21 CFR § 226.10 - Personnel.

---
identifier: "/us/cfr/t21/s226.10"
source: "ecfr"
legal_status: "authoritative_unofficial"
title: "21 CFR § 226.10 - Personnel."
title_number: 21
title_name: "Food and Drugs"
section_number: "226.10"
section_name: "Personnel."
chapter_name: "FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES"
subchapter_number: "C"
subchapter_name: "DRUGS: GENERAL"
part_number: "226"
part_name: "CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES"
positive_law: false
currency: "2026-04-05"
last_updated: "2026-04-05"
format_version: "1.1.0"
generator: "[email protected]"
authority: "21 U.S.C. 351, 352, 360b, 371, 374."
regulatory_source: "40 FR 14031, Mar. 27, 1975, unless otherwise noted."
cfr_part: "226"
---


# 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.