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or holding of a drug product shall be maintained in a clean and sanitary condition
performed during the development of a new drug product
must be verified for each sample matrix by qualified personnel
Equipment must be adequately maintained as part of a preventive maintenance program to protect components and dietary supplements from being contaminated by any source
EP or other recognised test methods
USP 621 Thin Layer Chromatography glp records or holding of a drugSOP for the use of TLC by Quality Control to separate mixtures of compounds or analytes using a solvent mobile phase and plate to confirm presence or purity of a substance
US$ 55.00
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