VAL MANUAL- 061 Cleaning Validation and Verification of Equipments Used for Manufacturing Active Pharmaceutical Ingredients
Microbiological aspects of cleaning are not considered in detail in this guideline. The risk of microbiological contamination and the associated actions to mitigate this risk should be assessed on a case-by-case basis, eg generally equipment is not left wa
VAL MANUAL- 061 Cleaning Validation and Verification of Equipment Used for Manufacturing Active Pharmaceutical Ingredients
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