within 2 days of the exam, and claims are processed within 7 days. Alternatively, exchange for two other exam products of equal value, free, keeping the update service on your original purchase.

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ACRP Certified Professional Sample Questions:

Question #1

Which entity has ultimate responsibility over the conduct of the multi-center clinical trial?

  • A. IRB/IEC
  • B. CRO
  • C. Sponsor-Investigator
  • D. Regulatory authority
Reveal Solution  Discussion  0

Correct Answer: C  🗳️

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Question #2

What would a sponsor use to implement and maintain quality in a study?

  • A. Statistical analysis plan
  • B. Standard operating procedures
  • C. Protocol signature pages
  • D. Clinical trial agreement
Reveal Solution  Discussion  0

Correct Answer: B  🗳️

Explanation: Only visible for PracticeMaterial members. You can sign-up / login (it's free).

Question #3

The inclusion and exclusion criteria are in place so all subjects are:

  • A. Medically appropriate and protected from ethical vulnerability.
  • B. Healthy and willing to complete the clinical trial.
  • C. Patients with the disease under study and will not have any adverse events.
  • D. Ethically vulnerable and patients with the disease under study.
Reveal Solution  Discussion  0

Correct Answer: A  🗳️

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Question #4

The sponsor must report a serious unexpected AE to the regulatory authorities within a maximum of:

  • A. 30 calendar days
  • B. 7 calendar days
  • C. 8 calendar days
  • D. 15 calendar days
Reveal Solution  Discussion  0

Correct Answer: D  🗳️

Explanation: Only visible for PracticeMaterial members. You can sign-up / login (it's free).

Question #5

The sponsor should supply a PI with the IP after:

  • A. Submission of documents to IRB/IEC and regulatory authority for review.
  • B. Approval/favorable opinion from IRB/IEC and regulatory authority.
  • C. Approval of protocol by the sponsor.
  • D. Approval of protocol by the PI.
Reveal Solution  Discussion  0

Correct Answer: B  🗳️

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