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ACRP PRACTICE EXAM 2022 QUESTIONS AND ANSWERS

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[COMPANY NAME] [Company address] ACRP PRACTICE EXAM 2022 QUESTIONS AND ANSWERSA subject is issued 120 tablets and is instructed to take 2 tablets 4 times a day. He returns 88 tablets on the morning of day 9 fasting for laboratory tests. What percent compliant is he? - ANSWER 50% To be eligibl...

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  • October 20, 2022
  • 9
  • 2022/2023
  • Exam (elaborations)
  • Questions & answers
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ACRP PRACTICE EXAM
2022 QUESTIONS AND
ANSWERS




marshiks12@gmail.com
[COMPANY NAME] [Company address]

, ACRP Practice Exam 2022 Questions
and Answers
A subject is issued 120 tablets and is instructed to take 2 tablets 4 times a day. He
returns 88 tablets on the morning of day 9 fasting for laboratory tests. What percent
compliant is he? - ANSWER 50%

To be eligible for a trial, the subjects must have liver function tests no greater than two
times the upper limit normal and rental function tests no greater than three times the
upper limit normal. All of the following are normal ranges for the trial:
AST 5-65
ALT 5-35
BUN 4-25
Creat 0.5-1.2
Amylase 56-190
Lipase 4-24
ALK Phos 0-110 - ANSWER AST 130; ALT; 70; BUN 50; Create 2.4

A subject presents at a site with her husband after pre-qualifying on a phone screen.
She states that she is legally blind and cannot read the ICF. A Braille ICF is not
available. This subject is able to sign her name if her hand is guided to the signature
line. Which of the following is the BEST course of action to obtain legal consent from the
subject? - ANSWER The subject and an impartial witness can sign the ICF after it is
read to them and she verbally states her understanding.

Which of the following is MOST useful for scheduling trial procedures? - ANSWER trial
schedule of events

A subject is participating in a clinical trial where only the pharmacist and sponsor knows
the identity of the IP. The pharmacist has no contact with the trial subject and the clinical
team. Which of the following BEST describes this trial type? - ANSWER double blind

A site has not received IRB/IEC approval for a protocol submission. The PI instructs the
CRC employed by the clinic to begin scheduling subjects for screening appointments.
Which of the following is the BEST course of action for the CRC to take? - ANSWER
Review the research database and collate a list of potential subjects

The trough blood level for once daily drug should be drawn how long after the last
dose? - ANSWER 24 hours

A potential subject for a trial has been mailed an ICF prior to his screening visit. When
the subject arrives at the research dept for his screening visit, he states he read the ICF
and is ready to do the trial. He does not have a copy of the ICF that was mailed to his

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