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 License: Complete Roadmap
Follow this path to organize your licensing and exam preparation
Master ICH E6 GCP GuidelinesYou are here
Read the full ICH E6(R2) guideline and create summary notes. This is the primary reference for 100% of exam content. Begin reviewing E6(R3) for the July 2026 transition.
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 48% 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
8-12 weeks of focused study
From start to license in hand
Retake Policy
Candidates who do not pass may retake during the next testing window by paying the exam fee. After two unsuccessful attempts, a new full application and all fees are required.
Total Cost Breakdown
Free ACRP-CP Prep Tools
100 Practice Questions
Covers all 6 ACRP-CP content domains weighted to match the official exam blueprint
AI-Powered Hints
Get contextual hints and wrong-answer explanations powered by AI
Updated for 2026
Reflects ICH E6(R2) with E6(R3) transition guidance for July 2026
100% Free
All 100 practice questions are free — no account required
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
GCP principles, protocol compliance, monitoring activities, essential documents, and quality management systems
Site selection and feasibility, subject recruitment and retention, visit activities, vendor management, and study close-out
Informed consent, IRB/IEC requirements, adverse event reporting, vulnerable populations, and Declaration of Helsinki
IP accountability, storage and handling, blinding procedures, regulatory submissions, and IND/IDE requirements
EDC systems, data collection and validation, query resolution, coding dictionaries, and database lock procedures
Clinical trial phases, randomization, blinding, endpoints, biostatistics, and protocol design
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
More Free Resources
Ready to Start Your Free ACRP-CP Prep?
Review the study guide, practice key concepts, and use the free tools at your own pace.