Qtfality Control Unit Sample Clauses

Qtfality Control Unit. Drug manufacturers were required to maintain a quality control unit 'With the responsibility and authority to approve or reject all components, drugs product containers, closures, in-process materials, packaging, material, labeling and drug products and the authority to review production records to assure that no errors had occured or, if errors had occured, that they were fully investigated. 21 C.P.R. § 21 1.22(a) (2003). The quality control unit was to have the responsibility for approving or rejecting all procedures or specifications impacting on the identity, strength, quality, and purity of the drug product. 21 C.P.R. § 2 11.22(c) (2003).
Sample 1
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Related to Qtfality Control Unit

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