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or holding of a drug product shall be maintained in a clean and sanitary condition
if errors have occurred
and the authority to review production records to assure that no errors have occurred or
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for example AOAC
USP 1216 Friability of Tablets tlc or holding of a drugSOP and report form for the friability testing by Quality Control to determine if a tablet with chip, crumble, or break under compression during storage or transport