ACRP CP CERTIFICATION EXAM 2025-2026 ACTUAL EXAM
COMPLETE ACCURATE EXAM QUESTIONS WITH DETAILED
VERIFIED ANSWERS (100% CORRECT ANSWERS
A blood sample collection is required to screen for bloodborne
pathogens before subject could be enrolled in a study. Where will
subjects find information of the procedures and any foreseeable risks or
inconveniences? - correct answer- ICF
A blood sample collection is required to screen for bloodborne
pathogens before subject could be enrolled in a study. Where will
subjects find information of the procedures and any foreseeable risks or
inconveniences? - correct answer- ICF
A Clinical Research Coordinator (CRC) adjusted the dose of the
Investigation Product (IP) for a subject as the subject was suffering from
Adverse Events (AEs) like headaches and vomiting. When is a CRC
allowed to do this task? - correct answer- Only when the CRC is a
qualified physician and has been delegated this responsibility by the PI
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.
,A CRA notices during an onsite visit that the date on IRB/IEC 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/IEC submission dates.
A CRO recently switched from paper CRF to an EDC system. The EDC
system must conform to the established requirements for - correct
answer- validation, accuracy, reliability, and completeness.
A medical student is approached by a faculty member for possible
participation in a cricothyroidotomy simulation research study. Which of
the following increases risk to the subject? - correct answer-
Consenting in the presence of figure of authority
A medical student is approaches by a faculty member for possible
participation in a cricothyroidotomy simulation research study. Which of
the following increases risk to the study? - correct answer-
Consenting in the presence of figure of authority
A new study is investigating a new IND "glue" that can be used to hold
skin cuts together and decrease the chance of scaring. You know
children should be included because ICH E8 considers them a special
population. In designing the protocol you should expect to - correct
answer- Include children in the general plan from the beginning
,A non-English speaking subject has responded to a recruitment ad to
participate in a trial for treatment of her diabetes. She arrives at the site
with her daughter who is fluent in English. The informed consent forms
are only available in English. What actions are compliant with GCP? -
correct answer- Call the sponsor to request a translation of the
informed consent
A randomised controlled trial ( RCT ) that lets you carry out 2 or more
treatment comparisons at the same time. while multiple factors are
manipulated - correct answer- Factorial Study
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 research study: in which there is no intended clinical benefit to the
subject: is being submitted to the IRB/IEC. What benefit information
should be included in the ICF? - correct answer- Wording indicating
that there is no expected benefit should be included.
A research subject's responsibilities for study participation should be
described in the - correct answer- ICF
A research subject's responsibilities for study participation should be
described in the - correct answer- ICF
, 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 in the start-up phase of an industry-sponsored phase 3 trial: and
has received IRB/IEC 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 in the start-up phase of an industry-sponsored phase 3 trial: and
has received IRB/IEC approval. When can the site begin enrolling
subjects? - correct answer- after 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 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
COMPLETE ACCURATE EXAM QUESTIONS WITH DETAILED
VERIFIED ANSWERS (100% CORRECT ANSWERS
A blood sample collection is required to screen for bloodborne
pathogens before subject could be enrolled in a study. Where will
subjects find information of the procedures and any foreseeable risks or
inconveniences? - correct answer- ICF
A blood sample collection is required to screen for bloodborne
pathogens before subject could be enrolled in a study. Where will
subjects find information of the procedures and any foreseeable risks or
inconveniences? - correct answer- ICF
A Clinical Research Coordinator (CRC) adjusted the dose of the
Investigation Product (IP) for a subject as the subject was suffering from
Adverse Events (AEs) like headaches and vomiting. When is a CRC
allowed to do this task? - correct answer- Only when the CRC is a
qualified physician and has been delegated this responsibility by the PI
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.
,A CRA notices during an onsite visit that the date on IRB/IEC 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/IEC submission dates.
A CRO recently switched from paper CRF to an EDC system. The EDC
system must conform to the established requirements for - correct
answer- validation, accuracy, reliability, and completeness.
A medical student is approached by a faculty member for possible
participation in a cricothyroidotomy simulation research study. Which of
the following increases risk to the subject? - correct answer-
Consenting in the presence of figure of authority
A medical student is approaches by a faculty member for possible
participation in a cricothyroidotomy simulation research study. Which of
the following increases risk to the study? - correct answer-
Consenting in the presence of figure of authority
A new study is investigating a new IND "glue" that can be used to hold
skin cuts together and decrease the chance of scaring. You know
children should be included because ICH E8 considers them a special
population. In designing the protocol you should expect to - correct
answer- Include children in the general plan from the beginning
,A non-English speaking subject has responded to a recruitment ad to
participate in a trial for treatment of her diabetes. She arrives at the site
with her daughter who is fluent in English. The informed consent forms
are only available in English. What actions are compliant with GCP? -
correct answer- Call the sponsor to request a translation of the
informed consent
A randomised controlled trial ( RCT ) that lets you carry out 2 or more
treatment comparisons at the same time. while multiple factors are
manipulated - correct answer- Factorial Study
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 research study: in which there is no intended clinical benefit to the
subject: is being submitted to the IRB/IEC. What benefit information
should be included in the ICF? - correct answer- Wording indicating
that there is no expected benefit should be included.
A research subject's responsibilities for study participation should be
described in the - correct answer- ICF
A research subject's responsibilities for study participation should be
described in the - correct answer- ICF
, 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 in the start-up phase of an industry-sponsored phase 3 trial: and
has received IRB/IEC 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 in the start-up phase of an industry-sponsored phase 3 trial: and
has received IRB/IEC approval. When can the site begin enrolling
subjects? - correct answer- after 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 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
