Free ACRP-CP Exam Prep
ACRP Certified Professional (ACRP-CP)
Prepare for the ACRP-CP exam without spending hundreds on expensive prep courses. Free study guides, practice questions, flashcards, and related exam resources.
Quick Facts
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ACRP-CP ACRP Clinical Research Certifications: Study Roadmap
Follow this path to organize your exam preparation
Master ICH E6 GCP GuidelinesYou are here
Read the full ICH E6(R3) guideline and create summary notes. It replaced E6(R2) on ACRP exams from July 15, 2026 and is the main GCP reference, alongside E2A, E8(R1), E9, E9(R1), E11(R1) and the Declaration of Helsinki.
Study Ethics, Safety, and Regulatory Content
Review ICH E2A (expedited reporting), Declaration of Helsinki, informed consent processes, and IRB/IEC requirements. These domains make up 35% of the exam.
Focus on Clinical Operations and Site Management
Study essential documents, monitoring procedures, site management activities, and quality systems. These two domains account for 46% of the exam.
Practice Questions and Review
Take full-length timed practice exams, review weak areas, and ensure familiarity with the scenario-based question format.
Can You Take the ACRP-CP Exam?
Check if you meet the basic eligibility requirements
- •Work must be through a paid employer/employee arrangement (internships excluded)
- •Experience must be within the last 10 years
- •Up to 1,500 hours may be waived with an active ACRP certification or accredited education program
- •Evidence through detailed job description, CV, or documentation of involvement in planning, conducting, or overseeing clinical trials
ACRP-CP Quick Facts
Time to Get Licensed
From start to license in hand
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Total Cost Breakdown
Free ACRP-CP Prep Tools
100 Practice Questions
Covers ethics, GCP operations, site management, research design and data topics tested on the ACRP-CP
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Get contextual hints and wrong-answer explanations powered by AI
Updated for 2026
ACRP exams have used ICH E6(R3) since July 15, 2026
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What You'll Study
13 chapters covering the exam topics in this guide
Chapter 1: GCP Principles, Roles & Delegation
4 sections
Chapter 2: Essential Records, Source Documentation & Data Confidentiality
4 sections
Chapter 3: Monitoring, Quality Management & Audits
4 sections
Chapter 4: Site Feasibility, Start-Up, Facilities & Laboratory Operations
6 sections
Chapter 5: Subject Recruitment, Retention & Study Visits
4 sections
Chapter 6: Protocol Compliance, Deviations & Site Close-Out
3 sections
Chapter 7: Research Ethics, Vulnerable Populations & Research Integrity
4 sections
Chapter 8: Informed Consent & Institutional Review Boards (IRB/IEC)
3 sections
Chapter 9: Safety Reporting & Adverse Event Management (ICH E2A)
3 sections
Chapter 10: Investigational Product (IP) Management & Accountability
4 sections
Chapter 11: Regulatory Frameworks, Submissions & Product Reference Information
4 sections
Chapter 12: Clinical Data Management, EDC & Electronic Records
4 sections
Chapter 13: Trial Design, Biostatistics, Data Monitoring & Transparency
6 sections
ACRP-CP Exam Details
ACRP Certified Professional (ACRP-CP)
Administered by Association of Clinical Research Professionals (ACRP)
Exam Content Breakdown
Based on the official Association of Clinical Research Professionals (ACRP) content outline
Standard of care versus protocol requirements, equipoise, vulnerable populations, informed consent and assent, protocol deviations, safety monitoring and reporting, conflicts of interest, and fraud and misconduct
Stakeholders and regulatory frameworks, phases of clinical research, regulatory and safety reporting, hazardous goods and samples, audits and inspections, IRB/IEC role, protocol approval and amendments, and interim analysis or DSMB milestones
Trial conduct and documentation, staff roles and delegation, investigational product control, adverse event management and reporting, monitoring, audits, deviations, CAPA, source data review, PI responsibilities, and site initiation through closeout
Quality management, oversight by PIs, sponsors and CROs, budgets and agreements, equipment, product accountability, non-compliance, sample handling, subject compliance, feasibility, record retention, and essential documents such as the trial master file
Trial design and randomization, protocol and Investigator’s Brochure elements, eligibility, objectives and endpoints, biostatistics and informatics, data flow, collection, corrections and queries, data quality and privacy, and ALCOA-C documentation
What's Included
13 Chapters
Complete exam coverage
Practice Quizzes
With detailed explanations
Free to Start
No credit card required
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What's Next After the ACRP-CP?
After passing the ACRP-CP, you can pursue these career paths
CCRC
Certified Clinical Research Coordinator for site-specific coordination roles
CCRA
Certified Clinical Research Associate for monitoring and CRA roles
ACRP-PM
ACRP Project Manager specialty add-on credential (requires existing ACRP cert)
ACRP-MDP
ACRP Medical Device Professional specialty add-on credential (requires existing ACRP cert)
ACRP-CP Exam FAQ
Official Association of Clinical Research Professionals (ACRP) Resources
Verify information with these official sources
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Ready to Start Your Free ACRP-CP Prep?
Review the study guide, practice key concepts, and use the free tools at your own pace.