Journal of Validation Technology Once products have been grouped and worst case(s) selected, the next logical question to be answered is "How much product can remain on equipment?". There are many bases for establishing limits for cleaning processes. Some of them are.
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Validation of the Autoclave is classified into the following 1.0 OQ – Operational Qualification 2.0 PQ – Performance Qualification The valid... -
K. Dashora, D. Singh, Swarnlata Saraf and S. Saraf *. Institute of Pharmacy, Pt.RavishankarShuklaUniversity, Raipur 492 010. *Author for ...
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2.0 Scope: Final visual inspection is performed manually by human operators. Prior to being qualified as an inspector, each in...
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