ACRP PRACTICE EXAM BUNDLE 2026
QUESTIONS WITH COMPLETE SOLUTIONS
⩥ Audit. Answer: Reviews how the research was conducted; takes into
account SOPs, IRB requirements & GCP (ensures compliance)
⩥ Audit Certificate. Answer: Confirmation audit took place
⩥ Audit Report. Answer: Written Evaluation - not regularly made
available to regulatory body; only when serious evidence exists
concerning non-compliance
⩥ Audit Trail. Answer: Documentation of audit events
⩥ Single Blind Study. Answer: Subjects Unaware
⩥ Double Blind Study. Answer: Subjects & Researchers are unaware
⩥ Comparator. Answer: Item used as an active control references in a
clinical trail
⩥ Coordinating Committee. Answer: Group a sponsor comprises to
coordinate multi-center trials
,⩥ Coordinating Investigator. Answer: An investigator who oversees
multiple sites of a clinical trial (multicenter)
⩥ IDMC. Answer: Independent Data Monitoring Committee, Data &
Safety Monitoring Board (DSMB), Data Monitoring Committee:
Oversee safety & progress; make recommendations to continue, modify
or stop
⩥ IEC. Answer: Independent Ethics Committee; group who oversees
protection, rights, safety & well-being of human subjects
⩥ Investigator's Brochure. Answer: Compilation of data on an
investigational product used in human subjects
⩥ Legally acceptable representative. Answer: person whom is lawfully
able to consent on behalf of another
⩥ SAE. Answer: Serious Adverse Event - Results in death, is life-
threatening, requires long-term hospitalization, results in long term
disability/hospitalization incapacitation or is a congenital birth defect
⩥ Source data. Answer: original clinical information from source
documents (medical record information)
,⩥ Vulnerable subjects. Answer: *Hierarchical structure employees
*armed forces
*detainees
*incurable disease pts
*homeless
*poor
*those in nursing home
*minors
*those unable to give consent
⩥ ICH. Answer: International Conference on Harmonization
⩥ Principles of ICH & GCP. Answer: *Protect research subjects
*conduct research as it has been approved
*research should be clear, organized & approved by an IRB/IEC
⩥ IRB / IEC Responsibilities. Answer: *Oversee principles of ICH/GCP
*Make sure the PI / Co-Is are qualified
* Review studies at least once a year
⩥ Requirements of an IRB. Answer: * at least 5 members
* one non-scientific member
, * one non-institute member
⩥ What needs reported to the IRB?. Answer: *Changes / deviations from
protocol due to unforeseen hazard
* changes to subject risk
* adverse events
* new info that may impact subject safety
⩥ Payment to subjects must be..... Answer: prorated & not contingent on
subject completing study
⩥ Investigator Responsibilities. Answer: *Maintain delegation long
*Ensure staff are trained/informed about the protocol (give delegated
tasks)
* Ascertain reason study participant withdraws consent while respecting
their privacy & rights
* Adhere to approved protocol
*Document & explain any deviations from approved protocol
* Process protocol amendments according to GCP
*Manage proper storage & care for trial devices/drugs. (PI can delegate
this task to trained professional - PharmD, etc)
⩥ Protocol amendments should be submitted to. Answer: 1. IRB
QUESTIONS WITH COMPLETE SOLUTIONS
⩥ Audit. Answer: Reviews how the research was conducted; takes into
account SOPs, IRB requirements & GCP (ensures compliance)
⩥ Audit Certificate. Answer: Confirmation audit took place
⩥ Audit Report. Answer: Written Evaluation - not regularly made
available to regulatory body; only when serious evidence exists
concerning non-compliance
⩥ Audit Trail. Answer: Documentation of audit events
⩥ Single Blind Study. Answer: Subjects Unaware
⩥ Double Blind Study. Answer: Subjects & Researchers are unaware
⩥ Comparator. Answer: Item used as an active control references in a
clinical trail
⩥ Coordinating Committee. Answer: Group a sponsor comprises to
coordinate multi-center trials
,⩥ Coordinating Investigator. Answer: An investigator who oversees
multiple sites of a clinical trial (multicenter)
⩥ IDMC. Answer: Independent Data Monitoring Committee, Data &
Safety Monitoring Board (DSMB), Data Monitoring Committee:
Oversee safety & progress; make recommendations to continue, modify
or stop
⩥ IEC. Answer: Independent Ethics Committee; group who oversees
protection, rights, safety & well-being of human subjects
⩥ Investigator's Brochure. Answer: Compilation of data on an
investigational product used in human subjects
⩥ Legally acceptable representative. Answer: person whom is lawfully
able to consent on behalf of another
⩥ SAE. Answer: Serious Adverse Event - Results in death, is life-
threatening, requires long-term hospitalization, results in long term
disability/hospitalization incapacitation or is a congenital birth defect
⩥ Source data. Answer: original clinical information from source
documents (medical record information)
,⩥ Vulnerable subjects. Answer: *Hierarchical structure employees
*armed forces
*detainees
*incurable disease pts
*homeless
*poor
*those in nursing home
*minors
*those unable to give consent
⩥ ICH. Answer: International Conference on Harmonization
⩥ Principles of ICH & GCP. Answer: *Protect research subjects
*conduct research as it has been approved
*research should be clear, organized & approved by an IRB/IEC
⩥ IRB / IEC Responsibilities. Answer: *Oversee principles of ICH/GCP
*Make sure the PI / Co-Is are qualified
* Review studies at least once a year
⩥ Requirements of an IRB. Answer: * at least 5 members
* one non-scientific member
, * one non-institute member
⩥ What needs reported to the IRB?. Answer: *Changes / deviations from
protocol due to unforeseen hazard
* changes to subject risk
* adverse events
* new info that may impact subject safety
⩥ Payment to subjects must be..... Answer: prorated & not contingent on
subject completing study
⩥ Investigator Responsibilities. Answer: *Maintain delegation long
*Ensure staff are trained/informed about the protocol (give delegated
tasks)
* Ascertain reason study participant withdraws consent while respecting
their privacy & rights
* Adhere to approved protocol
*Document & explain any deviations from approved protocol
* Process protocol amendments according to GCP
*Manage proper storage & care for trial devices/drugs. (PI can delegate
this task to trained professional - PharmD, etc)
⩥ Protocol amendments should be submitted to. Answer: 1. IRB
