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There shall be separate or defined areas necessary to prevent contamination or mix-ups during receipt
or examination by the quality control unit before release for manufacturing
drug product containers
packaging material
if shelf life dating is used
USP 62 Absence of Staph Aureus 2.2.8 There shall be separate orProcedure and report form for testing the absence or presence of staphylococcus aureus in products or materials by Quality Control according to USP <62> and EP 2. 6. 13 and to the limits specified in USP <1111> and EP 5. 1. 4
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