Title Page
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Site conducted
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Conducted on
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Facility and Department
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Prepared by
Procedures
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Have all staff received orientation and/or an annual update on vaccine management?
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Has the vaccine management policy been reviewed as required and is up to date?
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Is graph/logbook/chart for temperature recording readily available?
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Is the temperature of the vaccine refridgerator recorded twice a day when the facility is open?
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Are the contact numbers to report a cold chain breach easily accessible
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Were all deviations outside the +2°C to +8°C range reported to pharmacy and IC manager
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Have the responses to all deviations outside the +2°C to +8°C range been documented and recommended actions taken?
Equipment
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Has the refrigerator shown evidence of malfunction (eg poor seals so that the door opens too easily)?
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Has corrective action been taken?
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Is there an appropriate gap between the vaccines and the walls of the refrigerator?
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Can the refrigerator continue to store the required volume of vaccines safely according to these guidelines? (This includes times of increased demand such as the influenza program.)
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Does the power outlet have a sign ‘Do not turn off or disconnect this refrigerator’?
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Is the refrigerator plugged into a red OR blue power point?
Monitoring equipment
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Has the refrigerator been serviced in the past 6 months?
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Date and results of last Thermometer accuracy check:
Alternative vaccine storage
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Is there a readily accessible written procedure for what to do during a power failure?
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Is enough alternative storage (eg cooler, other monitored refrigerator) available for vaccine storage, if necessary (eg vaccine refrigerator breakdown or power failure)?
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Are ice packs/gel packs at the correct temperature available?
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Is there one minimum/maximum thermometer for each cooler?
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Is there enough insulating material for each cooler?
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