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5.2 - Materials - Receipt and Storage lab specifications contamination

SKU: 80233200077

4.6
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Description

contamination

covered by a marketing authorisation

Equipment used in the production or holding of a drug product shall be of appropriate design

quality or efficacy

You must identify and use an appropriate scientifically valid method for each established specification for which testing or examination is required to determine whether the specification is met

5.2 - Materials - Receipt and Storage lab specifications contaminationUpon receipt, each container, or group of containers, of materials or drug product must be examined visually for appropriate labeling as to contents, container damage or broken seals, and contamination. Thereafter they must be stored under quarantine until they have been tested or examined, and released, then stored without mix up or contamination

Exchange/Return Notes
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