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21CFR226.10

§ 226.10 Personnel.

Regulation Text

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.

Authority

21 U.S.C. 351,352,360b,371,374.

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21CFR226.10 — § 226.10 Personnel. | CFR Explorer | BioRegHub