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Each holder of a manufacturing authorization should have a quality control department. The independence of quality control from production and other departments is considered fundamental to the satisfactory operation of quality control. This department is under the authority of a person with appropriate qualifications and experience.
The Quality Control duties pertain (not exclusive) to establishing, validating and implementing all quality control procedures, evaluating, maintaining and storing the reference standards of substances, ensuring the correct labeling of containers of materials and products, ensuring the monitoring of the stability of the active pharmaceutical substances and the products, participating in the investigation of complaints related to the quality of the product,-----etc. |
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