ACRP-CP EXAM CONTENT OUTLINE
STUDY GUIDE 100% VERIFIED.
ACRP-CP - ANS Certified Professional in Clinical Research
Job Analysis Study - ANS Study ensuring content validity of exam
Content Areas - ANS Six main areas in ACRP-CP exam
Ethical Considerations - ANS Involves participant safety and ethics
Investigational Product Regulation - ANS Regulatory aspects of research products
Clinical Trial Operations - ANS Guidelines for Good Clinical Practices (GCPs)
Study and Site Management - ANS Tasks related to managing research studies
Scientific Concepts - ANS Understanding research design and concepts
Data Management - ANS Handling and organizing research data
1 @COPYRIGHT 2025/2026 ALLRIGHTS RESERVED.
, ACRP-CP DCO - ANS Detailed Content Outline for ACRP-CP Exam
Clinical Equipoise - ANS Balancing benefits and risks in research
Therapeutic Misconception - ANS Misunderstanding research goals as treatment
Informed Consent Form - ANS Document detailing study risks and procedures
Medical Care Continuity - ANS Ensuring study subjects receive consistent care
Investigator Brochure - ANS Details safety and therapeutic effects of investigational
product/device
Ethical Issues - ANS Identify and address past and potential ethical concerns in study conduct
Human Subject Protections - ANS Requirements for safeguarding human subjects in research
Adverse Events (AEs) - ANS Different types, identification, and reporting process for clinical
trials
Vulnerable Populations - ANS Groups needing additional safeguards in research
Conflicts of Interest - ANS Evaluate and manage potential biases in research
Risk Management Strategies - ANS Methods to mitigate risks in clinical trials
2 @COPYRIGHT 2025/2026 ALLRIGHTS RESERVED.
STUDY GUIDE 100% VERIFIED.
ACRP-CP - ANS Certified Professional in Clinical Research
Job Analysis Study - ANS Study ensuring content validity of exam
Content Areas - ANS Six main areas in ACRP-CP exam
Ethical Considerations - ANS Involves participant safety and ethics
Investigational Product Regulation - ANS Regulatory aspects of research products
Clinical Trial Operations - ANS Guidelines for Good Clinical Practices (GCPs)
Study and Site Management - ANS Tasks related to managing research studies
Scientific Concepts - ANS Understanding research design and concepts
Data Management - ANS Handling and organizing research data
1 @COPYRIGHT 2025/2026 ALLRIGHTS RESERVED.
, ACRP-CP DCO - ANS Detailed Content Outline for ACRP-CP Exam
Clinical Equipoise - ANS Balancing benefits and risks in research
Therapeutic Misconception - ANS Misunderstanding research goals as treatment
Informed Consent Form - ANS Document detailing study risks and procedures
Medical Care Continuity - ANS Ensuring study subjects receive consistent care
Investigator Brochure - ANS Details safety and therapeutic effects of investigational
product/device
Ethical Issues - ANS Identify and address past and potential ethical concerns in study conduct
Human Subject Protections - ANS Requirements for safeguarding human subjects in research
Adverse Events (AEs) - ANS Different types, identification, and reporting process for clinical
trials
Vulnerable Populations - ANS Groups needing additional safeguards in research
Conflicts of Interest - ANS Evaluate and manage potential biases in research
Risk Management Strategies - ANS Methods to mitigate risks in clinical trials
2 @COPYRIGHT 2025/2026 ALLRIGHTS RESERVED.
