DEVICE RAC EXAM (New 2026/ 2027
Update) Questions & Answers 100%
Correct (Verified Solutions) - {Grade A}
The Quality System Regulation (QSR) for medical devices (21CFR 820) pertains to the
manufacturing of which of the following:
A) Finished devices, but not accessories
B) Finished devices and components of finished devices
C) Finished devices and accessories to finished devices
D) Finished devices, components, and accessories to finished devices - Correct
answer C
The QSR for Class III devices applies to the following except:
A) Critical component manufacturers
B) Operations done by the manufacturer at facilities located in the United States
C) Research on investigational devices tested outside of the United States
D) Contract Sterilizers - Correct answer A
,The QSR for medical devices (21CFR 820) requires all of the following except:
A) Management to make a commitment to quality
B) A Quality Plan that defines how quality will be met
C) Management must review the Quality System at least quarterly
D) A Quality representative must be identified and documented - Correct answer C
The QSR for medical devices regarding Design Controls require which of the following:
A) Documentation of early research of the design
B) Design and development plans address how design inputs and requirements are
managed
C) A product design can be outsourced by a manufacturer so they do not have to
maintain the documentation
D) Design activities are only required for Class III Investigational devices - Correct
answer B
,Design Control "verification" requires which of the following:
A) The product design meets the users needs
B) The process produces a product that meets predetermined specifications
C) The product design meets specified requirements
D) The product design meets the intended use requirements - Correct answer C
According to the QSR, Design Inputs are best described by the following:
A) The Operator's Manual and instructions on how to use the device
B) The Instructions For Use (IFU) of the device
C) Marketing claims and features that are required for the device
D) The performance requirements that the product must meet - Correct answer D
According to the QSR, Design Outputs contain the following:
A) The Device Master Record (DMR)
B) The documentation from the last phase of the complete Design Control process
, C) The test reports that support that the Design Inputs have been met
D) All of the packaging and labeling associated with the finished device
E) A and D above - Correct answer E
According to the QSR, Quality Audits must accomplish the following:
A) Meet the same requirements of the original GMP
B) Evaluate if the Quality System is in compliance with the QSR
C) Determine the effectiveness of the Quality System
D) Focus on Design Controls and the CAPA system
E) B and C above
F) A and D above - Correct answer E
According to the QSR, personnel involved in the design, manufacture, distribution,
servicing, and reporting must:
A) Must hold a Master's degree or higher
Update) Questions & Answers 100%
Correct (Verified Solutions) - {Grade A}
The Quality System Regulation (QSR) for medical devices (21CFR 820) pertains to the
manufacturing of which of the following:
A) Finished devices, but not accessories
B) Finished devices and components of finished devices
C) Finished devices and accessories to finished devices
D) Finished devices, components, and accessories to finished devices - Correct
answer C
The QSR for Class III devices applies to the following except:
A) Critical component manufacturers
B) Operations done by the manufacturer at facilities located in the United States
C) Research on investigational devices tested outside of the United States
D) Contract Sterilizers - Correct answer A
,The QSR for medical devices (21CFR 820) requires all of the following except:
A) Management to make a commitment to quality
B) A Quality Plan that defines how quality will be met
C) Management must review the Quality System at least quarterly
D) A Quality representative must be identified and documented - Correct answer C
The QSR for medical devices regarding Design Controls require which of the following:
A) Documentation of early research of the design
B) Design and development plans address how design inputs and requirements are
managed
C) A product design can be outsourced by a manufacturer so they do not have to
maintain the documentation
D) Design activities are only required for Class III Investigational devices - Correct
answer B
,Design Control "verification" requires which of the following:
A) The product design meets the users needs
B) The process produces a product that meets predetermined specifications
C) The product design meets specified requirements
D) The product design meets the intended use requirements - Correct answer C
According to the QSR, Design Inputs are best described by the following:
A) The Operator's Manual and instructions on how to use the device
B) The Instructions For Use (IFU) of the device
C) Marketing claims and features that are required for the device
D) The performance requirements that the product must meet - Correct answer D
According to the QSR, Design Outputs contain the following:
A) The Device Master Record (DMR)
B) The documentation from the last phase of the complete Design Control process
, C) The test reports that support that the Design Inputs have been met
D) All of the packaging and labeling associated with the finished device
E) A and D above - Correct answer E
According to the QSR, Quality Audits must accomplish the following:
A) Meet the same requirements of the original GMP
B) Evaluate if the Quality System is in compliance with the QSR
C) Determine the effectiveness of the Quality System
D) Focus on Design Controls and the CAPA system
E) B and C above
F) A and D above - Correct answer E
According to the QSR, personnel involved in the design, manufacture, distribution,
servicing, and reporting must:
A) Must hold a Master's degree or higher
