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Quality Control must review all complaints to determine the potential failure of a drug product to meet any of its specifications and whether the complaint represents a serious and unexpected adverse drug experience which is required to be reported to competent authorities in the country where it is marketed
and composition of the finished batch
properly storing and disposing of equipment and trash
You must have all records required readily available during the retention period for inspection and copying by FDA when requested
of materials or drug product must be examined visually for appropriate labeling as to contents
4.2 - Equipment Cleaning and Sanitizing gdp Quality Control must review allYou must maintain, clean, and sanitize, as necessary, all equipment, utensils, and any other contact surfaces used to manufacture, package, label, or hold components of dietary supplements using approved chemical agents at the required frequency to prevent contamination
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