ACRP-CP CERTIFICATION EXAM |COMPLETE QUESTIONS WITH
EXPERT SOLUTIONS | 2026 LATEST UPDATED | GET A+
What would be the first priority for an investigator when a subject wishes to withdraw
prematurely from the trial? - (answer)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 - (answer)Validation
Accuracy
Reliability
Completeness
Part of a sponsor's responsibility pertaining to electronic trial data handling is to -
(answer)maintain an audit trail, data trail, and edit trail.
A research subject's responsibilities for study participation should be described in the -
(answer)ICF
What document would an investigator reference to learn more about the previous clinical and
nonclinical results of studies of the IP? - (answer)Investigators brochure
During a multi site clinical study: whose responsibility is it to report subject recruitment rate? -
(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 - (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... - (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? - (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? - (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? - (answer)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?
- (answer)PI
Which of the following required elements should be included in a clinical trial protocol? -
(answer)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 - (answer)PI and Sponsor
During a monitoring visit: what records would a CRA reference to verify a subject's compliance
to the study visit schedule and assessments? - (answer)Electronic medical record
,When considering participation in a study: the investigator should determine if he... -
(answer)Sees enough patients who would qualify for the study
New safety information has become available from the Sponsor about the IP being used in a
clinical trial. The investigator must - (answer)Submit a revised ICF to the IRB noting the new
safety information
Per ICH: an IRB must keep correspondence for at least how long after the completion of a
clinical trial? - (answer)3 Years
When would an impartial witness be needed during the consent process for an illiterate subject? -
(answer)To observe the consent process
A study which seeks to determine the ideal dose and regimen of a new IP to treat hypothyroidism
is considered to be - (answer)Phase II
After completion of a study: the final trial close out monitoring report prepared by the CRA
should be filed in which of the following stakeholder files? - (answer)The sponsors files
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? - (answer)ICF
When should a research study involving human subjects be registered in a publicly accessible
database? - (answer)Before recruiting the first subject
In the case of an incapacitated subject: who should receive a copy of the signed and dated ICF? -
(answer)The subjects legally acceptable representative
, 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?
- (answer)Consenting in the presence of figure of authority
The clinical trial phase that focuses on safety and human pharmacology in healthy volunteers -
(answer)Phase I
Who is ultimately responsible for all aspects of the research conducted at a site? -
(answer)Principal investigator
An international quality standard that is provided by ICH E6(R2) describing safety: accuracy of
trials and credibility of data - (answer)GCP
What event resulted in the Nuremburg Cod of 1949 - (answer)Nazi Medical Experiments
Prior to archiving a study: documentation of IP destruction at the site should be filed in the study
files of the - (answer)PI and Sponsor
In the case of an incapacitated subject: who should receive a copy of the signed and dated ICF? -
(answer)The subject's legally acceptable representative
Which of the following required elements should be included in a clinical trial protocol? -
(answer)The subject inclusion and exclusion criteria
During a multi-site clinical study: whose responsibility is it to report subject recruitment rate? -
(answer)The CRA
A study which seeks to determine the ideal dose and regimen of a new IP to treat hypothyroidism
is considered to be - (answer)Phase II
EXPERT SOLUTIONS | 2026 LATEST UPDATED | GET A+
What would be the first priority for an investigator when a subject wishes to withdraw
prematurely from the trial? - (answer)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 - (answer)Validation
Accuracy
Reliability
Completeness
Part of a sponsor's responsibility pertaining to electronic trial data handling is to -
(answer)maintain an audit trail, data trail, and edit trail.
A research subject's responsibilities for study participation should be described in the -
(answer)ICF
What document would an investigator reference to learn more about the previous clinical and
nonclinical results of studies of the IP? - (answer)Investigators brochure
During a multi site clinical study: whose responsibility is it to report subject recruitment rate? -
(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 - (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... - (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? - (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? - (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? - (answer)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?
- (answer)PI
Which of the following required elements should be included in a clinical trial protocol? -
(answer)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 - (answer)PI and Sponsor
During a monitoring visit: what records would a CRA reference to verify a subject's compliance
to the study visit schedule and assessments? - (answer)Electronic medical record
,When considering participation in a study: the investigator should determine if he... -
(answer)Sees enough patients who would qualify for the study
New safety information has become available from the Sponsor about the IP being used in a
clinical trial. The investigator must - (answer)Submit a revised ICF to the IRB noting the new
safety information
Per ICH: an IRB must keep correspondence for at least how long after the completion of a
clinical trial? - (answer)3 Years
When would an impartial witness be needed during the consent process for an illiterate subject? -
(answer)To observe the consent process
A study which seeks to determine the ideal dose and regimen of a new IP to treat hypothyroidism
is considered to be - (answer)Phase II
After completion of a study: the final trial close out monitoring report prepared by the CRA
should be filed in which of the following stakeholder files? - (answer)The sponsors files
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? - (answer)ICF
When should a research study involving human subjects be registered in a publicly accessible
database? - (answer)Before recruiting the first subject
In the case of an incapacitated subject: who should receive a copy of the signed and dated ICF? -
(answer)The subjects legally acceptable representative
, 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?
- (answer)Consenting in the presence of figure of authority
The clinical trial phase that focuses on safety and human pharmacology in healthy volunteers -
(answer)Phase I
Who is ultimately responsible for all aspects of the research conducted at a site? -
(answer)Principal investigator
An international quality standard that is provided by ICH E6(R2) describing safety: accuracy of
trials and credibility of data - (answer)GCP
What event resulted in the Nuremburg Cod of 1949 - (answer)Nazi Medical Experiments
Prior to archiving a study: documentation of IP destruction at the site should be filed in the study
files of the - (answer)PI and Sponsor
In the case of an incapacitated subject: who should receive a copy of the signed and dated ICF? -
(answer)The subject's legally acceptable representative
Which of the following required elements should be included in a clinical trial protocol? -
(answer)The subject inclusion and exclusion criteria
During a multi-site clinical study: whose responsibility is it to report subject recruitment rate? -
(answer)The CRA
A study which seeks to determine the ideal dose and regimen of a new IP to treat hypothyroidism
is considered to be - (answer)Phase II
