eCFR Reference Browser

---

title: "21 CFR §111.13"

source: "https://www.ecfr.gov/current/title-21/section-111.13"

title_number: "21"

volume_number: "2"

chapter_number: "Unknown"

subchapter_code: "B"

subchapter_subject: "FOOD FOR HUMAN CONSUMPTION"

part_code: "111"

part_subject: "CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS"

subpart_code: "B"

subpart_subject: "Personnel"

section_number: "111.13"

section_subject: "What supervisor requirements apply?"

cfr_reference: "21 CFR 111.13"

title_name: "Title 21"

title_subject: "Food and Drugs"

parts_covered: "Parts 100 to 169"

revised_date: "Revised as of April 1, 2019"

publication_date: "As of April 1, 2019"

contains_description: "Containing a codification of documents of general applicability and future effect"

publication_info: "Published by the Office of the Federal Register National Archives and Records Administration as a Special Edition of the Federal Register"

---

(a)You must assign qualified personnel to supervise the manufacturing, packaging, labeling, or holding of dietary supplements.

(b)Each supervisor whom you use must be qualified by education, training, or experience to supervise.

§111.13 - What supervisor requirements apply?