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21 CFR 660.52

§ 660.52 Reference preparations.

United States · 21 CFR — Food and Drugs · Status: effective

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21 CFR 660.52, § 660.52 Reference preparations, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/88569
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Reference Anti-Human Globulin preparations shall be obtained from the Food and Drug Administration, Center for Biologics Evaluation and Research, Reagents and Standards Shipping, 10903 New Hampshire Ave., Bldg. 75, Rm. G704, Silver Spring, MD 20993-0002, and shall be used as described in the accompanying package insert for determining the potency of Anti-Human Globulin.

Legislative history

This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.