ACRP-CP Dumps

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Overview of ACRP Certification

ACRP certification validates clinical research professionals' competence and promotes continuous learning. Earning the ACRP certification will make the managers:

•Reduce risk with third-party validation of team competence.

•Enhance clinical trial operations via better inspections, patient enrollment, and compliance.

•Support growth and retention by providing professional development pathways.

•Show advanced team knowledge to differentiate study teams.

•Save money through volume-based pricing.

Currently, there are six ACRP certification programs below:

•ACRP Certified Professional (ACRP-CP)

•Certified Clinical Research Associate (CCRA)

•Certified Clinical Research Coordinator (CCRC)

•Certified Principal Investigator (CPI)

•ACRP Medical Device Professional (ACRP-MDP)

•ACRP Project Manager (ACRP-PM)

Among these programs, the ACRP-CP certification recognizes clinical research professionals across all roles on clinical study teams. It demonstrates that a professional has proficiency in key knowledge and skills.

Eligibility Paths to ACRP-CP Exam

The ACRP Certified Professional (ACRP-CP) certification is ideal for professionals who want to validate their expertise across multiple roles in clinical research. There are two pathways to achieve the ACRP-CP certification.

Pathway 1: Work Experience

You qualify if you have:

•3,000 hours of verifiable work experience in clinical research.

•This must be:

    º Related to human subject research

    º Paid and employer-verified

    º Within the last 10 years

•Internships or unpaid work do not count.

Pathway 2: Work Experience + Waiver

•You may be eligible with only 1,500 hours if:

    º You hold another active ACRP certification, or you have completed a clinical research education program

•The education program must be:

    º Aligned with ACRP’s Exam Content Outline (ECO)

    º Third-party accredited

    º Equivalent in learning to 1,500 hours of work experience

ACRP-CP Exam Content

The ACRP Certified Professional (ACRP-CP) consists of 125 multiple-choice questions that must be answered within 180 minutes, which details the knowledge domains and topics covered on the exam.

1. Scientific Concepts and Research Ethics (15 questions)

Focuses on foundational ethical principles and subject protection:

•Clinical equipoise, standard of care, risks vs. benefits

•Informed consent, confidentiality, and vulnerable populations

•Protocol violations, recruitment, and safety monitoring

•Fraud, misconduct, conflicts of interest

2. Clinical Research Standards and Guidelines (17 questions)

Covers compliance frameworks and regulatory processes:

•ICH-GCP, IRB/IEC roles, regulatory reporting

•Audit & inspection processes, protocol amendments

•Safety evaluations (e.g., DSMB review)

3. Clinical Trial Operations (GCPs) (25 questions)

Hands-on trial operations:

•Study conduct, documentation, and management

•Staff qualifications and delegation

•Investigational product handling

•AE/SAE reporting, monitoring, GCP deviations

4. Study and Site Management (21 questions)

Operational management at clinical sites:

•PI/CRO/sponsor responsibilities

•Site selection and initiation

•Contractual agreements, equipment, and compliance

•Document retention, trial master file

5. Research Design and Data Management (19 questions)

Data and protocol-related topics:

•Trial design (e.g., double-blind, crossover)

•Protocol components, IB instructions

•Biostatistics basics, endpoint development

•ALCOA-C principles (data documentation standards)

•EDC, data privacy, audit trails

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