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: | ACRP-PM CCRC CPI CCRA ACRP-MDP |
| 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:
After the completion or termination of a clinical trial, who should store the enrollment log?
- A. Regulatory authority
- B. Sponsor
- C. PI
- D. CRO
Correct Answer: C 🗳️
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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
Correct Answer: A 🗳️
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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
Correct Answer: A 🗳️
Explanation: Only visible for BraindumpQuiz members. You can sign-up / login (it's free).
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
Correct Answer: C 🗳️
Explanation: Only visible for BraindumpQuiz members. You can sign-up / login (it's free).
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
Correct Answer: C 🗳️
Explanation: Only visible for BraindumpQuiz members. You can sign-up / login (it's free).
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