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or holding of a drug product shall be maintained in a clean and sanitary condition
SOP and report form for the melting point determination of solid and semi-solid samples by Quality Control according to USP <741> and EP 2
at intervals following a pre-arranged programme in order to verify their conformity with the principles of Quality Assurance
dietary supplements and labels in a manner that does not lead to their mix-up
10.5 - Laboratory Physical and Chemical Testing 211.65 or holding of a drugWet chemistry requirements of the Quality Control (QC) Laboratory with respect to written procedures and specifications, equipment, calibration, sampling, reagents, standards, and glassware, in order to perform USP, EP or other recognised test methods, or validated in house methods
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