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ACRP CP FINAL EXAM AND PRACTICE EXAM QUESTIONS ACTUAL EXAM COMPLETE ACCURATE EXAM QUESTIONS WITH DETAILED VERIFIED ANSWERS (100% CORRECT ANSWERS) /ALREADY GRADED A+ $18.19
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ACRP CP FINAL EXAM AND PRACTICE EXAM QUESTIONS ACTUAL EXAM COMPLETE ACCURATE EXAM QUESTIONS WITH DETAILED VERIFIED ANSWERS (100% CORRECT ANSWERS) /ALREADY GRADED A+

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ACRP CP FINAL EXAM AND PRACTICE
EXAM QUESTIONS 2024-2025 ACTUAL
EXAM COMPLETE ACCURATE EXAM
QUESTIONS WITH DETAILED VERIFIED
ANSWERS (100% CORRECT ANSWERS)
/ALREADY GRADED A+




What information must be provided to subjects
regarding their participation, according to 46/116(b)?
Participation is voluntary and they may discontinue
at any time without penalty or loss of benefits


What must be included in the informed consent
process when research involves more than minimal
risk?
An explanation of whether compensation and
medical treatments are available if injury occurs


For research involving identifiable private
information or biospecimens, what must be included
in the informed consent?

,A statement about whether identifiers might be
removed and whether the information could be used
for future research without additional consent


According to 46/116(b), informed consent must
include a statement regarding:
The expected duration of the subject's participation


If alternative procedures or courses of treatment
are available, what must be included in the informed
consent?
A disclosure of appropriate alternatives that might
be advantageous to the subject


Which statement about participation must be
included in the informed consent?
Subjects may discontinue participation at any time
without penalty or loss of benefits


According to 46/116(b), what must be included in
informed consent regarding the potential benefits of
the research?

,A description of any benefits to the subjects or to
others that may reasonably be expected from the
research


According to 46/116(b), informed consent must
include contact information for:
Whom to contact for answers to questions about the
research, the subject's rights, and in the event of a
research-related injury


Which of the following elements must be included in
informed consent if relevant to the research,
according to 46/116(b)?
Any additional costs to the subject that may result
from participation in the research**


What must be included in informed consent when
research involves risks to an embryo or fetus?
A statement that the procedure may involve
unforeseeable risks to the subject or to the embryo
or fetus if the subject is or may become pregnant

, In the event of new findings during the course of the
research, what should be communicated to the
subjects?
Significant new findings that may affect the subject's
willingness to continue participation should be
provided to the subject


According to 46/116(b), under what circumstances
can a subject's participation be terminated without
their consent?
If the investigator determines it is necessary based
on anticipated circumstances


For research subject to HHS regulation at 45 CFR 46,
what must be included in the consent form regarding
biospecimens?
A statement regarding whether biospecimens may
be used for commercial profit and whether the
subject will or will not share in this profit


What must the informed consent include if the
research might include whole genome sequencing of
biospecimens?
A guarantee that only partial genome sequencing
will be conducted

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