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Code · CFR · Title 21 — Food and Drugs · Part 111 — Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements · § 111.60

§ 111.60. What are the design requirements for the production and process control system?

80 words·~1 min read·/us/cfr/t21/s§ 111.60·

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(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
(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.
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