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by Quality Control according to USP <1217> and EP 2
or deterioration
formality and documentation of the quality risk management process is commensurate with the level of risk
performed maximum annually once the drug is marketed
USP 62 Absence of Salmonella bile tolerant by Quality Control according toSOP and report form for testing for the absence or presence of Salmonella in products or materials according to USP <62> and EP 2. 6. 13 and to limits specified in USP <1111> and EP 5. 1. 4
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