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Deviation Management



Dear All,

Can anybody please guide what are the advantagges of Reporting / documenting the "Deviations" arised due to non functioning / malfunctioning of process instruments.

e.g. If a particular probe is not sensing the required process control parameter, Do we have to fill a deviation as we are tracking internally its replacement, then need we generate a deviation form for it?


Thanks in advance,
Ambika.

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