Logistics Manager (August Update)
/by Alex Ashton
Now please take the following quiz to show your understanding of the updated processes.
Good Luck!
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Question 1 of 10
1. Question
What temperatures are regarding as being extreme with regard to leaving blood samples in the IDEXX mailbox or PBB drop box?
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Question 2 of 10
2. Question
Bubble wrap should be left in the cool boxes after the blood units have been removed in order to save time ahead of the next session. True or False?
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Question 3 of 10
3. Question
When might a minor non-conformance trigger the CAPA process?
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Question 4 of 10
4. Question
A non-conformance record (FRM/QUA/04) doesn’t need to be completed if the non-conformance risk category is under 2. True or False?
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Question 5 of 10
5. Question
Once a non-conformance record has been completed or has been moved to CAPA who must review the non-conformance?
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Question 6 of 10
6. Question
Who’s the appropriate person to speak to regarding the recall of a non-blood product?
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Question 7 of 10
7. Question
If there is a electronic notification of a product quality issue who needs to be notified?
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Question 8 of 10
8. Question
Any member of staff should complete a Potential Non Conformance Report containing all of the required information , if they identify a non conformance. True or False?
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Question 9 of 10
9. Question
Once a CAPA action plan has been approved, it is the responsibility of the Quality Department to communicate the plan out to all relevant personnel via email. True or False?
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Question 10 of 10
10. Question
When placing goods into quarantine, goods should be labelled with a quarantine label or sticker. True or False?
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