21 CFR § 111.103 Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements

§ 111.103 What are the requirements under this subpart F for written procedures?

Current through Sep 8, 2026 · Read all of Part 111

You must establish and follow written procedures for the responsibilities of the quality control operations, including written procedures for conducting a material review and making a disposition decision, and for approving or rejecting any reprocessing.

← § 111.95 Under this subpart E, what records must you make and keep?§ 111.105 What must quality control personnel do? →