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GMP-documentatie
IQ & OQ – Installation & Operation Qualification
The following IQ / OQ is intended
to be a guideline, local IQ / OQ
procedures can vary depending on
application and items stored in the
Gram BioLine cabinet.
Deviations from the specifications
dictated in the PQ are to be
reported in the deviation report.
The PQ is concluded if all criteria of
acceptance are approved and the
possible deviations are rectified or
accepted.
64
Organisation:
Location of installation:
Model:
Serial number:
Item and revision number of instructions for use:
Status of operation:
Active
Inactive
Name of vendor:
Warranty:
Start:
________________________________________________
End:
________________________________________________
Model: ________________________
SN: ________________________
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