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components
Such specifications must be met
SOP and report form for tablet or capsule dissolution testing of by Quality Control according to USP <711> and EP 2
must be verified for each sample matrix by qualified personnel
or hold components of dietary supplements using approved chemical agents at the required frequency to prevent contamination
16.0 - GMP Records for Supplements supplier approval componentsYou must keep written records required by this part for 1 year past the shelf life date, if shelf life dating is used, or 2 years beyond the date of distribution of the last batch of dietary supplements associated with those records. You must have all records required readily available during the retention period for inspection and copying by FDA when requested
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