5.2 - Materials - Receipt and Storage lab specifications covered by a marketing authorisation

covered by a marketing authorisation

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

The level of supervision must be proportional to the risk posed by the individual materials

quality or efficacy

5.2 - Materials - Receipt and Storage lab specifications covered by a marketing authorisationUpon 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