21 CFR 640.80
§ 640.80 Albumin (Human).
United States · 21 CFR — Food and Drugs · Status: effective
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- Citation
- 21 CFR 640.80, § 640.80 Albumin (Human), United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/88512
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Full text
(a) Proper name and definition. The proper name of the product shall be Albumin (Human). The product is defined as a sterile solution of the albumin derived from human plasma.
(b) Source material. The source material of Albumin (Human) shall be plasma recovered from Whole Blood prepared as prescribed in §§ 640.1 through 640.5, or Source Plasma prepared as prescribed in §§ 640.60 through 640.76.
(c) Additives in source material. Source material shall not contain an additive unless it is shown that the processing method yields a final product free of the additive to such extent that the continued safety, purity, potency, and effectiveness of the final product will not be adversely affected.
Legislative history
This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.