21 CFR Part 211 - Current Good Manufacturing Practice
Subpart B - Organization and Personnel

21 CFR Part 211 - Current Good Manufacturing Practice CFR211-B-22: Section 211.22 - Responsibilities of Quality Control Unit

A quality control unit with authority and responsibility to approve or reject all components, drug products, in-process materials, and procedures affecting the identity, strength, quality, and purity of the drug product.

Maintained by Gerard BlokdykVerified against the published standard Control text last updated

Other controls in Subpart B - Organization and Personnel

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