StacksVerified U.S. regulatory reference

21 CFR §111.60

Verified against eCFR.gov as of June 20, 2026View official text on eCFR.gov ↗
  1. (a)Your production and in-process control system must be designed to ensure that the dietary supplement is manufactured, packaged, labeled, and held in a manner that will ensure the quality of the dietary supplement and that the dietary supplement is packaged and labeled as specified in the master manufacturing record; and
  2. (b)The production and in-process control system must include all requirements of subparts E through L of this part and must be reviewed and approved by quality control personnel.