ACRP ACRP-CP Questions & Answers - in .pdf
- Total Q&A: 127
- Update: Aug 25, 2026
- Price: $59.99
- Vendor: ACRP
- Exam Code: ACRP-CP
- Exam Name: ACRP Certified Professional Exam
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- Total Q&A: 127
- Update: Aug 25, 2026
- Price: $59.99
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- Exam Code: ACRP-CP
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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 |
| Passing Score: | 600/800 |
| Certificate Validity Period: | 2 years |
| Related Certifications: | CCRA CCRC CPI ACRP-MDP ACRP-PM |
| Exam Format: | Multiple Choice |
| Real Exam Qty: | 125 |
| Available Languages: | English |
| Exam Price: | $550 USD |
| Exam Duration: | 180 minutes |
| 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 |
|---|---|
| Ethical and Participant Safety Considerations | - Human subject protection
|
| Data Management and Documentation | - Data integrity
|
| Clinical Trial Operations | - Study start-up activities
|
| Quality Management | - Audit and inspection readiness
|
| Professional Responsibilities | - Leadership and professionalism
|
ACRP Certified Professional Sample Questions:
1. Which one of the following is a primary objective of a Phase III study of a new IP?
A) To demonstrate or confirm therapeutic benefit
B) To establish the safety profile
C) To establish dose information
D) To show superiority over another treatment
2. IP is dispensed to all subjects who:
A) Need IP for their medical condition.
B) Consented for the trial.
C) Are eligible to receive it in the trial.
D) Screened for the trial.
3. The site submitted all start-up documents for a study to the sponsor and the IRB/IEC. The site also has subjects identified for screening. What should happen FIRST?
A) Obtain IRB/IEC approval
B) Ship/receive IP
C) Verify subject eligibility
D) Schedule a site initiation visit
4. Who is responsible for submitting a protocol amendment to the IRB/IEC?
A) CRC
B) Sponsor
C) CRA
D) Investigator
5. Upon receipt of temperature-controlled IP, the study staff noticed the IP incurred a temperature excursion during transport. What should the staff do NEXT?
A) Register IP in IWRS and continue with subject allocation.
B) Quarantine IP without registering in IWRS and request replacement from sponsor.
C) Register IP in IWRS, quarantine and notify sponsor of the excursion.
D) Dispose of IP and request replacement from sponsor.
Solutions:
| Question # 1 Answer: A | Question # 2 Answer: C | Question # 3 Answer: A | Question # 4 Answer: D | Question # 5 Answer: C |
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