1/24/25, 8:01 P ACRP CP CERTIFICATION EXAM 2025 | QUESTIONS AND CORRECT ANSWERS | GRADED A+ | VERIFIED ANSWERS |
ACRP CP CERTIFICATION EXAM 2025 |
QUESTIONS AND CORRECT ANSWERS | GRADED
A+ | VERIFIED ANSWERS | LATEST VERSION
Terms in this set (216)
What would be the first pri Try to obtain the subject's reason for withdrawal.
ority for an investigator whe
n a subject wishes to withdr
aw prematurely
from the trial?
CRO recently switched f Validation
rom paper CRF to an ED Accurac
C system. The EDC syst y Reliabili
em must conform to the e ty
stablished Completeness
requirements for
Part of a sponsor's maintain an audit trail, data trail, and edit trail.
responsibility pertaining to el
ectronic trial data
handling is to
A research subject's ICF
responsibilities for study part
icipation should be describ
ed in the
https://quizlet.com/996944680/acrp-cp-certification-exam-2025-questions-and-correct-answers-graded-a-verified-answers-latest-version-study-this-on… 1/26
,1/24/25, 8:01 P ACRP CP CERTIFICATION EXAM 2025 | QUESTIONS AND CORRECT ANSWERS | GRADED A+ | VERIFIED ANSWERS |
What document would an Investigators brochure
investigator reference t
o learn more about the
previous clinical and nonclini
cal results of
studies of the IP?
During a multi site clinical st The CRA
udy: whose
responsibility is it to report
subject recruitment rate?
An unconscious adult Obtain consent from the subject for the study
subject was enrolled in a stu
dy after obtaining
consent from an LAR: and pr
otocol therapy was
initiated. The subject sho
wed significant
improvement in his clinical co
ndition: and regained cons
ciousness. The
Investigator should inform th
e subject about the
study and
A site is in the start up ph A signed clinical trial agreement between the site and s
ase of an industry ponsor is in place.
sponsored phase 3 trial:
and has received IRB
approval. The site can b
egin enrolling subjects af
ter...
https://quizlet.com/996944680/acrp-cp-certification-exam-2025-questions-and-correct-answers-graded-a-verified-answers-latest-version-study-this-on… 2/26
, 1/24/25, 8:01 P ACRP CP CERTIFICATION EXAM 2025 | QUESTIONS AND CORRECT ANSWERS | GRADED A+ | VERIFIED ANSWERS |
A site is screening A research assistant who is certified to administer the psychom
potential subjects for a s etric test
tudy looking at mild cogn
itive impairment. One of th
e inclusion criteria is a sco
re of 25 or less on a psyc
hometric test: a
research specific tool w
hich measures cognitive a
bility. Which of the
following individuals can
administer the psychom
etric test to the
potential subjects?
A research study: in which th Wording indicating that there is no expected benefit sh
ere is no intended ould be included
clinical benefit to the sub
ject: is being submitted to t
he IRB. WhatGbenefit info
rmation should be
included in the ICF?
A CRA notices during an Confirm dates of initial receipt of the sponsor protoco
onsite visit that the date l and the IRB submission dates.
on IRB approval letter for
a protocol is prior to the
effective date indicate
d on the cover page of t
he protocol and the
signatures of the
investigator and sponsor.
WhatGshould theGCRAGd
o FIRST?
https://quizlet.com/996944680/acrp-cp-certification-exam-2025-questions-and-correct-answers-graded-a-verified-answers-latest-version-study-this-on… 3/26
ACRP CP CERTIFICATION EXAM 2025 |
QUESTIONS AND CORRECT ANSWERS | GRADED
A+ | VERIFIED ANSWERS | LATEST VERSION
Terms in this set (216)
What would be the first pri Try to obtain the subject's reason for withdrawal.
ority for an investigator whe
n a subject wishes to withdr
aw prematurely
from the trial?
CRO recently switched f Validation
rom paper CRF to an ED Accurac
C system. The EDC syst y Reliabili
em must conform to the e ty
stablished Completeness
requirements for
Part of a sponsor's maintain an audit trail, data trail, and edit trail.
responsibility pertaining to el
ectronic trial data
handling is to
A research subject's ICF
responsibilities for study part
icipation should be describ
ed in the
https://quizlet.com/996944680/acrp-cp-certification-exam-2025-questions-and-correct-answers-graded-a-verified-answers-latest-version-study-this-on… 1/26
,1/24/25, 8:01 P ACRP CP CERTIFICATION EXAM 2025 | QUESTIONS AND CORRECT ANSWERS | GRADED A+ | VERIFIED ANSWERS |
What document would an Investigators brochure
investigator reference t
o learn more about the
previous clinical and nonclini
cal results of
studies of the IP?
During a multi site clinical st The CRA
udy: whose
responsibility is it to report
subject recruitment rate?
An unconscious adult Obtain consent from the subject for the study
subject was enrolled in a stu
dy after obtaining
consent from an LAR: and pr
otocol therapy was
initiated. The subject sho
wed significant
improvement in his clinical co
ndition: and regained cons
ciousness. The
Investigator should inform th
e subject about the
study and
A site is in the start up ph A signed clinical trial agreement between the site and s
ase of an industry ponsor is in place.
sponsored phase 3 trial:
and has received IRB
approval. The site can b
egin enrolling subjects af
ter...
https://quizlet.com/996944680/acrp-cp-certification-exam-2025-questions-and-correct-answers-graded-a-verified-answers-latest-version-study-this-on… 2/26
, 1/24/25, 8:01 P ACRP CP CERTIFICATION EXAM 2025 | QUESTIONS AND CORRECT ANSWERS | GRADED A+ | VERIFIED ANSWERS |
A site is screening A research assistant who is certified to administer the psychom
potential subjects for a s etric test
tudy looking at mild cogn
itive impairment. One of th
e inclusion criteria is a sco
re of 25 or less on a psyc
hometric test: a
research specific tool w
hich measures cognitive a
bility. Which of the
following individuals can
administer the psychom
etric test to the
potential subjects?
A research study: in which th Wording indicating that there is no expected benefit sh
ere is no intended ould be included
clinical benefit to the sub
ject: is being submitted to t
he IRB. WhatGbenefit info
rmation should be
included in the ICF?
A CRA notices during an Confirm dates of initial receipt of the sponsor protoco
onsite visit that the date l and the IRB submission dates.
on IRB approval letter for
a protocol is prior to the
effective date indicate
d on the cover page of t
he protocol and the
signatures of the
investigator and sponsor.
WhatGshould theGCRAGd
o FIRST?
https://quizlet.com/996944680/acrp-cp-certification-exam-2025-questions-and-correct-answers-graded-a-verified-answers-latest-version-study-this-on… 3/26
