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2024 update |ACRP-CP Certification Exam| most recent |COMPLETE MOST TESTED QUESTIONS AND VERIFIED ANSWERS | (100% correct solutions)|GET IT A+ RIGHT!!$15.99
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10/30/24, 9:27 PM 2024 update |ACRP-CP Certification Exam|2024-2025 most recent |COMPLETE MOST TESTED QUESTIONS AND VERIFI…
2024 update |ACRP-CP Certification
Exam|2024-2025 most recent |COMPLETE
MOST TESTED QUESTIONS AND VERIFIED
ANSWERS | (100% correct solutions)|GET IT A+
RIGHT!!
Terms in this set (216)
What would be the first Try to obtain the subject's reason for withdrawal.
priority for an
investigator when a
subject wishes to
withdraw prematurely
from the trial?
CRO recently switched Validation
from paper CRF to an Accuracy
EDC system. The EDC Reliability
system must conform to Completeness
the established
requirements for
Part of a sponsor's maintain an audit trail, data trail, and edit trail.
responsibility pertaining
to electronic trial data
handling is to
A research subject's ICF
responsibilities for study
participation should be
described in the
,10/30/24, 9:27 PM 2024 update |ACRP-CP Certification Exam|2024-2025 most recent |COMPLETE MOST TESTED QUESTIONS AND VERIFI…
What document would Investigators brochure
an investigator reference
to learn more about the
previous clinical and
nonclinical results of
studies of the IP?
During a multi site clinical The CRA
study: 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
study after obtaining
consent from an LAR:
and protocol therapy was
initiated. The subject
showed significant
improvement in his
clinical condition: and
regained consciousness.
The Investigator should
inform the subject about
the study and
A site is in the start up A signed clinical trial agreement between the site
phase of an industry and sponsor is in place.
sponsored phase 3 trial:
and has received IRB
approval. The site can
begin enrolling subjects
after...
, 10/30/24, 9:27 PM 2024 update |ACRP-CP Certification Exam|2024-2025 most recent |COMPLETE MOST TESTED QUESTIONS AND VERIFI…
A site is screening A research assistant who is certified to administer
potential subjects for a the psychometric test
study looking at mild
cognitive impairment.
One of the inclusion
criteria is a score of 25 or
less on a psychometric
test: a research specific
tool which measures
cognitive ability. Which of
the following individuals
can administer the
psychometric test to the
potential subjects?
A research study: in Wording indicating that there is no expected benefit
which there is no should be included
intended clinical benefit
to the subject: is being
submitted to the IRB.
What benefit information
should be included in the
ICF?
A CRA notices during an Confirm dates of initial receipt of the sponsor
onsite visit that the date protocol and the IRB submission dates.
on IRB approval letter for
a protocol is prior to the
effective date indicated
on the cover page of the
protocol and the
signatures of the
investigator and sponsor.
What should the CRA do
FIRST?
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