§ 213.22. Responsibilities of quality unit.
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/us/cfr/t21/s§ 213.22·A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
(a)There shall be a quality unit that shall have the responsibility and authority to approve or reject all components, medical gas containers and closures, in-process materials, packaging material, labeling, and medical gases, and the authority to review production records to assure that no errors have occurred or, if errors have occurred, that they have been fully investigated. The quality unit shall be responsible for approving or rejecting medical gases manufactured, processed, packed, or held under contract by another company.
(b)Adequate laboratory facilities for the testing and approval (or rejection) of components, medical gas containers and closures, packaging materials, in-process materials, and medical gases shall be available to the quality unit.
(c)The quality unit shall have the responsibility for approving or rejecting all procedures or specifications impacting on the identity, strength, quality, and purity of the medical gas.
(d)The responsibilities and procedures applicable to the quality unit shall be in writing; such written procedures shall be followed.
(e)Quality unit personnel may perform other functions provided appropriate written controls are in place to ensure any other functions are performed separately from quality unit responsibilities and such other functions do not interfere with the quality unit's responsibilities or subordinate the quality unit's responsibilities to any other unit.
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§ 213.22
Responsibilities of quality unit.
Fed. Reg.×1
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