21 CFR § 226.10

21 CFR · Food and Drugs

§ 226.10 — Personnel.

21 CFR § 226.10

TitleTitle 21: Food and Drugs PartPart 226: Current Good Manufacturing Practice for Type a Medicated Articles

SourceeCFR (current through Apr 9, 2026)

This text of 21 C.F.R. § 226.10 (Personnel.) is published on Counsel Stack Legal Research, covering United States primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook

21 C.F.R. § 226.10 (2026).

Text

§ 226.10 Personnel.
The key personnel and any consultants involved in the manufacture and control of the Type A medicated article(s) shall have a background of appropriate education or appropriate experience or combination thereof for assuming responsibility to assure that the Type A medicated article(s) has the proper labeling and the safety, identity, strength, quality, and purity that it purports to possess.

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§ 226.10 Personnel.

The key personnel and any consultants involved in the manufacture and control of the Type A medicated article(s) shall have a background of appropriate education or appropriate experience or combination thereof for assuming responsibility to assure that the Type A medicated article(s) has the proper labeling and the safety, identity, strength, quality, and purity that it purports to possess.