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Methods requiring validation must be added to the VMP
and at the frequency specified in writing by the manufacturer of the instrument and control
You must verify that the laboratory examination and test methods are appropriate for their intended use for each supplement or drug
Labeling materials issued for a batch shall be carefully examined for identity and conformity to the labeling specified in the master or batch production records
containers
6.0 - Production Overview batch record Methods requiring validation must beThere shall be written procedures for production and process control designed to assure that the drug products have the correct identity, strength, quality, and purity. These must be followed and documented at the time of performance. Any deviation from the written procedures shall be recorded and justified