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ACRP Certified Professional Sample Questions:

1. Which of the following reports should be retained in participant charts?

A) Lab reports
B) Safety reports
C) IRB/IEC progress reports
D) DSMB/IDMC reports

2. The objective of a randomized clinical trial is to look at whether an IP is effective in preventing recurrence of a disease. What would be a possible primary endpoint of the trial?

A) Impact of an approved vaccine against the disease
B) Time to occurrence of symptoms of the disease
C) Use of concomitant medications to treat the symptoms
D) Occurrence of known side effects of the IP

3. Who determines what criteria and procedures should be followed if a subject discontinues/withdraws their consent?

A) Sponsor
B) Subject
C) PI
D) CRO

4. The process of ensuring and documenting that an electronic data processing system conforms to the sponsor's established requirements for completeness, accuracy, reliability, and consistent intended performance is called:

A) Quality Control
B) Programming
C) Validation
D) Quality Assurance

5. The coding system for a double-blind clinical trial is accessible by the:

A) Sponsor
B) Regulatory authority
C) PI
D) IRB/IEC

Solutions: