CCRP SOCRA Exam | 100% Correct
Answers | Verified | Latest 2024 Version
The responsibility for ensuring that the investigator understands a clinical trial lies with which
individual/or organization?
A) FDA
B) IRB
C) Sponsor
D) Coordinator
C) Sponsor
What is the minimum number of IRB Members?
A) 3
B) 5
C) 6
D) 10
B) 5
A significant risk device is defined as an investigational device that is:
A) Intended as an implant and presents a potential for serious risk to the health, safety, or welfare of a
subject
B) Purported or represented to be for a use in supporting or sustaining human life and presents a
potential risk to the health, safety, or welfare of a subject
,C) For a use of substantial importance in diagnosing, curing, mitigating, or treating disease, or otherwise
preventing impairment of human health and presents a potential for serious risk to the health, safety, or
welfare of a subject.
D) All the above
D ) All of the above
With respect to IRB/IEC membership, both the FDA and the ICH require that:
A) A majority of the members' primary area of interest is in a scientific area
B) At least one member holds a Ph.D. degree or equivalent
C) At least one member's primary area of interest is in a nonscientific area
D) A majority of the members are from or have ties to the institution of record
C) At least one member's primary area of interest is in a nonscientific area
In a non-emergency situation, under which of the following conditions, if any, may subjects been rolled
into a study prior to IRB/IEC approval?
A) The investigator provides his/her written approval
B) The study drug has an FDA approved marketing application
C) The FDA provides written approval of the IND
D) Subjects cannot be enrolled until IRB/IEC approval has been obtained
D) Subjects cannot be enrolled until IRB/IEC approval has been obtained
, A subject has been enrolled on a study and was randomized to the non-treatment arm. The protocol
outlines study procedures for all subjects to be performed within one week of enrollment. Which of the
following statements about this case is correct?
A) This subject does not need to undergo any of the study procedures since the subject is enrolled on
the non-treatment arm
B) This subject should undergo all study procedures as outlined in the protocol
C) This subject only needs to undergo the study procedures that pertain specifically to the subject
D) This subject can undergo the study procedures whenever it is convenient
B) This subject should undergo all study procedures as outlined in the protocol
A purpose of monitoring clinical trials is to verify that:
A) The rights, safety, and well-being of human subjects are protected
B) Investigators receive adequate payment for their participation in the clinical trial
C) The investigator has received annual reports from the sponsor
D) The regulatory agency has received all case history information of subjects enrolled on the clinical trial
A) The rights, safety, and well-being of human subjects are protected
Which of the following is the proper way to make a correction to a CRF?
A) Completely blacken the incorrect entry and then enter the correct information
Answers | Verified | Latest 2024 Version
The responsibility for ensuring that the investigator understands a clinical trial lies with which
individual/or organization?
A) FDA
B) IRB
C) Sponsor
D) Coordinator
C) Sponsor
What is the minimum number of IRB Members?
A) 3
B) 5
C) 6
D) 10
B) 5
A significant risk device is defined as an investigational device that is:
A) Intended as an implant and presents a potential for serious risk to the health, safety, or welfare of a
subject
B) Purported or represented to be for a use in supporting or sustaining human life and presents a
potential risk to the health, safety, or welfare of a subject
,C) For a use of substantial importance in diagnosing, curing, mitigating, or treating disease, or otherwise
preventing impairment of human health and presents a potential for serious risk to the health, safety, or
welfare of a subject.
D) All the above
D ) All of the above
With respect to IRB/IEC membership, both the FDA and the ICH require that:
A) A majority of the members' primary area of interest is in a scientific area
B) At least one member holds a Ph.D. degree or equivalent
C) At least one member's primary area of interest is in a nonscientific area
D) A majority of the members are from or have ties to the institution of record
C) At least one member's primary area of interest is in a nonscientific area
In a non-emergency situation, under which of the following conditions, if any, may subjects been rolled
into a study prior to IRB/IEC approval?
A) The investigator provides his/her written approval
B) The study drug has an FDA approved marketing application
C) The FDA provides written approval of the IND
D) Subjects cannot be enrolled until IRB/IEC approval has been obtained
D) Subjects cannot be enrolled until IRB/IEC approval has been obtained
, A subject has been enrolled on a study and was randomized to the non-treatment arm. The protocol
outlines study procedures for all subjects to be performed within one week of enrollment. Which of the
following statements about this case is correct?
A) This subject does not need to undergo any of the study procedures since the subject is enrolled on
the non-treatment arm
B) This subject should undergo all study procedures as outlined in the protocol
C) This subject only needs to undergo the study procedures that pertain specifically to the subject
D) This subject can undergo the study procedures whenever it is convenient
B) This subject should undergo all study procedures as outlined in the protocol
A purpose of monitoring clinical trials is to verify that:
A) The rights, safety, and well-being of human subjects are protected
B) Investigators receive adequate payment for their participation in the clinical trial
C) The investigator has received annual reports from the sponsor
D) The regulatory agency has received all case history information of subjects enrolled on the clinical trial
A) The rights, safety, and well-being of human subjects are protected
Which of the following is the proper way to make a correction to a CRF?
A) Completely blacken the incorrect entry and then enter the correct information
