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ACRP CP CERTIFICATION EXAM WITH ACTUAL QUESTIONS AND CORRECTLY WELL DEFINED ANSWERS LATEST 2024 – 2025 ALREADY GRADED A+ $16.99
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ACRP CP CERTIFICATION EXAM WITH ACTUAL QUESTIONS AND CORRECTLY WELL DEFINED ANSWERS LATEST 2024 – 2025 ALREADY GRADED A+

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ACRP CP CERTIFICATION EXAM WITH ACTUAL QUESTIONS AND CORRECTLY WELL DEFINED ANSWERS LATEST 2024 – 2025 ALREADY GRADED A+

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  • November 21, 2024
  • 36
  • 2024/2025
  • Exam (elaborations)
  • Questions & answers

Subjects

  • acrp cp certification
  • acrp cp
  • acrp cp certification exam with actual questions
  • acrp cp certification exam with actual
  • acrp cp certification exam

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  • ACRP CP
  • ACRP CP

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ACRP CP CERTIFICATION EXAM WITH
ACTUAL QUESTIONS AND CORRECTLY
WELL DEFINED ANSWERS LATEST 2024 –
2025 ALREADY GRADED A+




Incapacitated subjects can provide consent as soon as capacity is regained (T/F) -
ANSWERS-True



Who should send Annual Progress Reports to the IRB/IEC - ANSWERS-The
Investigator



The investigator is required to share names of subjects with the IRB/IEC (T/F) -
ANSWERS-False



CRAs(monitors) cannot review source documents of subjects who have
withdrawn consent. Even if the source document predates their consent
withdrawal(T/F) - ANSWERS-True



When should research studies involving human subjects be registered in a publicly
accessible database - ANSWERS-before recruiting the first subject

,Any changes to safety language in an IB should be submitted to the IRB/IEC (T/F) -
ANSWERS-True



All SAE's must be life-threatening to be considered an SAE opposed to AE (T/F) -
ANSWERS-True



After completion of a study: where should the final trial close-out monitoring
report prepared by the CRA be filed? - ANSWERS-in the Sponsor's files



During a multi-site clinical study: Whose responsibility is it to report subject
recruitment rate? - ANSWERS-CRA (Monitor)



A research subject's responsibilities for study participation should be described in
the - ANSWERS-ICF



What document would an investigator reference to learn more about the
previous clinical and nonclinical results of studies of the IP? - ANSWERS-
Investigators brochure



During a multi site clinical study: whose responsibility is it to report subject
recruitment rate? - ANSWERS-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 - ANSWERS-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... - ANSWERS-A
signed clinical trial agreement between the site and sponsor is in place.



What would be the first priority for an investigator when a subject wishes to
withdraw prematurely from the trial? - ANSWERS-Try 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 - ANSWERS-Validation

Accuracy

Reliability

Completeness



Part of a sponsor's responsibility pertaining to electronic trial data handling is to -
ANSWERS-maintain an audit trail, data trail, and edit trail.

, 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? - ANSWERS-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? - ANSWERS-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? - ANSWERS-Confirm dates of initial receipt of the sponsor protocol and the
IRB submission dates.



In a multi arm: randomized clinical trial: one arm of the protocol was terminated
due to an increased risk of cancer in subjects. Who is responsible for providing a
written report to the IRB? - ANSWERS-PI



Which of the following required elements should be included in a clinical trial
protocol? - ANSWERS-Subject inclusion and exclusion criteria



Prior to archiving a study: documentation of IP destruction at the site should be
filed in the study files of the - ANSWERS-PI and Sponsor

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