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Outrage Temperature Incidents An outrage temperature incident, also called a temperature excursion, refers to any storage temperature outside the recommended range for a vaccine. The TOTAL amount
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How to fill out handling a temperature excursion
How to fill out handling a temperature excursion
01
Identify the temperature excursion by monitoring temperature logs and alarms.
02
Determine the cause of the temperature excursion.
03
Take corrective actions to bring the temperature back to the required range.
04
Document the temperature excursion, including the cause, actions taken, and any impact on products.
05
Notify relevant stakeholders about the temperature excursion and the actions taken.
Who needs handling a temperature excursion?
01
Any organization or individual handling temperature-sensitive products such as pharmaceuticals, food items, chemicals, and biological samples needs to handle a temperature excursion to ensure product safety and efficacy.
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What is handling a temperature excursion?
Handling a temperature excursion involves taking action to address an unexpected increase or decrease in temperature during the storage or transportation of temperature-sensitive products.
Who is required to file handling a temperature excursion?
The individuals responsible for the storage or transportation of temperature-sensitive products are required to file a report on handling a temperature excursion.
How to fill out handling a temperature excursion?
To fill out a report on handling a temperature excursion, one must document the details of the temperature deviation, the actions taken to address it, and any impact on the quality of the products.
What is the purpose of handling a temperature excursion?
The purpose of handling a temperature excursion is to ensure the safety and efficacy of temperature-sensitive products by addressing any deviations from the recommended storage or transportation conditions.
What information must be reported on handling a temperature excursion?
The report on handling a temperature excursion must include details of the deviation, the products involved, the corrective actions taken, and any impact on product quality.
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