ACRP-CP CERTIFICATION EXAM 2026|LATEST ACTUAL EXAM WITH 100% VERIFIED QUESTIONS AND CORRECT ANSWERS|EXCELLENT SCORES

ACRP-CP CERTIFICATION EXAM 2026|LATEST ACTUAL EXAM WITH 100% VERIFIED QUESTIONS AND CORRECT ANSWERS|EXCELLENT SCORES
ACRP-CP CERTIFICATION EXAM
2026|LATEST ACTUAL EXAM
WITH 100% VERIFIED
QUESTIONS AND CORRECT
ANSWERS|EXCELLENT SCORES
What would be the first priority for an investigator when a subject
wishes to withdraw prematurely from the trial? - CORRECT-ANSWERTry to obtain the subject's reason for withdrawal.
CRO recently switched from paper CRF to an EDC system. The EDC
system must conform to the established requirements for - CORRECTANSWER-Validation
Accuracy
Reliability
Completeness
Part of a sponsor's responsibility pertaining to electronic trial data
handling is to - CORRECT-ANSWER-maintain an audit trail, data trail,
and edit trail.
A research subject's responsibilities for study participation should be
described in the - CORRECT-ANSWER-ICF
What document would an investigator reference to learn more about
the previous clinical and nonclinical results of studies of the IP? -
CORRECT-ANSWER-Investigators brochure
During a multi site clinical study: whose responsibility is it to report
subject recruitment rate? - CORRECT-ANSWER-The CRA
An unconscious adult 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 - CORRECT-ANSWER-Obtain consent from the subject for the
study
A site is in the start up phase of an industry sponsored phase 3 trial:
and has received IRB approval. The site can begin enrolling subjects
after... - CORRECT-ANSWER-A signed clinical trial agreement between
the site and sponsor is in place.
A site is screening potential subjects for a 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? - CORRECT-ANSWER-A
research assistant who is certified to administer the psychometric test
A research study: in which there is no intended clinical benefit to the
subject: is being submitted to the IRB. What benefit information should
be included in the ICF? - CORRECT-ANSWER-Wording indicating that
there is no expected benefit should be included
A CRA notices during an onsite visit that the date 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? - CORRECT-ANSWER-Confirm dates of
initial receipt of the sponsor protocol and the IRB submission dates.

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