21 CFR 111.13
§ 111.13 What supervisor requirements apply?
United States · 21 CFR — Food and Drugs · Status: effective
Cite this
- Citation
- 21 CFR 111.13, § 111.13 What supervisor requirements apply?, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/84131
- Permanent ID
ys:prov:84131@1- SHA-256
90e8b60a0565ee75c778857ebb191da54fe5f0a1fd0fd79e426e237652677653
The hash is SHA-256 of this version's text, with every run of whitespace collapsed to a single space and the ends trimmed. The ID always leads back here, and checking it says whether the text you cited is still the current version.
Full text
(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.
Legislative history
This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.