1|Page
ACRP CP CERTIFICATION EXAM LATEST 2026
ACTUAL EXAM WITH COMPLETE QUESTIONS AND
CORRECT DETAILED ANSWERS ||VERIFIED
EXAM!!!(100% VERIFIED ANSWERS) |ALREADY
GRADED A+| ||PROFESSOR VERIFIED|| ||NEWEST
EXAM!!!!!!||
In any trial, what should be the main concern of the
physician? - Answer-The welfare of the subjects
The world medical association (WMA) ethical principles for
medical research involving human subjects is called: -
Answer-The Declaration of Helsinki
The process by which a subject voluntarily confirms his or
her willingness to participate in a clinical trial is known as:
- Answer-Informed Consent of Trial Subjects
What does the IRB/IEC evaluate? - Answer-The scientific
tenability of the trial, the subject-selection procedure, and
the rights, safety, and well being of the subjects
participating in the trial
,2|Page
Which of the following documents is the investigator
obliged to comply with during the trial? - Answer-All
applicable laws and regulations, ICH-GCP, and the trial
protocol
What is the purpose of the initiation visit? - Answer-To
review the protocol, to review the blank case report forms
(CRFs), and to review standard procedures
Who is ultimately responsible for Source Data Verification
(SDV)? - Answer-The monitor
Every research study involving human subjects must be
registered in a publicly accessible database before
recruitment of the first subject (T/F). - Answer-True
The Declaration of Helsinki was developed by: - Answer-
the WMA
This phase determines therapeutic benefit and is usually
done in larger, specific population: - Answer-Phase 3
, 3|Page
Therapeutic use & begins after drug approval. - Answer-
Phase 4
A sponsor can be defined as... - Answer-Phase 1
Providing a unified standard for Europe, US, and Japan to
facilitate the acceptance of clinical trials is the.. - Answer-
Mission statement of the ICH
A sub-investigator can be defined as.. - Answer-Any
individual member of the clinical trial team designated and
supervised by the investigator of a trial site to perform
clinical trial related procedures and/or to make important
trial related decisions
According to the principles of ICH GCP... - Answer-1.
Clinical trials should be conducted in accordance with the
ethical principles that have their origin in the DoH and that
are consistent with GCP and the applicable regulatory
requirement(s)
2. Before a trial is initiated, foreseeable risks and
inconveniences should be weighted against the
anticipated benefit for the individual trial subject and
ACRP CP CERTIFICATION EXAM LATEST 2026
ACTUAL EXAM WITH COMPLETE QUESTIONS AND
CORRECT DETAILED ANSWERS ||VERIFIED
EXAM!!!(100% VERIFIED ANSWERS) |ALREADY
GRADED A+| ||PROFESSOR VERIFIED|| ||NEWEST
EXAM!!!!!!||
In any trial, what should be the main concern of the
physician? - Answer-The welfare of the subjects
The world medical association (WMA) ethical principles for
medical research involving human subjects is called: -
Answer-The Declaration of Helsinki
The process by which a subject voluntarily confirms his or
her willingness to participate in a clinical trial is known as:
- Answer-Informed Consent of Trial Subjects
What does the IRB/IEC evaluate? - Answer-The scientific
tenability of the trial, the subject-selection procedure, and
the rights, safety, and well being of the subjects
participating in the trial
,2|Page
Which of the following documents is the investigator
obliged to comply with during the trial? - Answer-All
applicable laws and regulations, ICH-GCP, and the trial
protocol
What is the purpose of the initiation visit? - Answer-To
review the protocol, to review the blank case report forms
(CRFs), and to review standard procedures
Who is ultimately responsible for Source Data Verification
(SDV)? - Answer-The monitor
Every research study involving human subjects must be
registered in a publicly accessible database before
recruitment of the first subject (T/F). - Answer-True
The Declaration of Helsinki was developed by: - Answer-
the WMA
This phase determines therapeutic benefit and is usually
done in larger, specific population: - Answer-Phase 3
, 3|Page
Therapeutic use & begins after drug approval. - Answer-
Phase 4
A sponsor can be defined as... - Answer-Phase 1
Providing a unified standard for Europe, US, and Japan to
facilitate the acceptance of clinical trials is the.. - Answer-
Mission statement of the ICH
A sub-investigator can be defined as.. - Answer-Any
individual member of the clinical trial team designated and
supervised by the investigator of a trial site to perform
clinical trial related procedures and/or to make important
trial related decisions
According to the principles of ICH GCP... - Answer-1.
Clinical trials should be conducted in accordance with the
ethical principles that have their origin in the DoH and that
are consistent with GCP and the applicable regulatory
requirement(s)
2. Before a trial is initiated, foreseeable risks and
inconveniences should be weighted against the
anticipated benefit for the individual trial subject and
