10.5 - Laboratory Physical and Chemical Testing 211.65 or holding of a drug

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

the appropriateness of current specifications for both starting materials and finished product

You must use adequate laboratory facilities to perform whatever testing and examinations are necessary to determine that specifications are met

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 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