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ACRP ACRP-CP Exam Overview:
| Certification Vendor: | Association of Clinical Research Professionals (ACRP) |
| Exam Name: | ACRP Certified Professional Exam |
| Exam Number: | ACRP-CP |
| Certificate Validity Period: | 2 years |
| Real Exam Qty: | 125 |
| Exam Duration: | 180 minutes |
| Available Languages: | English |
| Exam Format: | Multiple Choice |
| Related Certifications: | CCRA CCRC CPI ACRP-MDP ACRP-PM |
| Passing Score: | 600/800 |
| Exam Price: | $550 USD |
| Sample Questions: | ACRP ACRP-CP Sample Questions |
| Exam Way: | Online remote proctored exam or in-person test center delivery |
| Pre Condition: | Candidates must have 3000 hours of verifiable clinical research work experience, or qualify for a partial experience waiver through eligible education or existing ACRP certification. |
| Official Syllabus URL: | https://acrpnet.org/certification/acrp-cp-certification |
ACRP ACRP-CP Exam Syllabus Topics:
| Section | Objectives |
|---|---|
| Topic 1: Ethical and Participant Safety Considerations | - Human subject protection
|
| Topic 2: Quality Management | - Risk management
|
| Topic 3: Professional Responsibilities | - Communication and collaboration
|
| Topic 4: Clinical Trial Operations | - Study conduct
|
| Topic 5: Data Management and Documentation | - Clinical trial documentation
|
ACRP Certified Professional Sample Questions:
1. After the completion or termination of a clinical trial, who should store the enrollment log?
A) Regulatory authority
B) Sponsor
C) PI
D) CRO
2. Prior to initiation of a clinical trial, review by an IRB/IEC is required for which of the following documents?
A) Protocol, IB, and information about payments and compensation available to subjects
B) IB, site coordinator CVs, and information about payments and compensation available to subjects
C) Protocol, informed consent, and clinical trial agreement
D) Protocol, site coordinator CVs, and clinical trial agreement
3. A new device trial is being considered. Before committing to participate in the trial, what is the MOST important item the PI needs to evaluate?
A) Availability of qualified staff to conduct the trial
B) Location of stored trial records
C) Length of time to receive the approved trial device
D) Information to be included in the advertising flyer
4. Who is responsible for defining, establishing, and allocating all trial-related duties and functions prior to initiating a trial?
A) Investigator
B) IRB/IEC
C) Sponsor
D) CRO
5. Per the protocol, participants' blood creatinine level must be no greater than 2.5 times the upper limit of normal (0.7-1.2 mg/dL). What is the maximum creatinine level the participant can have and be eligible for the trial?
A) 3.6 mg/dL
B) 2.6 mg/dL
C) 3.0 mg/dL
D) 1.8 mg/dL
Solutions:
| Question # 1 Answer: C | Question # 2 Answer: A | Question # 3 Answer: A | Question # 4 Answer: C | Question # 5 Answer: C |
By Susie
