10.5 - Laboratory Physical and Chemical Testing 211.65 SOP and report form for

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

or holding of a drug product shall be maintained in a clean and sanitary condition

Quantitative test methods must be validated by determining in assays the sensitivity

Any surfaces that contact components

or label to make it suitable for use in the manufacture of a dietary supplement unless Quality control personnel conduct a material review and make a disposition decision to approve this

10.5 - Laboratory Physical and Chemical Testing 211.65 SOP and report form forWet 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