Q5 W6 Flashcards

1
Q

Yield calculated electronically do not require second person verification.

False
True

A

False

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2
Q

Deviation description, justification, investigation of root causes, CAPAs, and evaluations are all a part of:

Investigation Report
AQL
Batch Record
Nonconformance
Statistical Sampling

A

Investigation Report

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3
Q

______________________was made to specify the acceptable positions of the spray nozzles on the spray arm.

Equipment Master File
Master Batch Record
Deviation Report Form
SOP
Executed Batch Record

A

Equipment Master File

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4
Q

Theoretical and expected yields are to be included in:

Master Batch Record
Executed Batch Record
SOP
Batch Record
Conclusion of Process

A

Master Batch Record

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5
Q

AQL stands for:

Acceptable Quality Limit
Acceptable Quantity Limit
Acceptable Quality List
Acceptable Quantity Level
Assurance Quality Limit

A

Acceptable Quality Limit

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6
Q

The weight of a in-process material removed from a reactor was 1.2 kg greater than the weight of materials charged because…

Condense toluene increased vent pressure
Calculations were off
Verifier wasn’t paying attention
Scale calibration was off
Disharged material Toluene was not accounted for in the process

A

Condense toluene increased vent pressure

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7
Q

If a result falls outside of established acceptance criteria or set specifications then this is called:

Out of specification
Deviation
Investigation
Nonconformance
Defect

A

Out of specification

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8
Q

Which of these is considered a Major defect?

Low tablet count
Wrong lot number
Crooked label
Wrong tablets
Too many tablets per blister

A

Low tablet count

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9
Q

The total number of defects must be ___________ the limit as defined by AQL ANSI.

A

less than

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10
Q

Please read carefully…Only choose one to answer…DO NOT ANSWER BOTH or YOU WILL NOT GET FULL POINTS.

A. What does CAPA stand for AND what is the purpose of them? OR

B. In your own words, describe how the thermocouple got coated.

A

CAPA stands for “Corrective Action Preventative Action” or “Corrective And Preventative Action.” They are used when there are deviations and are put into Investigation Reports. The purpose of CAPA is to first correct issues with a current batch and then figure out how to prevent issues in future batches.

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